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1.
An. bras. dermatol ; 94(2): 211-213, Mar.-Apr. 2019. graf
Artigo em Inglês | LILACS | ID: biblio-1001126

RESUMO

Abstract Cutaneous collagenous vasculopathy is a rare acquired idiopathic microangiopathy characterized by progressive development of diffuse asymptomatic telangiectasias and histologically by accumulation of collagen type IV around the affected vessels. It is diagnosed by its clinical history, confirmed by light microscopy with collagen-specific immunostaining. We report a case of a patient with extensive acquired telangiectasias on the left arm, clinically resembling unilateral nevoid telangiectasia. Dilated blood vessels with thickened walls were observed in the dermis. Immunohistochemistry with collagen IV antibodies revealed marked collagen deposition around the vessels, confirming the diagnosis. Transmission electron microscopy observed duplicate and triplicate vascular basal membrane associated with deposition of amorphous material around the membranes.


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Telangiectasia/diagnóstico por imagem , Dermatopatias Vasculares/diagnóstico por imagem , Doenças do Colágeno/diagnóstico por imagem , Braço , Telangiectasia/patologia , Dermatopatias Vasculares/patologia , Doenças do Colágeno/patologia , Colágeno Tipo IV/metabolismo , Microscopia Eletrônica de Transmissão , Microscopia
2.
Acta cir. bras ; 34(1): e20190010000007, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-983684

RESUMO

Abstract Purpose: To investigate the impact of Ramipril (RAM) on the expressions of insulin-like growth factor-1 (IGF-1) and renal mesangial matrix (RMM) in rats with diabetic nephropathy (DN). Methods: The Sprague Dawley rats were divided into normal control (NC) group (n = 12), DN group (n = 11), and DN+RAM group (n = 12). The ratio of renal weight to body weight (RBT), fasting blood glucose (FBG), HbA1c, 24-h urine protein (TPU), blood urea nitrogen (BUN), creatinine (Cr), renal pathological changes, the levels of IGF-1, fibronectin (FN), type IV collagen (Col-IV), and matrix metalloproteinases (MMP)-2 were compared among the groups. Results: Compared with NC group, the RBT, FBG, HbA1c, TPU, BUN, Cr, and RMM in DN group were significantly increased (P < 0.05), the IGF-1, FN, and Col-IV were significantly upregulated (P < 0.05), while MMP was significantly downregulated (P < 0.05). Compared with DN group, the indexes except for the FBG and HbA1c in DN+RAM group were significantly improved (P < 0.05), among which IGF-1 exhibited significant positive correlation with TPU(r=0.937), FN(r=0.896) and Col-IV(r=0.871), while significant negative correlation with MMP-2 (r=-0.826) (P<0.05). Conclusion: RAM may protect the kidneys by suppressing IGF-1 and mitigating the accumulation of RMM.


Assuntos
Animais , Masculino , Ratos , Fator de Crescimento Insulin-Like I/antagonistas & inibidores , Inibidores da Enzima Conversora de Angiotensina/farmacologia , Ramipril/farmacologia , Nefropatias Diabéticas/tratamento farmacológico , Células Mesangiais/efeitos dos fármacos , Fator de Crescimento Insulin-Like I/metabolismo , Imuno-Histoquímica , Fibronectinas/efeitos dos fármacos , Fibronectinas/metabolismo , Ratos Sprague-Dawley , Metaloproteinases da Matriz/efeitos dos fármacos , Metaloproteinases da Matriz/metabolismo , Colágeno Tipo IV/efeitos adversos , Colágeno Tipo IV/metabolismo , Nefropatias Diabéticas/metabolismo , Células Mesangiais/metabolismo
3.
Braz. j. med. biol. res ; 49(2): e4118, 2016. tab, graf
Artigo em Inglês | LILACS | ID: lil-766982

RESUMO

The aim of this study was to determine the effects of intermittent passive manual stretching on various proteins involved in force transmission in skeletal muscle. Female Wistar weanling rats were randomly assigned to 5 groups: 2 control groups containing 21- and 30-day-old rats that received neither immobilization nor stretching, and 3 test groups that received 1) passive stretching over 3 days, 2) immobilization for 7 days and then passive stretching over 3 days, or 3) immobilization for 7 days. Maximal plantar flexion in the right hind limb was imposed, and the stretching protocol of 10 repetitions of 30 s stretches was applied. The soleus muscles were harvested and processed for HE and picrosirius staining; immunohistochemical analysis of collagen types I, III, IV, desmin, and vimentin; and immunofluorescence labeling of dystrophin and CD68. The numbers of desmin- and vimentin-positive cells were significantly decreased compared with those in the control following immobilization, regardless of whether stretching was applied (P<0.05). In addition, the semi-quantitative analysis showed that collagen type I was increased and type IV was decreased in the immobilized animals, regardless of whether the stretching protocol was applied. In conclusion, the largest changes in response to stretching were observed in muscles that had been previously immobilized, and the stretching protocol applied here did not mitigate the immobilization-induced muscle changes. Muscle disuse adversely affected several proteins involved in the transmission of forces between the intracellular and extracellular compartments. Thus, the 3-day rehabilitation period tested here did not provide sufficient time for the muscles to recover from the disuse maladaptations in animals undergoing postnatal development.


Assuntos
Animais , Feminino , Imobilização/fisiologia , Exercícios de Alongamento Muscular , Fibras Musculares Esqueléticas/metabolismo , Proteínas Musculares/metabolismo , Força Muscular/fisiologia , Antígenos CD/análise , Antígenos de Diferenciação Mielomonocítica/análise , Colágeno Tipo I/análise , Colágeno Tipo I/metabolismo , Colágeno Tipo III/análise , Colágeno Tipo III/metabolismo , Colágeno Tipo IV/análise , Colágeno Tipo IV/metabolismo , Desmina/análise , Desmina/metabolismo , Distrofina/análise , Imunofluorescência , Corpos de Inclusão/metabolismo , Distribuição Aleatória , Ratos Wistar , Fatores de Tempo , Vimentina/análise , Vimentina/metabolismo
4.
Braz. j. med. biol. res ; 44(7): 682-687, July 2011. ilus, tab
Artigo em Inglês | LILACS | ID: lil-595697

RESUMO

We investigated the reactivity and expression of basal lamina collagen by Schwann cells (SCs) cultivated on a supraorganized bovine-derived collagen substrate. SC cultures were obtained from sciatic nerves of neonatal Sprague-Dawley rats and seeded on 24-well culture plates containing collagen substrate. The homogeneity of the cultures was evaluated with an SC marker antibody (anti-S-100). After 1 week, the cultures were fixed and processed for immunocytochemistry by using antibodies against type IV collagen, S-100 and p75NTR (pan neurotrophin receptor) and for scanning electron microscopy (SEM). Positive labeling with antibodies to the cited molecules was observed, indicating that the collagen substrate stimulates SC alignment and adhesion (collagen IV labeling - organized collagen substrate: 706.33 ± 370.86, non-organized collagen substrate: 744.00 ± 262.09; S-100 labeling - organized collagen: 3809.00 ± 120.28, non-organized collagen: 3026.00 ± 144.63, P < 0.05) and reactivity (p75NTR labeling - organized collagen: 2156.33 ± 561.78, non-organized collagen: 1424.00 ± 405.90, P < 0.05; means ± standard error of the mean in absorbance units). Cell alignment and adhesion to the substrate were confirmed by SEM analysis. The present results indicate that the collagen substrate with an aligned suprastructure, as seen by polarized light microscopy, provides an adequate scaffold for SCs, which in turn may increase the efficiency of the nerve regenerative process after in vivo repair.


Assuntos
Animais , Bovinos , Ratos , Colágeno Tipo IV/metabolismo , Matriz Extracelular/metabolismo , Regeneração Nervosa/fisiologia , Receptores de Fator de Crescimento Neural/análise , /análise , Células de Schwann/metabolismo , Polaridade Celular , Forma Celular , Células Cultivadas , Colágeno Tipo IV/análise , Imuno-Histoquímica , Teste de Materiais , Microscopia Eletrônica de Varredura , Polímeros/química , Ratos Sprague-Dawley , Receptores de Fator de Crescimento Neural/imunologia , /imunologia , Nervo Isquiático , Coloração e Rotulagem , Células de Schwann/citologia
5.
Experimental & Molecular Medicine ; : 74-83, 2007.
Artigo em Inglês | WPRIM | ID: wpr-37553

RESUMO

Non-enzymatic nitrite induced collagen cross-linking results in changes reminiscent of age-related damage and parallels the well-known model system, non-enzymatic glycation. We have recently observed that nitrite modification of basement membrane proteins can induce deleterious effects on overlying retinal pigment epithelial cells in studies relevant to age-related macular degeneration. The present work was undertaken in order to confirm 3-nitro-tyrosine (3-NT) as a product of the reaction and to identify the site specificity of nitration in collagen IV, a major component of basement membranes. Human collagen type IV was modified via incubation with 200 mM NaNO2 (pH=7.38) for one week at 37degrees C. The modified protein was prepared in 2 different ways, including acid hydrolysis and trypsin digestion for site specificity determination. The samples were analyzed by LC/MS using a C12 RP column. Site specificity was determined from tandem MS/MS data utilizing TurboSEQUEST software and the Swiss-Prot sequence database. 3-NT was detected in protein digests and acid hydrolysates of nitrite modified collagen IV. Positive identification with standard 3-NT was confirmed by identical Rt, lambda(max)=279 nm and 355 nm, and m/z=227. Analyses of tryptic digests identified four sites of tyrosine nitration, alpha1(IV)Y348, alpha1(IV)Y534, alpha2(IV)Y327, and alpha2(IV)Y1081. These sites are located in the triple-helical region of the protein and provide clues regarding potential sites for nitrite modification in collagen type IV.


Assuntos
Humanos , Tirosina/metabolismo , Espectrometria de Massas em Tandem , Especificidade por Substrato , Nitritos/metabolismo , Colágeno Tipo IV/metabolismo , Cromatografia Líquida , Sítios de Ligação
6.
Journal of Forensic Medicine ; (6): 413-416, 2006.
Artigo em Chinês | WPRIM | ID: wpr-983236

RESUMO

OBJECTIVE@#To investigate the structural characteristics of the cerebral small vessels with an unknown type of pathological lesion (UTPL).@*METHODS@#Contents of beta-amyloid, alpha-actin and collagen IV in cerebral small vessels with UTPL were studied by Congo red staining, immunohistochemical staining and computer image analysis.@*RESULTS@#The low expression levels of alpha-actin and collagen IV (P<0.05) were observed in tunica media of the vessels with UTPL, and no positive expression of beta-amyloid (P>0.05) was observed in these vessel walls. The expressions of proteins mentioned above in UTPL were different from those of cerebral amyloid angiopathy(CAA) and hyaline arteriolosclerosis.@*CONCLUSION@#UTPL was different from CAA or hyaline arteriolosclerosis in pathologic feature.


Assuntos
Humanos , Actinas/metabolismo , Peptídeos beta-Amiloides/metabolismo , Autopsia , Vasos Sanguíneos/ultraestrutura , Encéfalo/patologia , Angiopatia Amiloide Cerebral/patologia , Colágeno Tipo IV/metabolismo , Processamento de Imagem Assistida por Computador , Imuno-Histoquímica , Coloração e Rotulagem , Hemorragia Subaracnóidea/patologia
7.
Braz. j. med. biol. res ; 36(1): 29-37, Jan. 2003. ilus
Artigo em Inglês | LILACS | ID: lil-326314

RESUMO

Nascent procollagen peptides and other secretory proteins are transported across the endoplasmic reticulum (ER) membrane through a protein-conducting channel called translocon. Sec61alpha, a multispanning membrane translocon protein, has been implicated as being essential for translocation of polypeptide chains into the cisterns of the ER. Sec61alpha forms a protein complex with collagen and Hsp47, an ER-resident heat shock protein that binds specifically to collagen. However, it is not known whether Sec61alpha is ubiquitously produced in collagen-producing F9 teratocarcinoma cells or under heat shock treatment. Furthermore, the production and utilization of Sec61alpha may depend on the stage of cell differentiation. Cultured F9 teratocarcinoma cells are capable of differentiation in response to low concentrations of retinoic acid. This differentiation results in loss of tumorigenicity. Mouse F9 cells were grown in culture medium at 37ºC and 43ºC (heat shock treatment) treated or not with retinoic acid, and labeled in certain instances with 35S-methionine. Membrane-bound polysomes of procollagen IV were then isolated. Immunoprecipitation and Western blot analysis were performed using polyclonal antibodies against collagen IV, Hsp47 and Sec61alpha. Under retinoic acid-untreated conditions, F9 cells produced undetectable amounts of Sec61alpha. Sec61alpha, Hsp47 and type IV collagen levels were increased after retinoic acid treatment. Heat shock treatment did not alter Sec61alpha levels, suggesting that Sec61alpha production is probably not affected by heat shock. These data indicate that the enhanced production of Sec61alpha in retinoic acid-induced F9 teratocarcinoma cells parallels the increased synthesis of Hsp47 and collagen type IV


Assuntos
Animais , Camundongos , Antineoplásicos , Colágeno Tipo IV/metabolismo , Proteínas de Choque Térmico , Proteínas de Membrana , Tretinoína , Células Tumorais Cultivadas , Western Blotting , Diferenciação Celular , Colágeno Tipo IV/efeitos dos fármacos , Eletroforese em Gel de Poliacrilamida , Proteínas de Choque Térmico , Medições Luminescentes , Proteínas de Membrana , Teratocarcinoma
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