RESUMO
BACKGROUND: The beta chain of the interleukin 2/15 receptor (IL-2/15Rbeta) is induced by the expression of the EWS-WT1. A case of desmoplastic small round cell tumour (DSRCT) expressing only an unusual EWS-WT1 treated by us is reported here. AIM: To characterise an unusual form of EWS-WT1. METHODS: Frozen tissue sections of the axillary tumour were examined using a laser-assisted microdissection technique and reverse transcriptase polymerase chain reaction. RESULTS: The novel fusion of exon 8 of EWS and the defective exon 10 of WT1 (-KTS) was detected. Although it was an unusual form, the coexpression of the present EWS-WT1, IL-2/15Rbeta and Janus kinase (JAK1) mRNA was detected in the tumour cells. IL-2 and signal transducers and activators of transcription (STAT5) mRNA were detected in both tumour and stromal cells. CONCLUSION: The induction of the IL-2/15 receptor signalling pathway may contribute to tumorigenesis in DSRCT through a paracrine or an autocrine system, even though the EWS-WT1 was an unusual form.
Assuntos
Carcinoma de Células Pequenas/metabolismo , Subunidade beta de Receptor de Interleucina-2/biossíntese , Neoplasias Pulmonares/metabolismo , Proteínas de Fusão Oncogênica/metabolismo , Adulto , Sequência de Bases , Evolução Fatal , Humanos , Subunidade beta de Receptor de Interleucina-2/genética , Masculino , Dados de Sequência Molecular , Proteínas de Neoplasias/metabolismo , RNA Mensageiro/genética , RNA Neoplásico/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodosRESUMO
The effects of temperature on skin papillomas of newts (Cynops pyrrhogaster) were studied. Newts bearing these tumors were maintained for 30 weeks at 4 +/- 1 (S.E.), 10 +/- 1, 13 +/- 2, 25 +/- 1, and 30 +/- 1 degree. The diameters of the papillomas were measured externally. They decreased at 4, 25, and 30 degrees, and increased at 10 and 13 degrees. The effect of temperature on the tumor growth or regression began to appear from around the 10th week. Furthermore, when the temperatures were changed, it was possible to reverse the growth or regression of the tumors. Histologically, cell layers of the tumors became thin at 4, 25, and 30 degrees, but there were some differences between 4 and 25 or 30 degrees. The pigment layers became thick, and epidermal cells invaded dermal layer at 4 degrees, and clumps of cells separated from the surface of the tumors at 25 and 30 degrees. Mitotic indices were lower at 4, 25, and 30 degrees than in normal epidermis, but were about 3 times as high as normal tissue at 10 or 13 degrees. The relation between these results in the laboratory and seasonal fluctuations of these tumors in nature is discussed.
Assuntos
Papiloma/veterinária , Salamandridae , Neoplasias Cutâneas/veterinária , Temperatura , Animais , Índice Mitótico , Papiloma/patologia , Estações do Ano , Neoplasias Cutâneas/patologiaRESUMO
The occurrence of spontaneous skin papillomas in Japanese newts (Cynops pyrrhogaster) from Niigata prefecture in Northern Japan was monitored over four seasons covering a period of 2 years. Of 13,613 newts, 249 were found to possess papillomas. The percentage of newts with papillomas was highest in autumn, ranging from 1.93 to 5.45% of the total average. These values were more than four times as high as values obtained in the other three seasons (0.16 to 0.50%). A total of 12,167 newts were collected from their natural environment in 10 prefectures of Japan in the autumn of 1980 and 1981. Newts collected from the northern, seaside prefectures had higher papilloma rates (1.00 to 5.45%) than did newts from the Southern, Pacific Ocean prefectures of Japan (0 to 0.27%). Male and female newts were affected equally often by the epitheliomas. Virus-like bodies, resembling herpes-type virus, were found in the cytoplasm of the epitheliomas. These virus-like bodies were not seen in the control epithelium of newts with normal skin and without papilloma or in nonaffected regions of newts with papilloma. It is suggested that tumor and virus are causally related.
Assuntos
Papiloma/veterinária , Salamandridae , Neoplasias Cutâneas/veterinária , Animais , Feminino , Corpos de Inclusão Viral/ultraestrutura , Japão , Lisossomos/ultraestrutura , Masculino , Papiloma/epidemiologia , Papiloma/ultraestrutura , Estações do Ano , Neoplasias Cutâneas/epidemiologia , Neoplasias Cutâneas/ultraestruturaRESUMO
Rat and human steroid sulfatases were purified from liver and placenta, respectively, by the same procedure. The rat and human enzymes were solubilized with Triton X-100, and purified by immunoaffinity chromatography with a monoclonal antibody showing high binding activities to both the enzymes. They were further purified by high-pressure anion-exchange chromatography to compare their structural and catalytic properties. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that both enzymes had a molecular weight of 62,000. The enzymes had similar amino acid compositions and amino-terminal amino acid sequences. Significant differences of the optimum pH, Michaelis constant and maximum velocity were observed between these enzymes. The optimum pH of each enzyme varied from 6.0 to 8.0, depending on substrates and with or without Triton X-100. In detergent-free media, steroid sulfates competitively inhibited the ability of these enzymes to hydrolyze 4-nitrophenyl sulfate. In media containing Triton X-100, on the other hand, the inhibition types of the steroid sulfates on the hydrolyzing activities of the rat and human enzymes were noncompetitive- and mixed-types, respectively.
Assuntos
Microssomos Hepáticos/enzimologia , Microssomos/enzimologia , Placenta/enzimologia , Sulfatases/metabolismo , Sequência de Aminoácidos , Aminoácidos/análise , Animais , Anticorpos Monoclonais , Complexo Antígeno-Anticorpo , Cromatografia de Afinidade , Feminino , Humanos , Cinética , Substâncias Macromoleculares , Dados de Sequência Molecular , Peso Molecular , Gravidez , Ratos , Especificidade da Espécie , Especificidade por Substrato , Sulfatases/isolamento & purificaçãoRESUMO
A mouse monoclonal antibody 12B1 was raised against Golgi fractions from Sf21 insect cells and selected as Golgi-specific by immunostaining of the cells. The antigen was purified from the cells by immunoaffinity chromatography with the monoclonal antibody, and its N-terminal and internal amino acid sequences were determined. Based on the partial amino acid sequences, cDNA encoding the antigen protein was cloned and sequenced. The amino acid sequence deduced from the cDNA nucleotide sequence showed a homology to those of CALNUC family proteins, CALNUC (or nucleobindin, a calcium-binding Golgi protein with DNA-binding activity) and protein NEFA (a cell surface protein with DNA-binding, EF-hand, and acidic domains). The insect protein had two EF-hand loops at the same sites as the mammalian CALNUC family proteins, but had no leucine zipper which the mammalian homologues commonly have. An electron microscopic immunoperoxidase study demonstrated that the insect protein was localized in the cis-Golgi cisternae and cis-Golgi networks. Since this localization is identical to that of mammalian CALNUC, the insect protein was considered to be a homologue of CALNUC rather than that of NEFA. Assays involving proteinase K digestion, sodium carbonate extraction and Triton X-114 extraction revealed that the insect CALNUC-like protein was a soluble protein tightly associated with the luminal surface of Golgi membranes as reported for mammalian CALNUC. The insect protein was also shown to have calcium-binding activity as does mammalian CALNUC. These data verify that the insect protein is CALNUC. The existence of CALNUC in insect cells suggests that CALNUC is an essential calcium-binding Golgi protein in a wide range of the animal kingdom. A phylogenetic tree analysis, however, suggested that NEFA was derived from CALNUC long after the segregation of a mammalian ancestor from an insect ancestor.
Assuntos
Proteínas de Ligação a DNA/biossíntese , Complexo de Golgi/metabolismo , Substâncias de Crescimento/biossíntese , Acetilglucosaminidase/metabolismo , Sequência de Aminoácidos , Animais , Anticorpos Monoclonais/metabolismo , Western Blotting , Cálcio/metabolismo , Proteínas de Ligação ao Cálcio , Linhagem Celular , Centrifugação com Gradiente de Concentração , DNA Complementar/metabolismo , Feminino , Imunofluorescência , Imunoglobulina G/metabolismo , Imuno-Histoquímica , Insetos , Manosidases/metabolismo , Camundongos , Camundongos Endogâmicos BALB C , Microscopia Eletrônica , Dados de Sequência Molecular , Proteínas do Tecido Nervoso , Nucleobindinas , Filogenia , Ligação Proteica , Homologia de Sequência de Aminoácidos , alfa-ManosidaseRESUMO
We have produced a new protein-specific monoclonal antibody (MAb) to rat liver beta 1-->4 galactosyltransferase. This MAb, GTL2, was selected as the most reactive IgG to a periodate-treated antigen. Antigen and protein specificities of GTL2 were verified by immunoblotting of a non-glycosylated recombinant protein of human galactosyltransferase and enzymatically deglycosylated rat galactosyltransferase. Using GTL2, an immunohistochemical study was done in rat liver, epididymis, and salivary glands. Intense staining was observed in Golgi areas of epididymal duct epithelial cells, and submandibular and sublingual acinar cells. Hepatocytes showed weaker staining. Immunoelectron microscopic observation revealed that the staining was exclusively localized in trans-Golgi membranes of these cells.
Assuntos
Anticorpos Monoclonais/biossíntese , Especificidade de Anticorpos/imunologia , Microssomos Hepáticos/enzimologia , N-Acetil-Lactosamina Sintase/metabolismo , Animais , Anticorpos Monoclonais/imunologia , Eletroforese em Gel de Poliacrilamida , Epididimo/enzimologia , Complexo de Golgi/enzimologia , Immunoblotting , Técnicas Imunoenzimáticas , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Microscopia Imunoeletrônica , N-Acetil-Lactosamina Sintase/imunologia , N-Acetil-Lactosamina Sintase/isolamento & purificação , Ratos , Ratos Wistar , Glândulas Salivares/enzimologiaRESUMO
Pokeweed mitogen (PWM) lectin, known to bind branched poly-N-acetyllactosamines, has a highly selective affinity for human colorectal carcinomas. We performed light microscopic (LM) histochemistry with PWM lectin on paraffin sections of human colorectal tissues. In histological sections, normal mucosae and adenomas with mild dysplasia exhibited negative reaction (0/10, 0/13, respectively) with or without neuraminidase pre-digestion, whereas adenomas with moderate dysplasia showed a small increase in PWM lectin reactivity after neuraminidase digestion (4/23). In contrast, we observed a high incidence of positive reactivity in colorectal carcinoma without neuraminidase pre-digestion (38/44). After digestion with neuraminidase, there was increased reactivity of colorectal carcinomas in situ (7/12) and invasive carcinomas (13/32). These results imply that human colorectal carcinomas consistently contain substantial amounts of PWM-reactive branched poly-N-acetyllactosamine glycoconjugates structures. We also compared the staining patterns of PWM lectin and monoclonal antibodies (MAb) directed to Lewis X (LeX) or Lewis Y (LeY) antigen. PWM lectin reactivity was largely confined to the apical membranes of carcinoma tissues. MAb-LeX or MAb-LeY immunoreactivity was seen on the apical membranes and in the cytoplasm of both adenomas and carcinomas. Therefore, histochemical studies with this lectin should be useful for identification of carcinoma tissues and analysis of glycoconjugates associated with colorectal carcinoma.
Assuntos
Adenoma/química , Carcinoma in Situ/química , Neoplasias Colorretais/química , Glicoconjugados/análise , Adenoma/metabolismo , Adenoma/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Monoclonais/imunologia , Carcinoma in Situ/metabolismo , Carcinoma in Situ/patologia , Neoplasias Colorretais/metabolismo , Neoplasias Colorretais/patologia , Feminino , Glicoconjugados/metabolismo , Histocitoquímica , Humanos , Imuno-Histoquímica/métodos , Mucosa Intestinal/química , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Antígenos CD15/análise , Masculino , Pessoa de Meia-Idade , Mitógenos de Phytolacca americana/metabolismoRESUMO
We purified arylsulfatase C from rat liver microsomes and prepared a monoclonal antibody (P42C2) to the purified enzyme. By SDS-PAGE and immunoblotting analysis using P42C2, the molecular weight of the purified enzyme and of the enzyme in liver and kidney microsomes were estimated at 62,000 daltons. P42C2 caused little inhibition of arylsulfatase C activity, and was bound only slightly to liver microsomes. Localization of arylsulfatase C was studied at the light and electron microscopic level by the indirect immunoperoxidase method using P42C2. In rat liver, arylsulfatase C was detected mainly in the hepatocytes, and less frequently in endothelial cells, Kupffer's cells, and Ito's cells. In rat kidney, strong staining was observed in the straight portions of the proximal tubules. The podocytes, interstitial cells, endothelial cells, and epithelial cells of Henle's thin limbs were stained faintly. By electron microscopy, arylsulfatase C was found localized on the membranes of the endoplasmic reticulum and nuclear envelopes in these cells. These immunohistochemical findings agree with the localization demonstrated by an enzyme-histochemical method which we had previously developed.
Assuntos
Anticorpos Monoclonais/imunologia , Arilsulfatases/imunologia , Fígado/imunologia , Sulfatases/imunologia , Animais , Anticorpos Monoclonais/análise , Anticorpos Monoclonais/metabolismo , Arilsulfatases/análise , Arilsulfatases/metabolismo , Imuno-Histoquímica/métodos , Rim/análise , Rim/enzimologia , Rim/imunologia , Fígado/análise , Fígado/enzimologia , Masculino , Ratos , Ratos Endogâmicos , Esteril-SulfataseRESUMO
We investigated the localization of polysialic acid (PSA), neural cell adhesion molecule (NCAM), and vesicular acetylcholine transporter (VAChT) in adult rat retina by using immunofluorescence with a confocal laser scanning microscope. Western blot analysis showed a typical broad smear of PSA and isoforms of NCAM (120, 140, and 180 kD). PSA immunofluorescence revealed multistratification in the inner plexiform layer (IPL). Dual immunostaining for PSA and NCAM exhibited the selective co-expression of PSA and NCAM on Müller cells. Moreover, dual immunolabeling for PSA and VAChT completely separated the five strata in the IPL. Strata 1, 3, and 5 were immunoreactive for PSA and Strata 2 and 4 for VAChT. These results suggest the possibility that PSA molecules on Müller cells are spatially related to ON and OFF retinal channels in the IPL.
Assuntos
Proteínas de Transporte/metabolismo , Proteínas de Membrana Transportadoras , Neurônios/metabolismo , Retina/metabolismo , Ácidos Siálicos/biossíntese , Proteínas de Transporte Vesicular , Animais , Western Blotting , Técnica Indireta de Fluorescência para Anticorpo , Masculino , Microscopia Confocal , Microscopia Imunoeletrônica , Moléculas de Adesão de Célula Nervosa/metabolismo , Ratos , Ratos Wistar , Vesículas Sinápticas/metabolismo , Proteínas Vesiculares de Transporte de AcetilcolinaRESUMO
BACKGROUND: Polaprezinc has been shown to exert an anti-oxidant property in a tube experiment, protect gastric mucosa from experimental ulcerations in vivo, and accelerate the healing of gastric ulcer in humans. AIM: To examine a possible protective effect of polaprezinc on oxidant-mediated injury in primary monolayer cultures of rat gastric fundic mucosa. METHODS: Cytotoxicity was quantified by measuring 51Cr release. Whether or not polaprezinc exerts an antioxidant property was investigated by determining the effect of this agent on hydrogen peroxide (H2O2)-induced injury. The effects of polaprezinc on superoxide (O2-. ) generation as well as on ethanol (EtOH)-induced injury were also examined. Generation of O2-. was assessed by the reduction in cytochrome c. RESULTS: H2O2 caused a time- and dose-dependent increase in 51Cr release. The dose-response curve of 51Cr release by H2O2 shifted to the right in the presence of polaprezinc. Polaprezinc, at submillimolar concentrations, prevented H2O2-induced 51Cr release. EtOH also caused a dose-dependent increase in 51Cr release, which was prevented by the addition of polaprezinc. The incubation of cells with EtOH caused an increase in cytochrome c reduction, as the concentrations of EtOH increased. Polaprezinc inhibited EtOH-induced cytochrome c reduction. Protection by polaprezinc was microscopically associated with the prevention of monolayer disruption. CONCLUSIONS: Polaprezinc is antioxidative and directly protects gastric mucosal cells from noxious agents through its antioxidant properties in vitro. This finding may provide the theoretical basis for the usage of an antiulcer drug with antioxidant properties for the treatment of gastric inflammation, such as that induced by ethanol.
Assuntos
Antiulcerosos/farmacologia , Antioxidantes/farmacologia , Carnosina/análogos & derivados , Mucosa Gástrica/efeitos dos fármacos , Compostos Organometálicos/farmacologia , Animais , Carnosina/farmacologia , Células Cultivadas , Grupo dos Citocromos c/metabolismo , Etanol/toxicidade , Feminino , Peróxido de Hidrogênio/toxicidade , Masculino , Microscopia de Contraste de Fase , Ratos , Ratos Sprague-Dawley , Compostos de Zinco , Sulfato de Zinco/farmacologiaRESUMO
beta 1----4 Galactosyltransferase was purified from rat liver microsomes. Catalytic properties of the enzyme resembled those of previously purified soluble and membrane-bound beta 1----4 galactosyltransferases. The enzyme purified in the present study showed a major band around a molecular weight of 53,000 on SDS-PAGE. The NH2-terminal sequence of the enzyme was determined up to the 20th residue. The sequence was identical to the amino acid sequence from Ala-13 to Lys-32 deduced from mouse beta 1----4 galactosyltransferase cDNA. These results suggest that most of the mature enzyme in rat liver microsomes is produced by removal of the NH2-terminal 12 amino acids from a precursor polypeptide.
Assuntos
Galactosiltransferases/isolamento & purificação , Microssomos Hepáticos/enzimologia , Sequência de Aminoácidos , Animais , Precursores Enzimáticos/genética , Galactosiltransferases/genética , Galactosiltransferases/metabolismo , Concentração de Íons de Hidrogênio , Técnicas In Vitro , Dados de Sequência Molecular , Peso Molecular , Ratos , Ratos Endogâmicos , Homologia de Sequência do Ácido NucleicoRESUMO
To clarify the involvement of peroxisome proliferator-activated receptors (PPARs) in atherosclerotic plaque formation, we investigated the expression patterns of mRNA and protein of PPARalpha and PPARgamma in human aorta. Atheromatous plaque, fatty streak, and diffuse intimal thickening (DIT) were separated macroscopically, and each sample was divided into halves. Half of them were used for analysis of mRNA expression with reverse transcription-polymerase chain reaction and the others were used for histologic analysis. Both PPARalpha and PPARgamma mRNA were detected in all atheromatous plaques, all fatty streaks, and in some DIT. However, expressions of PPARalpha and PPARgamma were obviously less frequently found in DIT than in atheromatous plaques, and the intensity of these expressions was stronger in the atheromatous plaques than in the DIT. Compared with PPARalpha, PPARgamma mRNA was expressed more frequently in atheromatous plaques. In atheromatous plaques, PPARgamma mRNA was expressed independently, whereas PPARalpha mRNA was coexpressed with PPARgamma. PPARgamma protein was obviously found in the nuclei of endothelial cells, macrophages, mononuclear cells, and smooth muscle cells in the aortic intima. These results suggest that expressions of PPARalpha and PPARgamma in human aortic wall are involved in atherogenesis from the early stages.
Assuntos
Arteriosclerose/fisiopatologia , Receptores Citoplasmáticos e Nucleares/classificação , Fatores de Transcrição/classificação , Arteriosclerose/patologia , Humanos , Reação em Cadeia da Polimerase , Isoformas de Proteínas/análise , Isoformas de Proteínas/classificação , Isoformas de Proteínas/genética , Receptores Citoplasmáticos e Nucleares/análise , Receptores Citoplasmáticos e Nucleares/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fatores de Transcrição/análise , Fatores de Transcrição/genéticaRESUMO
We investigated the influence of glycated low density lipoprotein (LDL) for vascular smooth muscle cell (SMC) proliferation or injury. We utilized glycated, slightly oxidized LDL (GLDL-LOX), glycated, auto-oxidized LDL (GLDL) and glycated, metal-induced extensively oxidized LDL (GLDL-OX) to examine the effect of glycation itself or combined glycation and oxidation on SMC. GLDL-LOX induced SMC proliferation and migration, and increased the number of platelet-derived growth factor receptor, beta subunits, (PDGF-R) positive SMC. Also, GLDL-LOX promoted protease activity, compared with the other groups including native LDL (control). GLDL and GLDL-OX demonstrated SMC injury with apoptosis and Bax protein expression, compared with native LDL and GLDL-LOX. These results suggested that LDL glycation contributed to the progression of atherosclerosis by promoting SMC migration and proliferation, with little dependence on oxidative modification. Secondary auto-oxidation adding to glycation induced SMC apoptosis, and SMC injury occurred in the state of strong oxidation with glycation. We concluded that LDL glycation might play a key role in the progression of atherosclerosis in diabetes, and glycated LDL promoted atherosclerosis, even with little assistance from oxidation.
Assuntos
Lipoproteínas LDL/farmacologia , Músculo Liso Vascular/citologia , Músculo Liso Vascular/efeitos dos fármacos , Proteínas Proto-Oncogênicas c-bcl-2 , Apoptose/efeitos dos fármacos , Arteriosclerose/etiologia , Divisão Celular/efeitos dos fármacos , Movimento Celular/efeitos dos fármacos , Células Cultivadas , Angiopatias Diabéticas/etiologia , Endopeptidases/metabolismo , Glicosilação , Humanos , Imuno-Histoquímica , Lipoproteínas LDL/química , Músculo Liso Vascular/lesões , Oxirredução , Proteínas Proto-Oncogênicas/metabolismo , Receptores do Fator de Crescimento Derivado de Plaquetas/metabolismo , Proteína X Associada a bcl-2RESUMO
We have investigated the effects of copper-zinc type superoxide dismutase (Cu, Zn-SOD) on the function of oxidized low density lipoprotein, utilizing cultured smooth muscle cells (SMC), obtained from rabbit aorta. We added native LDL (nLDL), minimally oxidized LDL (MmLDL) and copper ion-induced oxidized LDL (OxLDL) to the culture media. No remarkable change was found out by adding nLDL. The numbers of SMC, including migrated SMC, were increased by the addition of MmLDL. Cu, Zn-SOD significantly inhibited the reactions induced by MmLDL. The SMC numbers were markedly decreased by OxLDL addition without recovery by adding Cu, Zn-SOD. Thus, MmLDL significantly promoted the SMC proliferation and migration. OxLDL revealed strong cytotoxicity against SMC. Cu, Zn-SOD inhibited both the migration and the proliferation of SMC induced by MmLDL, and did not alter the effect of OxLDL. In conclusion, Cu, Zn-SOD inhibited some functions of MmLDL, and may play an important role in protecting against the atherosclerotic processes evoked by MmLDL.
Assuntos
Movimento Celular/efeitos dos fármacos , Lipoproteínas LDL/fisiologia , Músculo Liso Vascular/efeitos dos fármacos , Superóxido Dismutase/farmacologia , Animais , Divisão Celular/efeitos dos fármacos , Células Cultivadas , Masculino , Músculo Liso Vascular/citologia , Oxirredução , CoelhosRESUMO
A silver colloid staining technique for identifying nucleolar organizer region-associated proteins (Ag-NORs) was applied to 17 primary gliomas and 16 meningiomas. These comprised 8 glioblastomas, one pleomorphic xanthoastrocytoma, 8 benign astrocytoma, 10 nonrecurrent meningiomas and 6 recurrent meningiomas, in which the mean number of Ag-NORs' per nuclei, were 3.37, 2.34, 2.57, 2.16 and 2.80 respectively, identifying significant differences among these groups. Ag-NORs of four giant cell glioblastomas showed low numbers of Ag-NORs, suggesting better prognosis. In spite of the time consuming and complicated counting method Ag-NORs is reproductive and useful as a tool for estimating the proliferating potential of various brain tumors, and appears to widely applicable in clinical laboratories.
Assuntos
Neoplasias do Sistema Nervoso Central/patologia , Glioma/patologia , Neoplasias Meníngeas/patologia , Meningioma/patologia , Proteínas Nucleares/análise , Região Organizadora do Nucléolo/química , Adolescente , Adulto , Idoso , Antígenos Nucleares , Criança , Pré-Escolar , Feminino , Histocitoquímica , Humanos , Masculino , Pessoa de Meia-Idade , Prognóstico , Prata , Coloração e RotulagemRESUMO
We studied immunohistochemically estrogen receptors (ER) in 25 meningiomas removed from 20 patients using formalin-paraffin sections. Estrogen and progesterone receptors were studies in three case of meningiomas using frozen sections, also. Only two cases show positive reactions for estrogen receptor using formalin-paraffin sections. No correlation was found between estrogen receptor state and histological type, or biological behavior except for sex. Frozen sections failed to show the positive reaction for estrogen or progesterone receptors at all. The data suggest that estrogen receptors are detected in a few of the case with meningioma. Immunohistochemical analysis for estrogen receptor do not offer the useful informations in histopathological diagnosis or estimation of biological behaviors for meningioma on routine laboratory works.
Assuntos
Neoplasias Meníngeas/química , Meningioma/química , Receptores de Estrogênio/análise , Adulto , Idoso , Feminino , Secções Congeladas , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Inclusão em Parafina , Receptores de Progesterona/análiseRESUMO
Atherosclerotic plaque with central depression (depressed lesion) was firstly proposed in our previous report as one of the morphological features of regressed lesions, which was characterized by the presence of isolated, well defined lesions with a centrally depressed area and smooth surface. They were obviously different from atherosclerotic plaques with ulceration (ulcerated plaques) in elderly autopsy cases. In this study, 30 ulcerated plaques obtained from specimens of the elderly aortas were histologically and immunohistochemically investigated to clarify the morphogenesis of the depressed lesion and its correlation to the ulcerated plaque. These depressed lesions were divided into 4 groups according to their derivation; (a) fused lesion of multiple fibrous plaques, (b) regressing lesion of plaques, (c) healed ulcerated plaques, and (d) mixed type of these lesions. Regeneration of endothelial cell was noted in the peripheral zone of ulcerated plaques, and collagen type IV was also increased in the stroma of these ulcerated plaques. These were healed ulcerated plaques. The ulcerated plaques with complete restoration of endothelial cells on the ulcerated surface may become atherosclerotic plaques with central depression. These lesions are one of the histological features of regression in advanced atherosclerosis.
Assuntos
Aorta/patologia , Doenças da Aorta/patologia , Arteriosclerose/patologia , Idoso , Endotélio Vascular/patologia , Feminino , Humanos , Masculino , Úlcera/patologiaRESUMO
Atherosclerotic plaque with central depression (depressed lesions) have been proposed as one morphological feature of atherosclerotic regression in the elderly. We have also revealed that depressed lesions have been found not only in the aorta of elderly human but also in rabbit aorta. In this study a relationship between apoptosis and atherosclerotic regression was immunohistochemically studied to clarify the possibility of the pathogenesis of depressed lesion in rabbit aorta. Twenty male New Zealand White rabbit (NZW) were fed with a 1.0% cholesterol diet during a 12-week atherogenic induction period. Then they were fed only with a basic diet for 36-week (n = 6) and 48-week (n = 6, experimental group) regression periods. A control group was fed with 1.0% cholesterol diet for 12-week (n = 2) and 60-week (n = 6). They were killed and aortas were fixed with formalin. Sections obtained from aortas were processed for histological and immunohistochemical studies including the TUNEL method, staining with Ki-67 and others. Several depressed lesions were found in the aortas of NZW animal, but none were noted in control aortas. Results of surface involvement in the experimental groups were significantly lower than in the control, and the aortas of the experimental group had atherosclerotic regression. Apoptosis was found in the depressed lesions, which had more apoptotic cells than non-regressed atherosclerotic plaques. Furthermore, the apoptotic cells were significantly greater in the center of depressed lesions than in marginal areas. Ki-67 staining was positive in the atherosclerotic plaque, but negative in the depressed lesions. It appears that the NZW aortic atherosclerotic plaques may transform to depressed lesions with apoptosis. Atherosclerotic regression has been associated with apoptosis.
Assuntos
Aorta/patologia , Apoptose , Arteriosclerose/patologia , Animais , Arteriosclerose/etiologia , Dieta Aterogênica , Masculino , CoelhosRESUMO
A total of 161 atherosclerotic plaques from 50 aortas in elderly autopsy cases were pathomorphologically investigated to clarify the pathogenesis of atherosclerotic plaque with central depression. Atherosclerotic plaques with central depression, with well defined borders were employed for this study, ulcerated plaques being excluded. Pathomorphological findings showed that plaques with central depression could be divided into four groups according to their derivation respectively; (a) fused lesion of multiple fibrous plaque, (b) regressing lesion of plaque, (c) healing lesion of ulcerated atheromatous plaque, (d) mixed type. Finally, it was suggested that atherosclerotic regression may cause some central depression in the atheromatous plaques.
Assuntos
Arteriosclerose/patologia , Idoso , Aorta/patologia , Humanos , Pessoa de Meia-IdadeRESUMO
Atherosclerotic plaque with central depression (depressed lesion) may indicate regression of atherosclerosis in the aorta. Aortic depressed lesions have a solitary elevated area of plaque with a sharply-bordered roung depression in its center and no area ulceration. This may be interpretable as a sign of regression of atherosclerosis. To clarify the pathogenesis of depressed lesion, we studied clinical risk factors such as hypercholesterolemia in patients with depressed lesions that were confirmed at autopsy. The patients were divided into 3 groups according to their total cholesterol level at autopsy: a high-risk group (> or = 220 mg/dl), a moderate-risk group (180-220 mg/dl), and a low-risk group (< or = 180 mg/dl). Depressed lesions were found in 16.4% of those in the high-risk group, in 14.6% of those in the moderate-risk group and in 69.0% of those in the low-risk group. Severe aortic atherosclerosis was found in 69.8% of the patients; 50.9% of those with severe disease were in the-low risk group. Depressed lesions were also found in those with low levels of low-density lipoprotein cholesterol (< or = 140 mg/dl), 58.8% of whom were found to have severe atherosclerosis. There was no relationship between total cholesterol level and the presence of depressed lesions. However, a clinical prevention trial may result in sufficient control of ahterosclerosis among those in the high-risk group and may also lead to regression of aortic lesions.