RESUMO
BACKGROUND: The microvasculature (MV) of brains with Alzheimer's disease neuropathologic change (ADNC) and cerebral amyloid angiopathy (CAA), in the absence of concurrent pathologies (e.g., infarctions, Lewy bodies), is incompletely understood. OBJECTIVE: To analyze microvascular density, diameter and extracellular matrix (ECM) content in association with ADNC and CAA. METHODS: We examined samples of cerebral cortex and isolated brain microvasculature (MV) from subjects with the National Institute on Aging-Alzheimer's Association (NIA-AA) designations of not-, intermediate-, or high ADNC and from subjects with no CAA and moderate-severe CAA. Cases for all groups were selected with no major (territorial) strokes, ≤ 1 microinfarct in screening sections, and no Lewy body pathology. MV density and diameter were measured from cortical brain sections. Levels of basement membrane (BM) ECM components, the protein product of TNF-stimulated gene-6 (TSG-6), and the ubiquitous glycosaminoglycan hyaluronan (HA) were assayed by western blots or HA ELISA of MV lysates. RESULTS: We found no significant changes in MV density or diameter among any of the groups. Levels of BM laminin and collagen IV (col IV) were lower in MV isolated from the high ADNC vs. not-ADNC groups. In contrast, BM laminin was significantly higher in MV from the moderate-severe CAA vs. the no CAA groups. TSG-6 and HA content were higher in the presence of both high ADNC and CAA, whereas levels of BM fibronectin and perlecan were similar among all groups. CONCLUSIONS: Cortical MV density and diameter are not appreciably altered by ADNC or CAA. TSG-6 and HA are increased in both ADNC and CAA, with laminin and col IV decreased in the BM of high ADNC, but laminin increased in moderate-severe CAA. These results show that changes in the ECM occur in AD and CAA, but independently of one another, and likely reflect on the regional functioning of the brain microvasculature.
Assuntos
Doença de Alzheimer , Membrana Basal , Angiopatia Amiloide Cerebral , Córtex Cerebral , Matriz Extracelular , Microvasos , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/metabolismo , Doença de Alzheimer/patologia , Membrana Basal/irrigação sanguínea , Membrana Basal/metabolismo , Membrana Basal/patologia , Moléculas de Adesão Celular/metabolismo , Angiopatia Amiloide Cerebral/metabolismo , Angiopatia Amiloide Cerebral/patologia , Córtex Cerebral/irrigação sanguínea , Córtex Cerebral/metabolismo , Córtex Cerebral/patologia , Colágeno/metabolismo , Matriz Extracelular/metabolismo , Matriz Extracelular/patologia , Feminino , Humanos , Ácido Hialurônico/metabolismo , Laminina/metabolismo , Masculino , Microvasos/patologia , Bancos de TecidosRESUMO
Hypertensive intracerebral hemorrhage (ICH) is a devastating cerebrovascular disease with no effective treatment. Lysyl hydroxylase 3 (LH3) is essential for collagen IV intermolecular crosslinking and stabilization. Deficiency in LH3 affects the assembly and secretion of collagen IV and basement membrane (BM) integrity of vessels. Here, we investigated whether LH3 has significant implications for disease progression and therapeutic intervention. Spontaneous hypertensive ICH of mice was induced by angiotensin II and L-NAME treatment. The adeno-associated virus was delivered into brain by stereotactic injection to knockdown or overexpress LH3. We found LH3 levels were reduced in human patients with ICH and gradually decreased in mice before ICH. LH3 knockdown increased the incidence of hypertensive ICH in mice. The incidence, number, and size of ICHs in mice were markedly reduced by LH3 overexpression. RNA-seq revealed that LH3 overexpression significantly reversed the profound alterations in gene transcriptional profiles of cerebral vessels. LH3 overexpression was sufficient to enhance BM integrity, inhibit matrix metalloproteinase activity, attenuate microglial activation and leukocyte infiltration, and reduce VSMC apoptosis before ICH. These results indicate that LH3 overexpression attenuates susceptibility to hypertensive ICH. We emphasize that LH3 modulation may serve as a viable approach for future investigations of ICH prevention.
Assuntos
Hemorragia Intracraniana Hipertensiva/prevenção & controle , Pró-Colágeno-Lisina 2-Oxoglutarato 5-Dioxigenase/metabolismo , Animais , Membrana Basal/irrigação sanguínea , Vasos Sanguíneos/efeitos dos fármacos , Progressão da Doença , Suscetibilidade a Doenças , Humanos , Incidência , Hemorragia Intracraniana Hipertensiva/induzido quimicamente , Hemorragia Intracraniana Hipertensiva/tratamento farmacológico , Camundongos , Pró-Colágeno-Lisina 2-Oxoglutarato 5-Dioxigenase/administração & dosagem , Pró-Colágeno-Lisina 2-Oxoglutarato 5-Dioxigenase/farmacologiaRESUMO
Neural stem cells (NSCs) are retained in the adult ventricular-subventricular zone (V-SVZ), a specialized neurogenic niche with a unique cellular architecture. It currently remains unclear whether or how NSCs utilize basement membranes (BMs) in this niche. Here, we examine the molecular compositions and functions of BMs in the adult mouse V-SVZ. Whole-mount V-SVZ immunostaining revealed that fractones, which are fingerlike processes of extravascular BMs, are speckled BMs unconnected to the vasculature, and differ in their molecular composition from vascular BMs. Glial fibrillary acidic protein (GFAP)-positive astrocytes and NSCs produce and adhere to speckled BMs. Furthermore, Gfap-Cre-mediated Lamc1flox(E1605Q) knockin mice, in which integrin-binding activities of laminins are specifically nullified in GFAP-positive cells, exhibit a decreased number and size of speckled BMs and reduced in vitro neurosphere-forming activity. Our results reveal niche activities of fractones/speckled BMs for NSCs and provide molecular insights into how laminin-integrin interactions regulate NSCs in vivo.
Assuntos
Membrana Basal/metabolismo , Ventrículos Laterais/metabolismo , Células-Tronco Neurais/metabolismo , Nicho de Células-Tronco , Animais , Animais Recém-Nascidos , Membrana Basal/irrigação sanguínea , Membrana Basal/citologia , Proliferação de Células , Células Endoteliais/citologia , Células Endoteliais/metabolismo , Epêndima/citologia , Epêndima/metabolismo , Proteína Glial Fibrilar Ácida/metabolismo , Integrinas/metabolismo , Laminina/metabolismo , Ventrículos Laterais/citologia , Camundongos Endogâmicos C57BL , Mutação/genética , Células-Tronco Neurais/citologiaRESUMO
In this chapter we describe in detail the tissue processing techniques we employ for the study of cerebral tissue by transmission electron microscopy (TEM). In particular, we explain a technique that enables quantification of changes in cerebral basement membranes at the ultrastructural level. This is significant, as age related pathological conditions affecting the brain are often accompanied by ultrastructural changes in the cerebral vasculature.Briefly, experimental mice are fixed by perfusion and their brains removed. Brains are then vibratomed into 100 µm slices with regions of interest microdissected and processed for TEM following a protocol optimized for the preservation of cerebral tissue. Changes in the thickness of cerebral basement membranes are then quantified using novel software. Some prior knowledge of general TEM specimen preparation and sectioning will be useful when performing this protocol.
Assuntos
Membrana Basal/ultraestrutura , Córtex Cerebral/ultraestrutura , Microscopia Eletrônica de Transmissão/métodos , Animais , Membrana Basal/irrigação sanguínea , Córtex Cerebral/irrigação sanguínea , Dessecação/métodos , Formaldeído/química , Glutaral/química , Camundongos , Microtomia/instrumentação , Microtomia/métodos , Inclusão do Tecido/métodos , Fixação de Tecidos/métodosRESUMO
Progressive renal diseases are associated with rarefaction of peritubular capillaries, but the ultrastructural and functional alterations of the microvasculature are not well described. To study this, we analyzed different time points during progressive kidney damage and fibrosis in 3 murine models of different disease etiologies. These models were unilateral ureteral obstruction, unilateral ischemia-reperfusion injury, and Col4a3-deficient mice, we analyzed ultrastructural alterations in patient biopsy specimens. Compared with kidneys of healthy mice, we found a significant and progressive reduction of peritubular capillaries in all models analyzed. Ultrastructurally, compared with the kidneys of control mice, focal widening of the subendothelial space and higher numbers of endothelial vacuoles and caveolae were found in fibrotic kidneys. Quantitative analysis showed that peritubular capillary endothelial cells in fibrotic kidneys had significantly and progressively reduced numbers of fenestrations and increased thickness of the cell soma and lamina densa of the capillary basement membrane. Similar ultrastructural changes were also observed in patient's kidney biopsy specimens. Compared with healthy murine kidneys, fibrotic kidneys had significantly increased extravasation of Evans blue dye in all 3 models. The extravasation could be visualized using 2-photon microscopy in real time in living animals and was mainly localized to capillary branching points. Finally, fibrotic kidneys in all models exhibited a significantly greater degree of interstitial deposition of fibrinogen. Thus, peritubular capillaries undergo significant ultrastructural and functional alterations during experimental progressive renal diseases, independent of the underlying injury. Analyses of these alterations could provide read-outs for the evaluation of therapeutic approaches targeting the renal microvasculature.
Assuntos
Capilares/patologia , Células Endoteliais/patologia , Nefropatias/patologia , Túbulos Renais/irrigação sanguínea , Túbulos Renais/patologia , Animais , Membrana Basal/irrigação sanguínea , Membrana Basal/patologia , Biópsia , Capilares/ultraestrutura , Modelos Animais de Doenças , Progressão da Doença , Células Endoteliais/ultraestrutura , Fibrose , Humanos , Imuno-Histoquímica , Nefropatias/etiologia , Nefropatias/genética , Túbulos Renais/citologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Microcirculação , Microscopia Eletrônica de Varredura , Microscopia de Fluorescência por Excitação Multifotônica , Proteínas Serina-Treonina Quinases/genética , Traumatismo por Reperfusão/complicações , Fatores de Tempo , Obstrução Ureteral/complicaçõesRESUMO
COL4A1 mutations have been associated with cerebral small-vessel disease, including perinatal intracerebral hemorrhage with consequent porencephaly, microbleeds, and lacunar strokes. Moreover, involvement of multiple organs and tissues like kidney, muscle, and large vessels have been reported. Three related patients with porencephaly bearing the G749S mutation in the COL4A1 gene and one healthy control belonging to the same family underwent skin biopsy. Tissue was examined by means of immunofluorescence microscopy and immunoreactivity for collagen type IV in skin basement membranes was tested. In subjects with COL4A1 mutation, we did not detect significant alterations of immunofluorescence patterns in basal membranes of different skin structures. Heterozygous COL4A1 G749S mutation is associated with a normal immunofluorescence pattern of skin basement membranes. Further studies are needed to clarify the role of possible functional abnormalities of the basement membranes in patients with this mutation.
Assuntos
Membrana Basal/patologia , Colágeno Tipo IV/metabolismo , Mutação , Porencefalia/genética , Porencefalia/patologia , Adulto , Membrana Basal/irrigação sanguínea , Membrana Basal/inervação , Membrana Basal/metabolismo , Colágeno Tipo IV/genética , Família , Feminino , Imunofluorescência , Humanos , Masculino , Microscopia Confocal , Pessoa de Meia-Idade , Porencefalia/metabolismo , Glândulas Sebáceas/metabolismo , Glândulas Sebáceas/patologia , Adulto JovemRESUMO
OBJECTIVE: In a proportion of patients with preeclampsia, unremodeled spiral arteries develop additional pathological changes, termed decidual vasculopathy (DV), or acute atherosis. DV has been correlated to adverse clinical outcome and increased placental pathology. However, it was unclear whether these effects pertained to individual features of DV. METHODS: We performed a reanalysis of placental samples from preeclamptic pregnancies (n = 76), recording the number of vessels with DV, their location in the decidua and their morphological features. Results were correlated with clinical and placental parameters, using Spearman's rho test. P-value < 0.05 was considered significant. RESULTS: Total number of vessels with DV (totalDV) correlated with higher diastolic blood pressure, higher urine protein-to-creatinine ratio, shorter gestational age, lower birth weight, 5 min APGAR score and umbilical artery pH, and with increased accelerated villous maturity, infarction and hematoma formation, but not with HELLP syndrome markers. Additionally, there was a striking correlation of increased perinatal mortality with the number of vessels located in the decidua basalis (DVbas), and with vessels showing DV with thrombosis (DVthrom). Other morphological features, such as foam cell infiltration, did not increase correlation strength. DISCUSSION: In our study of preeclamptic placental samples, totalDV related to worse clinical outcome and increased placental pathology. Moreover, DVbas and DVthrom related to perinatal death. DV could be a manifestation of an underlying (vascular) pathology, increasing the risk of adverse pregnancy outcome. CONCLUSIONS: In preeclampsia, totalDV, DVbas and DVthrom correlated with increased placental pathology and adverse maternal and fetal outcome, most relevantly with perinatal mortality.
Assuntos
Decídua/irrigação sanguínea , Pré-Eclâmpsia/patologia , Doenças Vasculares/etiologia , Adulto , Membrana Basal/irrigação sanguínea , Membrana Basal/imunologia , Membrana Basal/patologia , Peso ao Nascer , Decídua/imunologia , Decídua/patologia , Feminino , Células Espumosas/imunologia , Células Espumosas/patologia , Humanos , Recém-Nascido , Ativação de Macrófagos , Masculino , Países Baixos/epidemiologia , Mortalidade Perinatal , Placenta/irrigação sanguínea , Placenta/imunologia , Placenta/patologia , Pré-Eclâmpsia/imunologia , Pré-Eclâmpsia/mortalidade , Pré-Eclâmpsia/fisiopatologia , Gravidez , Resultado da Gravidez , Nascimento Prematuro/etiologia , Proteinúria/etiologia , Estudos Retrospectivos , Índice de Gravidade de Doença , Trombose/etiologiaRESUMO
Perlecan is a heparan sulfate proteoglycan assembled into the vascular basement membranes (BMs) during vasculogenesis. In the present study we have investigated vessel formation in mice, teratomas and embryoid bodies (EBs) in the absence of perlecan. We found that perlecan was dispensable for blood vessel formation and maturation until embryonic day (E) 12.5. At later stages of development 40% of mutant embryos showed dilated microvessels in brain and skin, which ruptured and led to severe bleedings. Surprisingly, teratomas derived from perlecan-null ES cells showed efficient contribution of perlecan-deficient endothelial cells to an apparently normal tumor vasculature. However, in perlecan-deficient EBs the area occupied by an endothelial network and the number of vessel branches were significantly diminished. Addition of FGF-2 but not VEGF(165) rescued the in vitro deficiency of the mutant ES cells. Furthermore, in the absence of perlecan in the EB matrix lower levels of FGFs are bound, stored and available for cell surface presentation. Altogether these findings suggest that perlecan supports the maintenance of brain and skin subendothelial BMs and promotes vasculo- and angiogenesis by modulating FGF-2 function.
Assuntos
Proteoglicanas de Heparan Sulfato/fisiologia , Microvasos/embriologia , Microvasos/fisiologia , Neovascularização Fisiológica , Animais , Membrana Basal/irrigação sanguínea , Membrana Basal/embriologia , Encéfalo/irrigação sanguínea , Encéfalo/embriologia , Corpos Embrioides/citologia , Corpos Embrioides/fisiologia , Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/fisiologia , Feminino , Fator 2 de Crescimento de Fibroblastos/fisiologia , Proteoglicanas de Heparan Sulfato/deficiência , Proteoglicanas de Heparan Sulfato/genética , Camundongos , Camundongos da Linhagem 129 , Camundongos Endogâmicos C57BL , Camundongos Knockout , Microvasos/ultraestrutura , Neovascularização Patológica , Gravidez , Pele/irrigação sanguínea , Pele/embriologia , Teratoma/irrigação sanguíneaRESUMO
PURPOSE: Basal lamina is a major part of the microvascular wall and plays a critical role in the integrity of microvasculature. The aim of this study is to determine whether hyperthermia worsens the destruction of microvascular integrity in the ischaemic injured brain. MATERIALS AND METHODS: Focal cerebral ischaemia was induced by embolising a pre-formed clot into the middle cerebral artery (MCA). Rats received either normothermic or hyperthermic treatment. Neurological score and infarct size were evaluated at 24 h after the MCA occlusion. Microvascular collagen type IV and laminin were measured with fluorescence microscopy. The activities of matrix metalloproteinases (MMP-2 and MMP-9) and plasminogen activators (tPA and uPA) were determined by zymography. RESULTS: Treatment with hyperthermia significantly increased infarct volume (p<0.01), cortex swelling (p<0.01), striatum swelling (p<0.05) and neurologic score (p<0.01) at 24 h after the MCA occlusion. Compared to the normothermic groups, hyperthermia significantly worsened the losses of microvascular basal lamina structure proteins, collagen type IV and laminin, at 6 h (p<0.001) and 24 h (p<0.01) after MCA occlusion. Hyperthermia increased the MMP-9 activity at 6 and 24 h after MCA occlusion compared with normothermia (p<0.05), whereas increased the MMP-2 activity at 6 h only (p<0.05). Hyperthermia also elevated uPA activity significantly at 6 and 24 h after MCA occlusion compared to normothermia (p<0.05). CONCLUSIONS: These results demonstrate that hyperthermia exacerbates the destruction of microvascular integrity possibly by increasing the activities of MMP-2, MMP-9 and uPA in the ischaemic cerebral tissues.
Assuntos
Membrana Basal/irrigação sanguínea , Infarto Encefálico/patologia , Isquemia Encefálica/patologia , Hipertermia Induzida/efeitos adversos , Microvasos/patologia , Animais , Membrana Basal/patologia , Comportamento Animal , Infarto Encefálico/fisiopatologia , Isquemia Encefálica/fisiopatologia , Córtex Cerebral/irrigação sanguínea , Córtex Cerebral/patologia , Colágeno Tipo IV/metabolismo , Corpo Estriado/irrigação sanguínea , Corpo Estriado/patologia , Modelos Animais de Doenças , Laminina/metabolismo , Masculino , Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Ativadores de Plasminogênio/metabolismo , Ratos , Ratos Sprague-DawleyRESUMO
The blood-follicle barrier (BFB) is one of the blood-tissue barriers in mammalian body found in developing follicles in the ovary. The BFB, besides the tight junction (TJ)-permeability barrier of the endothelial cells in the microvessels that surround the developing follicle, is constituted and contributed significantly by the basement membrane of the developing follicle which alters its composition rapidly during follicle development. While the concept of the BFB and its ultrastructure were described more than six decades ago, fewer than 20 reports are found in the literature that were dedicated to investigate the biology, regulation, and function of the BFB either in health or in disease. Furthermore, detailed analysis of the adhesion protein complexes and the regulation of the junction dynamics at the BFB are still missing in the literature. The goal of this short chapter is to provide an update on this important blood-tissue barrier, it is obvious that future investigation is much needed in the field to understand this ultrastructure better in order to treat and better ovarian disorders including ovarian cancer.
Assuntos
Folículo Ovariano/patologia , Folículo Ovariano/fisiologia , Neoplasias Ovarianas/metabolismo , Síndrome do Ovário Policístico/metabolismo , Animais , Membrana Basal/irrigação sanguínea , Membrana Basal/metabolismo , Transporte Biológico , Permeabilidade da Membrana Celular , Endotélio Vascular/metabolismo , Endotélio Vascular/patologia , Feminino , Líquido Folicular/metabolismo , Humanos , Imunoquímica , Folículo Ovariano/irrigação sanguínea , Neoplasias Ovarianas/patologia , Síndrome do Ovário Policístico/irrigação sanguínea , Síndrome do Ovário Policístico/patologia , Junções Íntimas/patologiaRESUMO
BACKGROUND AND OBJECTIVE: To present spectral domain optical coherence tomography (SD-OCT), scanning laser ophthalmoscopy, and intraoperative images showing possible pathways of blood entrance into the eye and ways in which it may spread inside the eye in Terson syndrome. PATIENTS AND METHODS: Nine eyes of 5 patients with Terson syndrome underwent pars plana vitrectomy. Surgeries were recorded and analyzed afterward. SD-OCT and scanning laser ophthalmoscopy examinations were performed after surgery. RESULTS: Visual acuity improved in all cases. SD-OCT three-dimensional mode improved visualization of the internal limiting membrane (ILM), possibly due to sub-ILM blood spreading detachment near the macula and optic disc. Scanning laser ophthalmoscopy revealed blood spreading along vessels and blood under the retina was observed intraoperatively. CONCLUSION: SD-OCT, scanning laser ophthalmoscopy, and intraoperative images show that blood may enter the vitreous cavity around the retinal vessels near the optic disc. Inside the eye, the blood may spread intraretinally, sub-ILM, or along the retinal vessels.
Assuntos
Hematoma Subdural/etiologia , Hemorragia Subaracnóidea/etiologia , Corpo Vítreo/irrigação sanguínea , Hemorragia Vítrea/diagnóstico , Adulto , Membrana Basal/irrigação sanguínea , Feminino , Humanos , Período Intraoperatório , Masculino , Pessoa de Meia-Idade , Oftalmoscopia , Fluxo Sanguíneo Regional , Vasos Retinianos/patologia , Líquido Sub-Retiniano , Síndrome , Tomografia de Coerência Óptica , Acuidade Visual/fisiologia , Vitrectomia , Hemorragia Vítrea/fisiopatologia , Hemorragia Vítrea/cirurgia , Adulto JovemRESUMO
PURPOSE: The purpose of this study was to determine the histopathologic characteristics of bevacizumab-treated human proliferative diabetic retinopathy (PDR) membranes with particular regard to membrane vasculature as a step toward addressing the effects of the drug on PDR membranes. Intravitreous injection of bevacizumab, an antivascular endothelial growth factor monoclonal antibody, has recently been advocated as an adjunct in surgery for PDR. In this context, a clinically observed decrease in PDR epiretinal membrane vascularity (vascular regression) occurs from 24 hours to 48 hours after injection, but the exact mechanisms of drug action are unknown. METHODS: A consecutive series of seven PDR membrane specimens that had been removed sequentially from seven bevacizumab-treated patients were studied retrospectively. The membrane specimens were examined using light microscopic methods, including immunohistochemistry. RESULTS: Five of the seven membranes were clinically avascular (one contained "ghost" vessels) and did not hemorrhage during excision. Of these 5 specimens, which included 1 removed 7 days after a total of 6 intravitreous injections of 1.25 mg bevacizumab, 4 contained histologically detectable capillaries (1 did not). These blood vessels were lined by endothelial cells as determined by immunohistochemistry for the endothelial markers CD31 and CD34. The two remaining membranes were clinically and histologically still vascularized despite bevacizumab treatment. All the specimens also contained smooth muscle actin-containing fibroblastic cells within the collagenous stroma. CONCLUSION: The findings do not support the concept that the clinical phenomenon of vascular regression in PDR membranes after bevacizumab injection in the vitreous is resulting from obliteration of the membrane blood vessels. Another mechanism appears to be involved in at least some patients, possibly a vasoconstrictive response. Such a mechanism might explain reversal of the effects of bevacizumab that has been reported after this treatment.
Assuntos
Inibidores da Angiogênese/administração & dosagem , Anticorpos Monoclonais/administração & dosagem , Membrana Basal/patologia , Retinopatia Diabética/tratamento farmacológico , Neovascularização Retiniana/tratamento farmacológico , Fator A de Crescimento do Endotélio Vascular/antagonistas & inibidores , Actinas/metabolismo , Adulto , Idoso , Anticorpos Monoclonais Humanizados , Antígenos CD34/metabolismo , Membrana Basal/irrigação sanguínea , Bevacizumab , Retinopatia Diabética/metabolismo , Retinopatia Diabética/patologia , Feminino , Fibrose , Humanos , Técnicas Imunoenzimáticas , Injeções , Masculino , Pessoa de Meia-Idade , Molécula-1 de Adesão Celular Endotelial a Plaquetas/metabolismo , Neovascularização Retiniana/metabolismo , Neovascularização Retiniana/patologia , Estudos Retrospectivos , Acuidade Visual , Corpo VítreoRESUMO
OBJECTIVE: To explore the protective effects of rhubarb aglycone combined with urokinase (UK) thrombolysis on brain microvascular basement membrane impairment in rats with thrombus-occluded cerebral ischemia by regulating the expression of IgG, CoLIV and LN in rats brain, by which the level of injury of brain microvascular basement membrane could be detected. METHOD: Rats were randomly divided into sham-operated, model, thrombolysis, rhubarb aglycone and combination (rhubarb aglycone combined with thrombolysis) groups. Moreover, rats in model, thrombolysis, rhubarb aglycone and combination groups were randomly divided into 3, 6, and 9 h groups respectively. Model of thrombus-occluded cerebral ischemia was duplicated by using the combination of rats' auto-thrombus with inserting the nylon thread. Rats were administrated with thrombolysis therapy through artery at 3, 6, and 9 h after cerebral ischemia. At 24 h of administration through artery, intracranial hemorrhage ratio (ICHR) and mortality of rats were observed, and then the brain of rats was taken. In the study, expression of IgG, CoLIV and LN in rats brain were measured. RESULT: Thrombolysis at 9 h of cerebral ischemia made rats mortality and BHR increase, administration of combined therapy could make them decrease. Expression of IgG level in rats brain of 9 h and 6 h model groups increased, while CoLIV and LN expression decreased significantly. In each administration 9 h group, IgG level was lower, and CoLIV and LN were higher, such changes appeared significantly in rhubarb aglycone and association groups. CONCLUSION: Brain microvascular basement membrane impairment could be caused by the therapy of delayed thrombolysis, which made the mortality and BHR increase. Rhubarb aglycone combined with the therapy of thrombolysis could perform the protective effects on brain microvascular basement membrane and then decrease the ICHR and mortality caused by thrombolysis after cerebral ischemia.
Assuntos
Membrana Basal/irrigação sanguínea , Isquemia Encefálica/tratamento farmacológico , Medicamentos de Ervas Chinesas/uso terapêutico , Trombose Intracraniana/tratamento farmacológico , Rheum/química , Terapia Trombolítica , Ativador de Plasminogênio Tipo Uroquinase/uso terapêutico , Animais , Membrana Basal/efeitos dos fármacos , Isquemia Encefálica/mortalidade , Modelos Animais de Doenças , Quimioterapia Combinada , Feminino , Humanos , Trombose Intracraniana/mortalidade , Masculino , Distribuição Aleatória , Ratos , Ratos Sprague-DawleyRESUMO
Mast cells (MCs) are multifunctional effectors of the immune system that are distributed in many tissues, often in close association with the basement membrane of blood vessels, epithelium and nerves. Laminins (LMs), a family of large alphabetagamma heterotrimeric proteins, are major components of basement membrane that strongly promote cell adhesion and migration. In this study, we investigated the role of LM isoforms and their integrin receptors in human MC biology in vitro. In functional assays, alpha3-(LM-332) and alpha5-(LM-511) LMs, but not alpha1-(LM-111), alpha2-(LM-211), or alpha4-(LM-411) LMs, readily promoted adhesion and migration of cultured MCs. These activities were strongly enhanced by various stimuli. alpha3-LM was also able to costimulate IL-8 production. Among LM-binding integrins, MCs expressed alpha(3)beta(1), but not alpha(6)beta(1), alpha(7)beta(1), or alpha(6)beta(4), integrins. Blocking Abs to alpha(3)beta(1) integrin caused inhibition of both cell adhesion and migration on alpha3- and alpha5-LMs. Immunohistochemical studies on skin showed that MCs colocalized with epithelial and vascular basement membranes that expressed alpha3- and alpha5-LMs and that MCs expressed alpha(3) integrin but not alpha(6) integrin(s). These results demonstrate a role for alpha3- and alpha5-LMs and their alpha(3)beta(1) integrin receptor in MC biology. This may explain the intimate structural and functional interactions that MCs have with specific basement membranes.
Assuntos
Membrana Basal/irrigação sanguínea , Membrana Basal/metabolismo , Movimento Celular , Sangue Fetal/citologia , Sangue Fetal/metabolismo , Integrina alfa3beta1/fisiologia , Laminina/fisiologia , Mastócitos/metabolismo , Idoso , Idoso de 80 Anos ou mais , Membrana Basal/imunologia , Adesão Celular/imunologia , Linhagem Celular , Movimento Celular/imunologia , Feminino , Sangue Fetal/imunologia , Humanos , Integrina alfa3beta1/sangue , Laminina/sangue , Masculino , Mastócitos/citologia , Mastócitos/imunologia , Pessoa de Meia-Idade , Isoformas de Proteínas/sangue , Isoformas de Proteínas/fisiologiaRESUMO
PURPOSE: Alterations in FOXC1 dosage lead to a spectrum of highly penetrant, ocular anterior segment dysgenesis phenotypes. The most serious outcome is the development of glaucoma, which occurs in 50% to 75% of patients. Therefore, the need to identify specific pathways and genes that interact with FOXC1 to promote glaucoma is great. In this study, the authors investigated the loss of foxC1 in the zebrafish to characterize phenotypes and gene interactions that may impact glaucoma pathogenesis. METHODS: Morpholino knockdown in zebrafish, RNA and protein marker analyses, transgenic reporter lines, and angiography, along with histology and transmission electron microscopy, were used to study foxC1 function and gene interactions. RESULTS: Zebrafish foxC1 genes were expressed dynamically in the developing vasculature and periocular mesenchyme during development. Multiple ocular and vascular defects were found after the knockdown of foxC1. Defects in the hyaloid vasculature, arteriovenous malformations, and coarctation of the aorta were observed with maximal depletion of foxC1. Partial loss of foxC1 resulted in CNS and ocular hemorrhages, defects in intersegmental vessel patterning, and increased vascular permeability. To investigate the basis for these disruptions, the ultrastructure of foxC1-depleted hyaloid vascular cells was studied. These experiments, along with laminin-111 immunoreactivity, revealed disruptions in basement membrane integrity. Finally, codepletion of laminin alpha-1 and foxC1 uncovered a genetic interaction between these genes during development. CONCLUSIONS: Genetic interactions between FOXC1 and basement membrane components influence vascular stability and may impact glaucoma development and increase stroke risk in FOXC1 patients.
Assuntos
Membrana Basal/irrigação sanguínea , Endotélio Vascular/metabolismo , Fatores de Transcrição Forkhead/fisiologia , Morfogênese/fisiologia , Artéria Oftálmica/embriologia , Proteínas de Peixe-Zebra/fisiologia , Peixe-Zebra/embriologia , Animais , Membrana Basal/metabolismo , Membrana Basal/patologia , Biomarcadores/metabolismo , Endotélio Vascular/patologia , Olho/embriologia , Angiofluoresceinografia , Técnica Indireta de Fluorescência para Anticorpo , Expressão Gênica , Técnicas de Inativação de Genes , Inativação Gênica , Hibridização In Situ , Laminina/metabolismo , Cristalino/irrigação sanguínea , Microscopia Confocal , Microscopia Eletrônica de Transmissão , Artéria Oftálmica/metabolismo , Artéria Oftálmica/patologia , Proteínas de Peixe-Zebra/metabolismoAssuntos
Corpo Ciliar/irrigação sanguínea , Corpo Ciliar/cirurgia , Fotocoagulação a Laser/efeitos adversos , Neovascularização Patológica/etiologia , Membrana Basal/irrigação sanguínea , Evolução Fatal , Glaucoma Neovascular/cirurgia , Humanos , Pressão Intraocular , Masculino , Pessoa de Meia-Idade , Acuidade VisualRESUMO
The polysaccharide heparan sulphate is ubiquitously expressed as a proteoglycan in extracellular matrices and on cell surfaces. Heparan sulphate has marked sequence diversity that allows it to specifically interact with many proteins. This Review focuses on the multiple roles of heparan sulphate in inflammatory responses and, in particular, on its participation in almost every stage of leukocyte transmigration through the blood-vessel wall. Heparan sulphate is involved in the initial adhesion of leukocytes to the inflamed endothelium, the subsequent chemokine-mediated transmigration through the vessel wall and the establishment of both acute and chronic inflammatory reactions.
Assuntos
Heparitina Sulfato/imunologia , Heparitina Sulfato/metabolismo , Animais , Membrana Basal/irrigação sanguínea , Membrana Basal/metabolismo , Adesão Celular , Quimiocinas/imunologia , Quimiocinas/metabolismo , Humanos , Inflamação/imunologia , Inflamação/metabolismo , Inflamação/patologia , Inflamação/terapia , Proteoglicanas/imunologia , Proteoglicanas/metabolismoRESUMO
Lichen planus is a dermatologic disease of unknown etiology characterized by keratotic plaques on the skin. Many patients also harbor white lesions of the oral mucosa. The literature contains numerous reports of lichen planus-like lesions evolving in conjunction with the administration of a variety of pharmacologic agents. It is difficult, if not impossible, to distinguish such lesions from one another. The present study evaluated the epithelial and basement membrane thickness, mast cells (intact cells and degranulated cells subepithelially) and the presence or absence of blood vessels in oral lichen planus and oral lichenoid lesions. The evaluation was done using the periodic acid-schiff (PAS) and toluidine blue staining techniques on 20 cases each of oral lichen planus and oral lichenoid lesions and 5 control specimens of normal buccal mucosa. The results showed an increased number of degranulated mast cells in areas of basement membrane degeneration, increased vascularity and increased PAS-positive basement membrane thickness in oral lichen planus as compared with oral lichenoid lesions. Reduced epithelial thickness was found in oral lichen planus. The present study emphasizes the importance of these parameters in differentiating oral lichen planus from oral lichenoid lesions using special staining techniques.
Assuntos
Líquen Plano Bucal/patologia , Adolescente , Adulto , Membrana Basal/irrigação sanguínea , Membrana Basal/patologia , Estudos de Casos e Controles , Degranulação Celular , Corantes , Diagnóstico Diferencial , Células Epiteliais/patologia , Feminino , Humanos , Erupções Liquenoides/patologia , Masculino , Mastócitos/patologia , Pessoa de Meia-Idade , Reação do Ácido Periódico de Schiff , Estatísticas não Paramétricas , Cloreto de TolônioRESUMO
BACKGROUND: There is increasing in vitro evidence to support a role for vascular endothelial growth factor (VEGF), a major regulator of angiogenesis, as a mediator of fibrosis associated with neovascularization. OBJECTIVE: We tested the hypothesis that VEGF is involved both in increased airway mucosal vascularity and in the subepithelial fibrosis of asthmatic patients. METHODS: Bronchial biopsies were performed in 24 asthmatic patients and eight healthy controls. Immunostaining, using computerized image analysis, was performed using monoclonal antibodies against VEGF(+) cells, type IV collagen, to outline the basement membrane thickness, and tryptase and EG2, to identify mast cells and eosinophils, respectively. RESULTS: The counts of VEGF(+) cells (P<0.05), mast cells and EG2(+) cells (both P<0.01) were higher in asthmatics than in controls. The number of vessels, the vascular area in the lamina propria, and the basement membrane thickness were significantly higher in asthmatics than in healthy volunteers (P<0.01). Moreover, in asthmatic patients, the number of VEGF(+) cells was significantly related to the number of vessels (P<0.01), to mast cells (P<0.01) and to basement membrane thickness (P<0.01). A colocalization study also revealed that mast cells were a relevant cellular source of VEGF. High doses of inhaled fluticasone propionate significantly reduced VEGF(+) cells (P<0.05), vessel number (P<0.05), vascular area (P<0.05) and basement membrane thickness (P<0.05) in a subgroup of asthmatic patients. CONCLUSIONS: This study shows that VEGF, in addition to being involved in the vascular component of airway remodelling, may play a role in the thickening of the basement membrane in asthma.