RESUMO
We report a singular case of pigmented pagetoid Bowen's disease showing transitional features between extramammary Paget's disease and in situ squamous cell carcinoma.^ieng
Differentiation of pagetoid cutaneous neoplasms can be very challenging on hematoxylin and eosin-stained sections.
Assuntos
Adenocarcinoma in Situ/diagnóstico , Doença de Bowen/diagnóstico , Neoplasias Cutâneas/diagnóstico , Adenocarcinoma in Situ/patologia , Idoso , Doença de Bowen/patologia , Diagnóstico Diferencial , Feminino , Humanos , Neoplasias Cutâneas/patologiaRESUMO
STUDY DESIGN: Cell transplantation strategies are gaining increasing interest for spinal cord injury (SCI) with the objective of promoting spinal cord repair. To avoid allogenic graft rejection, an adequate immune suppression is required, and one of the most potent and commonly used immunosuppressives is cyclosporin A (CsA). In SCI, permanent sensory motor loss is combined with modifications of drug absorption, distribution and elimination. OBJECTIVES: The objectives of this study were to thoroughly explore histological and functional outcomes of CsA treatment in a rat model of spinal cord compression. SETTING: Experiments were carried out at the Institute for Neurosciences of Montpellier (France), the Integrative Biology of Neurodegeneration Laboratory (Spain) and in the Novartis Institutes for BioMedical Research (Switzerland) for CsA blood concentration determination. METHODS: We first evaluated histological outcomes of CsA treatment on kidneys and spinal cord after SCI. We then investigated whether SCI modified CsA blood concentration. Finally, using behavioral analysis, we assessed the potential CsA impact on functional recovery. RESULTS: When spinal-cord-injured rats were treated with a CsA dose of 10 mg kg(-1) per day, we observed deleterious effects on kidneys, associated with modifications of CsA blood concentration. Adding an antibiotic treatment reduced kidney alteration without modifying CsA blood concentration. Finally, we showed that CsA treatment per se modified neither functional recovery nor lesion extension. CONCLUSION: This study pinpoints the absolute requirement of careful CsA monitoring in the clinical setting for patients with SCI to minimize potential unexpected effects and avoid therapeutic failure.
Assuntos
Transplante de Células/métodos , Ciclosporina/toxicidade , Rejeição de Enxerto/tratamento farmacológico , Nefropatias/fisiopatologia , Traumatismos da Medula Espinal/fisiopatologia , Animais , Transplante de Células/efeitos adversos , Ciclosporina/sangue , Ciclosporina/uso terapêutico , Modelos Animais de Doenças , Quimioterapia Combinada/métodos , Rejeição de Enxerto/fisiopatologia , Rejeição de Enxerto/prevenção & controle , Imunossupressores/sangue , Imunossupressores/uso terapêutico , Imunossupressores/toxicidade , Nefropatias/induzido quimicamente , Masculino , Ratos , Ratos Wistar , Traumatismos da Medula Espinal/cirurgia , Resultado do TratamentoRESUMO
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein expressed predominantly in astrocytes. The study of its expression in the astrocyte lineage during development and in reactive astrocytes has revealed an intricate relationship with the expression of vimentin, another intermediate filament protein widely expressed in embryonic development. these findings suggested that vimentin could be implicated in the organization of the GFAP network. To address this question, we have examined GFAP expression and network formation in the recently generated vimentin knockout (Vim-) mice. We show that the GFAP network is disrupted in astrocytes that normally coexpress vimentin and GFAP, e.g., those of the corpus callosum or the Bergmann glia of cerebellum. Furthermore, Western blot analysis of GFAP protein content in the cerebellum suggests that posttranslational mechanisms are implicated in the disturbance of GFAP network formation. The role of vimentin in this process was further suggested by transfection of Vim-cultured astrocytes with a vimentin cDNA, which resulted in the normal assembly of the GFAP network. Finally, we examined GFAP expression after stab wound-induced astrogliosis. We demonstrate that in Vim- mice, reactive astrocytes that normally express both GFAP and vimentin do not exhibit GFAP immunoreactivity, whereas those that normally express GFAP only retain GFAP immunoreactivity. Taken together, these results show that in astrocytes, where vimentin is normally expressed with GFAP fails to assemble into a filamentous network in the absence of vimentin. In these cells, therefore, vimentin appears necessary to stabilize GFAP filaments and consequently the network formation.
Assuntos
Astrócitos/metabolismo , Proteína Glial Fibrilar Ácida/biossíntese , Vimentina/fisiologia , Animais , Astrócitos/citologia , Astrócitos/ultraestrutura , Sequência de Bases , Lesões Encefálicas/metabolismo , Células Cultivadas , Primers do DNA , Proteína Glial Fibrilar Ácida/ultraestrutura , Humanos , Filamentos Intermediários/metabolismo , Filamentos Intermediários/ultraestrutura , Camundongos , Camundongos Knockout , Dados de Sequência Molecular , Transfecção , Vimentina/deficiência , Vimentina/genéticaRESUMO
Traumatic lesions of the spinal cord yield a loss of supraspinal control of voluntary locomotor activity, although the spinal cord contains the necessary circuitry to generate the basic locomotor pattern. In spinal rats, this network, known as central pattern generator (CPG), was shown to be sensitive to serotonergic pharmacological stimulation. In previous works we have shown that embryonic raphe cells transplanted into the sublesional cord of adult rats can reinnervate specific targets, restore the lesion-induced increase in receptor densities of neurotransmitters, promote hindlimb weight support, and trigger a locomotor activity on a treadmill without any other pharmacological treatment or training. With the aim of discriminating whether the action of serotonin on CPG is associated to a specific level of the cord, we have transplanted embryonic raphe cells at two different levels of the sublesional cord (T9 and T11) and then performed analysis of the kinematic and EMG activity synchronously recorded during locomotion. Locomotor performances were correlated to the reinnervated level of the cord and compared to that of intact and transected nontransplanted animals. The movements expressed by T11 transplanted animals correspond to a well defined locomotor pattern comparable to that of the intact animals. On the contrary, T9 transplanted animals developed limited and disorganized movements as those of nontransplanted animals. The correlation of the locomotor performances with the level of reinnervation of the spinal cord suggests that serotonergic reinnervation of the L1-L2 level constitutes a key element in the genesis of this locomotor rhythmic activity. This is the first in vivo demonstration that transplanted embryonic raphe cells reinnervating a specific level of the cord activate a locomotor behavior.
Assuntos
Transplante de Tecido Encefálico/fisiologia , Transplante de Tecido Fetal/fisiologia , Locomoção/fisiologia , Atividade Motora/fisiologia , Núcleos da Rafe/citologia , Traumatismos da Medula Espinal/fisiopatologia , Traumatismos da Medula Espinal/cirurgia , Medula Espinal/fisiopatologia , Animais , Fenômenos Biomecânicos , Eletromiografia , Feminino , Vértebras Lombares , Músculo Esquelético/inervação , Ratos , Ratos Sprague-Dawley , Medula Espinal/fisiologiaRESUMO
Intermediate filaments (IFs) are a major component of the cytoskeleton in astrocytes. Their role is far from being completely understood. Immature astrocytes play a major role in neuronal migration and neuritogenesis, and their IFs are mainly composed of vimentin. In mature differentiated astrocytes, vimentin is replaced by the IF protein glial fibrillary acidic protein (GFAP). In response to injury of the CNS in the adult, astrocytes become reactive, upregulate the expression of GFAP, and reexpress vimentin. These modifications contribute to the formation of a glial scar that is obstructive to axonal regeneration. Nevertheless, astrocytes in vitro are considered to be the ideal substratum for the growth of embryonic CNS axons. In the present study, we have examined the potential role of these two major IF proteins in both neuronal survival and neurite growth. For this purpose, we cocultured wild-type neurons on astrocytes from three types of knock-out (KO) mice for GFAP or/and vimentin in a neuron-astrocyte coculture model. We show that the double KO astrocytes present many features of immaturity and greatly improve survival and neurite growth of cocultured neurons by increasing cell-cell contact and secreting diffusible factors. Moreover, our data suggest that the absence of vimentin is not a key element in the permissivity of the mutant astrocytes. Finally, we show that only the absence of GFAP is associated with an increased expression of some extracellular matrix and adhesion molecules. To conclude, our results suggest that GFAP expression is able to modulate key biochemical properties of astrocytes that are implicated in their permissivity.
Assuntos
Proteína Glial Fibrilar Ácida/biossíntese , Proteínas do Tecido Nervoso , Moléculas de Adesão de Célula Nervosa/biossíntese , Neuritos/metabolismo , Neurônios/metabolismo , Vimentina/biossíntese , Animais , Astrócitos/metabolismo , Astrócitos/ultraestrutura , Caderinas/metabolismo , Adesão Celular/fisiologia , Contagem de Células , Sobrevivência Celular/genética , Células Cultivadas , Técnicas de Cocultura , Matriz Extracelular/metabolismo , Fibronectinas/metabolismo , Marcação de Genes , Proteína Glial Fibrilar Ácida/deficiência , Proteína Glial Fibrilar Ácida/genética , Proteínas de Filamentos Intermediários/biossíntese , Filamentos Intermediários/metabolismo , Filamentos Intermediários/ultraestrutura , Camundongos , Camundongos Endogâmicos , Camundongos Knockout , Modelos Biológicos , Nestina , Moléculas de Adesão de Célula Nervosa/metabolismo , Neuritos/ultraestrutura , Neurônios/citologia , Vimentina/deficiência , Vimentina/genéticaRESUMO
Transection of the spinal cord yields a permanent deficit due to the interruption of descending and ascending tracts which subserve the supraspinal control of spinal cord functions. We have shown previously that transplantation below the level of the section of embryonic monoaminergic neurons can promote the recovery of some segmental functions via a local serotonergic and noradrenergic reinnervation. Moreover, the up-regulation of the corresponding receptors resulting from the section was corrected by the transplants. The aim of the present work was to determine whether such a graft could also influence non-monoaminergic local neurons, the GABAergic interneurons of the spinal cord. Following spinal cord transection, the number of cells which express glutamate decarboxylase (mol. wt 67,000) messenger RNA--a marker of GABA synthesis--increased significantly below the lesion compared with the intact animal. In contrast, in lesioned animals which had been grafted one week later with raphe neuroblasts, this number was close to control level. These post-grafting modifications were further associated with increased GABA immunoreactivity in the host tissue. These data suggest that the graft of embryonic raphe cells which compensates the deficit of serotonin in the distal segment also regulates the expression of the GABAergic phenotype in the host spinal cord. This regulation could be mediated by the re-establishment of a local functional innervation by both serotonin and GABAergic transplanted neurons and/or by trophic factors released from the embryonic cells. It appears then that grafted cells influence the host tissue in a complex manner, through the release and/or regulation of several neurotransmitter systems.
Assuntos
Transplante de Células , Transplante de Tecido Fetal , Núcleos da Rafe/embriologia , Traumatismos da Medula Espinal/fisiopatologia , Traumatismos da Medula Espinal/cirurgia , Ácido gama-Aminobutírico/metabolismo , Animais , Embrião de Mamíferos/citologia , Feminino , Imuno-Histoquímica , Hibridização In Situ , Interneurônios/fisiologia , Fenótipo , Núcleos da Rafe/citologia , Ratos , Ratos Sprague-Dawley , Medula Espinal/metabolismo , Traumatismos da Medula Espinal/genética , Traumatismos da Medula Espinal/patologiaRESUMO
Treatment of neurodegenerative diseases by classical pharmacotherapy is restricted by blood-brain barrier which prevents access to the brain of potentially therapeutic molecules. Recent progress in the knowledge of pathophysiological molecular processes, and in the development of molecular biotechnology have opened the way to new therapeutic interventions for these disorders. This chapter reviews the most recent gene therapy strategies using experimental models for neurodegenerative diseases.
Assuntos
Terapia Genética/métodos , Doenças Neurodegenerativas/terapia , Doença de Alzheimer/terapia , Esclerose Lateral Amiotrófica/terapia , Animais , Surdez/terapia , Vetores Genéticos , Humanos , Doença de Huntington/terapia , Neurônios , Doença de Parkinson/terapia , Transtornos Parkinsonianos/terapia , Regiões Promotoras Genéticas , Retinose Pigmentar/terapiaRESUMO
A great deal of interest has attracted the attention of researchers on the potential use of (neural) stem cells in cell replacement or restorative therapies for heretofore incurable CNS pathologies such as brain stroke, spinal cord injury, Parkinson's disease or multiple sclerosis. This short perspective illustrates our view of neural stem cell research with a focus on the stem cell concept, on the in situ identity of neural stem cells and on selected aspects of embryonic and adult neurogenesis. A brief survey of current stem cell-based experimental literature tries to provide a realistic picture of how far we have gone in the quest to establish a restorative neurology.
Assuntos
Neurologia , Neurônios/citologia , Células-Tronco/citologia , Animais , Diferenciação Celular , Humanos , Esclerose Múltipla/terapia , Doença de Parkinson/terapia , Pesquisa , Traumatismos da Medula Espinal/terapia , Acidente Vascular Cerebral/terapiaRESUMO
Severe traumatic lesions of the spinal cord yield a permanent deficit of motricity in adult mammals and specifically a loss of locomotor activity of hindlimbs when the lesion is located at the lower thoracic level. To restore this function, we have developed a paradigm of transplantation in rats based on a transection model of the spinal cord and the subsequent injection at the sublesional level of a suspension of embryonic brainstem monoaminergic neurons which play a key role in the modulation of locomotion. A genuine locomotion was characterized in transplanted animals by electromyographic and electroneurographic recordings. This correlated with a specific reinnervation pattern of targets, where typical synapses were found, and with the normalization of biochemical parameters.
Assuntos
Locomoção/fisiologia , Neurônios Motores/transplante , Paraplegia/cirurgia , Traumatismos da Medula Espinal/cirurgia , Medula Espinal , Animais , Aminas Biogênicas/fisiologia , Neurônios Motores/química , Neurônios Motores/fisiologia , Paraplegia/fisiopatologia , Paraplegia/reabilitação , Ratos , Traumatismos da Medula Espinal/fisiopatologia , Traumatismos da Medula Espinal/reabilitaçãoRESUMO
Several growth factors are candidates for the therapy of motor neurone diseases. However, there is no efficient, safe, and practicable administration route which hampers the clinical use of these potentially therapeutic agents. We show that specific and high yield gene transfer into motor neurones can be obtained by peripheral intramuscular injections of recombinant adenoviruses. These vectors are retrogradely transported from muscular motor units to motor neurone cell bodies. Gene transfer can thus be specifically targeted to particular regions of the spinal cord by appropriate choice of the injected muscle. The efficiency of gene transfer is high, with 58-100% of the motor neurones afferent to the injected muscle expressing the transgene. This new therapeutic protocol allows specific targeting of motor neurones without lesioning the spinal cord, and should avoid undesirable side effects associated with systemic administration of therapeutic factors.
Assuntos
Técnicas de Transferência de Genes , Doença dos Neurônios Motores/terapia , Medula Espinal/enzimologia , Animais , Contagem de Células , Masculino , Neurônios Motores/enzimologia , Ratos , Ratos Sprague-Dawley , beta-Galactosidase/metabolismoRESUMO
Several growth factors are candidates for the therapy of motor neurone diseases. However, there is no efficient, safe, and practicable administration route which hampers the clinical use of these potentially therapeutic agents. We show that specific and high yield gene transfer into motor neurones can be obtained by peripheral intramuscular injections of recombinant adenoviruses. These vectors are retrogradely transported from muscular motor units to motor neurone cell bodies. Gene transfer can thus be specifically targeted to particular regions of the spinal cord by appropriate choice of the injected muscle. The efficiency of gene transfer is high, with 58-100% of the motor neurones afferent to the injected muscle expressing the transgene. This new therapeutic protocol allows specific targeting of motor neurones without lesioning the spinal cord, and should avoid undesirable side effects associated with systemic administration of therapeutic factors.
Assuntos
Adenoviridae/genética , Técnicas de Transferência de Genes , Terapia Genética , Vetores Genéticos , Doença dos Neurônios Motores/terapia , beta-Galactosidase/genética , Animais , Código Genético , Injeções Intramusculares , Masculino , Fatores de Crescimento Neural/genética , Ratos , Ratos Sprague-DawleyRESUMO
The synaptic connections established by grafted noradrenergic (NA) neurons into the lesioned adult rat spinal cord were analysed using immunocytochemistry at the electron microscopic level. An embryonic cell suspension of the locus coeruleus region from E-13 rat embryos was transplanted into the spinal cord following either: (1) spinal cord transection or (2), partial selective denervation by 6-hydroxy dopamine (6-OH DA). One month after grafting, the NA-neurons established, in the two models, an innervation pattern similar to that found in the intact spinal cord. In both models, the transplanted NA-immunoreactive neurons formed extensive synaptic contacts with dendrites, spines and perikarya. The proportion of axodendritic and axospinous contacts was inverse in the two models. The first model thus reproduced more closely the normal synaptic pattern prefering dendritic targets, which could correspond to a better integration of the graft. In the second model, a partially NA-denervated spinal cord, there existed a competition between residual intrinsic and grafted neuron-derived fibres, which presumably affects synaptogenesis. In conclusion, the present study illustrate the complexity of cell interations conducting to the formation of a specific circuitry. Recognition phenomenon are likely modulated by space constraints, which ultimately shape-up the geometry of synaptic contacts.
Assuntos
Transplante de Tecido Encefálico/fisiologia , Transplante de Células/fisiologia , Transplante de Tecido Fetal/fisiologia , Neurônios/transplante , Norepinefrina/fisiologia , Traumatismos da Medula Espinal/cirurgia , Vias Aferentes/fisiologia , Animais , Imuno-Histoquímica , Locus Cerúleo/citologia , Locus Cerúleo/transplante , Masculino , Oxidopamina , Ratos , Ratos Sprague-Dawley , Traumatismos da Medula Espinal/patologia , Simpatectomia Química , Sinapses/fisiologia , Sinapses/ultraestruturaRESUMO
This study examined, in the adult rat, whether the intraspinal transplantation of a cell suspension of embryonic day (ED)13 rat locus coeruleus primordia was able to normalize the lesion-induced increase of spinal alpha 1-adrenoceptors. Two experimental models of spinal denervation were studied. The first model consisted of a complete spinal cord transection (thoracic vertebrae level T8-T9) and 1 week later, the cell suspension was transplanted below the section; the second one was obtained by a selective chemical lesion of the noradrenergic (NA) system and one month later, the cell suspension was implanted at the same level as in transected rats. Five weeks after grafting, all animals were sacrificed and spinal cord tissue sections were processed for immunohistochemical detection of noradrenaline or for quantification of alpha 1-adrenoceptors binding sites densities using [3H]prazosin as a ligand. After 6-OHDA lesion, as well as caudally to the transection, a significant increase by 21% (P < 0.01) to 68% (P < 0.001) of alpha 1-adrenoceptors densities was detected. The implantation of embryonic NA neurons into the denervated spinal cord led to a reversal of the lesion-induced increase of spinal alpha 1-adrenoceptors, five weeks later. Moreover, this reversal seems to be more effective after mechanical than after chemical denervation.
Assuntos
Transplante de Tecido Encefálico/fisiologia , Transplante de Células/fisiologia , Transplante de Tecido Fetal/fisiologia , Locus Cerúleo/transplante , Norepinefrina/fisiologia , Receptores Adrenérgicos alfa 1/metabolismo , Medula Espinal/fisiologia , Animais , Autorradiografia , Imuno-Histoquímica , Masculino , Norepinefrina/metabolismo , Oxidopamina , Prazosina , Ratos , Ratos Sprague-Dawley , Medula Espinal/metabolismo , Simpatectomia QuímicaRESUMO
We have investigated in this study the influence of a moderate hypergravity (1.8 G) on the development of monoaminergic projections to the spinal cord in the rat. Pregnant dams and their offspring were submitted to hypergravity from day 11 of gestation to postnatal day 15. Some animals were sacrificed at birth, other at postnatal day 15 and other after 8 months of normal gravity. In newborn animals, a substantial delay of the development of monoaminergic projections to the spinal cord was evidenced. In 15 days and 8 months animals, the pattern of innervation appeared anarchic, with numerous dystrophic profiles, mainly of serotonergic system. Ultrastructural examination of serotonergic projections revealed a paucity of synapses, and the frequent enveloping of serotonergic boutons by thin astrocytic profiles. We conclude that rats submitted to hypergravity during the critical period of onset of monoaminergic projections to the spinal cord are affected durably in the organization and the ultrastructure of these projections. Future studies are directed to the functional analysis of hypergravity animals, and to the influence of microgravity on the same system.
Assuntos
Gravidade Alterada , Serotonina/análise , Medula Espinal/química , Medula Espinal/embriologia , Animais , Centrifugação , Feminino , Microscopia Eletrônica , Neurônios/química , Neurônios/ultraestrutura , Gravidez , Ratos , Ratos Sprague-Dawley , Medula Espinal/citologiaRESUMO
One of the challenges of restorative neuronal transplantation in the CNS of mammals is the appropriate integration of grafted cells in the host circuitry. One key parameter is the specific influence of grafted cells upon corresponding receptors. In order to test this issue on the lesioned spinal cord of adult rats, two models of spinal cord denervation were used: the first one consisted of a complete transection 1 week prior to an intraspinal transplantation of embryonic locus coeruleus (LC) primordia cell suspension; the second one was a chemical destruction of the spinal noradrenergic (NA) system 1 month prior to a similar transplantation. Five weeks after transplantation, spinal sections were processed for autoradiographic quantification of alpha 2-adrenoceptor binding sites densities. In most regions, alpha 2-adrenoceptor densities remained comparable or higher than before graft; interestingly, in lumbar dorsal horn, lumbar intermediate zone and sacral distal dorsal horn of transected-grafted rats, they returned to control level. Results are discussed in relation to the parallel study performed concerning alpha 1-adrenoceptors.
Assuntos
Agonistas alfa-Adrenérgicos/farmacologia , Norepinefrina/farmacologia , Receptores Adrenérgicos alfa 2/análise , Traumatismos da Medula Espinal/metabolismo , Medula Espinal/química , Agonistas de Receptores Adrenérgicos alfa 2 , Antagonistas Adrenérgicos alfa/farmacologia , Animais , Denervação Autônoma , Autorradiografia , Células Cultivadas/transplante , Masculino , Ratos , Ratos Sprague-Dawley , Medula Espinal/efeitos dos fármacos , Medula Espinal/cirurgia , Trítio , Ioimbina/farmacologiaRESUMO
Lipoblastic differentiation in fibrous mesotheliomas is an extremely rare occurrence. We present the histological and immunohistochemical features of a case of localized peritoneal mesothelioma with lipoblastic differentiation in an 80-year old man and discuss the differential diagnosis with liposarcoma.
Assuntos
Tecido Adiposo/patologia , Mesotelioma/patologia , Neoplasias Peritoneais/patologia , Idoso , Idoso de 80 Anos ou mais , Biomarcadores/análise , Humanos , Imuno-Histoquímica , Masculino , Mesotelioma/química , Neoplasias Peritoneais/químicaRESUMO
Modifications of gene expression may occur in hepatitis B virus (HBV)-related chronic liver diseases, possibly also involving ribosomal RNA (rRNA) genes contained in the nucleolus. Changes in the level of transcriptional activity of rRNA genes are reflected by variations in the number and/or size of the nucleoli. Therefore a quantitative analysis of the silver-stained nucleoli (AgNus) was performed in a small series of liver needle biopsies from patients with HBV+ chronic persistent hepatitis (CPH) (n = 3), HBV+ chronic active hepatitis (CAH) (n = 3) and HBV+ cirrhosis (CIR) (n = 3). In each case, 100 hepatocytes were selected. The number of the nucleoli (AgNuN), their total area (tAgNuA), the average area of each nucleolus (xAgNuA), the nuclear area (NA) and the percentage ratio of tAgNuA related to NA (rAgNuA) were determined for each hepatocyte nucleus. The pooled mean values of all the features were significantly different (p less than 0.001) among the case groups. The results point towards a remarkable increase of nucleolar activity in CAH in comparison with CPH, whereas an additional increment of this activity is associated with the progress from CAH to CIR.
Assuntos
Nucléolo Celular/fisiologia , Vírus da Hepatite B/isolamento & purificação , Hepatite Crônica/microbiologia , Cirrose Hepática/microbiologia , Transcrição Gênica/genética , Biópsia por Agulha , Doença Crônica , Hepatite Crônica/patologia , Humanos , Processamento de Imagem Assistida por Computador , Cirrose Hepática/patologia , Coloração pela PrataRESUMO
The number and the size of silver-stained intranuclear granules, which correspond to the nucleolus and nucleolar organizer regions, have been determined by means of quantitative methods in cultured primary human mesothelial cells obtained from normal, reactive and malignant mesothelium. The mean values per nucleus of the number, the total area, the average area, and the relative area of the silver-stained granules and the mean nuclear area were determined for each of the three conditions. Normal, reactive and malignant mesothelial cells differed significantly in all the features. These findings at the optical level reflect the differing rate of the nucleolar biosynthetic activity related to the different biological properties of the three cell types, and the features can be useful morphometric descriptors in the diagnostic pathology of the mesothelium.
Assuntos
Líquido Ascítico/citologia , Nucléolo Celular/ultraestrutura , Intestinos/citologia , Mesotelioma/ultraestrutura , Região Organizadora do Nucléolo/ultraestrutura , Neoplasias Peritoneais/ultraestrutura , Biomarcadores , Biomarcadores Tumorais , Células Cultivadas , Células Epiteliais , Epitélio/patologia , Epitélio/ultraestrutura , Histocitoquímica , Humanos , Processamento de Imagem Assistida por Computador/métodos , Intestinos/ultraestrutura , Masculino , Mesotelioma/diagnóstico , Mesotelioma/patologia , Neoplasias Peritoneais/diagnóstico , Neoplasias Peritoneais/patologia , Prata , Células Tumorais Cultivadas/patologia , Células Tumorais Cultivadas/ultraestruturaRESUMO
Astrocytes play an active role in the brain and spinal cord. For example, they have a function in formation and maintenance of the blood-brain barrier, ion homeostasis, neurotransmitter transport, production of extracellular matrix, and neuromodulation. Moreover, they play a role in preserving or even restoring the structural and physiological integrity after tissue injury. Currently, the function of astrocytes was studied with regard to the controversially discussed aspects of permissivity on the one-hand-side and inhibition of the other side exerted by reactive astrocytes for axonal regrowth in the adult CNS. Accordingly, knock-out mice deficient in vimentin (VIM) and/or glial fibrillary acidic protein (GFAP), the two major IF-proteins of astrocytes, were investigated. In addition, in vitro studies were carried out, on whether the absence of one or both proteins (VIM, GFAP) influences axonal regeneration. In experimental animals, a hemisection of the spinal cord was performed utilizing the above mentioned double-mutant mice. The knock-out mice were generated by gene targeting. Double-mutants were obtained by crossing single null mice. The in vitro results indicate that both VIM and GFAP were absent in astrocytic cultures obtained from double-mutant mice. On the other side, the proteins were detected in more than 85%, of cultured cells from wild types. Co-culture of mutant mice astrocytes with neurons revealed that the neuronal density was different from that obtained in culture with wild type astrocytes. On the other side, there was a marked increase in neuronal density in co-cultures utilizing both GFAP knock-out- or double-mutant mice astrocytes again as compared to co-cultures with wild type astrocytes. Moreover, the neurite length of neurons was significantly increased in experiments with neurons growing on astrocytes from GFAP-knock-out or double-mutant mice. The in vivo experiments demonstrate an increase of nestin (NES) immunoreactivity at three days in the sectioned side of the spinal cord, in the perikaryon and astroglial processes. In double-mutant mice only a slight increase in NES-immunoreactivity was found in the lesion side, albeit confined to the perikaryon of astrocytes. Below the lesion, serotonin immunostaining was dramatically reduced three days after the insult in both sides, particularly in the lesion side. The decrease was more pronounced in double-mutant than in wild type mice. On the other side, double-mutant mice had a much higher density of serotonergic fibers in the ventral horn in the lesioned side. In conclusion, the findings demonstrate that in the absence of important astrocytic proteins as VIM and GFAP, the astroglial response to injury is significantly modified underlying reduced scar formation. Attenuation of scar formation may enhance axonal sprouting of serotonergic axons below the lesion, which specifically reinnervate motoneuron pools.