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1.
National Journal of Andrology ; (12): 133-137, 2016.
Artigo em Chinês | WPRIM | ID: wpr-304738

RESUMO

<p><b>OBJECTIVE</b>To culture rat prostate glandular epithelial cells and study their barrier functions in vitro.</p><p><b>METHODS</b>Rat prostate glandular epithelial cells were cultured in vitro. The expression of the tight junction protein claudin-1 was determined by immunohistochemistry, the structure and composition of the epithelial cells observed under the inverted microscope and transmission electron microscope. The transepithelial electrical resistances (TEERs) were monitored with the Millicell system. The permeability of the prostate glandular epithelial cells was assessed by the phenol red leakage test.</p><p><b>RESULTS</b>Compact monolayer cell structures were formed in the prostate glandular epithelial cells cultured in vitro. Immunohistochemistry showed the expression of the tight junction protein claudin-1 and transmission electron microscopy confirmed the formation of tight junctions between the adjacent glandular epithelial cells. The TEERs in the cultured prostate glandular epithelial cells reached the peak of about (201.3 ± 3.5) Ω/cm2 on the 8th day. The phenol red leakage test manifested a decreased permeability of the cell layers with the increase of TEERs.</p><p><b>CONCLUSION</b>The structure and function of rat prostate glandular epithelial cells are similar to those of brain capillary endothelial cells, retinal capillary endothelial cells, and intestinal epithelial cells. In vitro cultured prostate glandular epithelial cells have the barrier function and can be used as a model for the study of blood prostate barrier in vitro.</p>


Assuntos
Animais , Masculino , Ratos , Permeabilidade da Membrana Celular , Células Cultivadas , Claudina-1 , Metabolismo , Impedância Elétrica , Células Epiteliais , Patologia , Fisiologia , Técnicas In Vitro , Microscopia Eletrônica de Transmissão , Fenolsulfonaftaleína , Farmacocinética , Próstata , Metabolismo , Patologia , Junções Íntimas
2.
National Journal of Andrology ; (12): 294-299, 2015.
Artigo em Chinês | WPRIM | ID: wpr-319505

RESUMO

<p><b>OBJECTIVE</b>To investigate the inhibitory effect of bone marrow mesenchymal stem cells (BMSCs) on E coliinduced prostatitis in rats.</p><p><b>METHODS</b>BMSCs were isolated, cultured and amplified by the attached choice method. Fifty SD rats were randomized into five groups of equal number: normal control, acute bacterial prostatitis (ABP) , chronic bacterial prostatitis (CBP), ABP + BMSCs, and CBP + BMSCs, and the animals in the latter four groups were injected with E. coli into both sides of the prostate under ultrasound guidance for 1 - 14 days to induce ABP and for 4 - 12 weeks to induce CBP. The control rats were injected with the same amount of PBS. Two weeks after injection of BMSCs into the prostates, pathomorphological changes in the prostate were observed under the light microscope and the mRNA and protein levels of IL-1β and TNF-α determined by RT-PCR and ELISA, respectively, followed by statistical analysis with SPSS 18.0.</p><p><b>RESULTS</b>Histopathological evaluation showed typical pathological inflammatory changes in the prostates of the rats in the ABP and CBP groups, including glandular structural changes, interstitial edema, inflammatory cell infiltration, and fibrous hyperplasia, which were all remarkably relieved after treated with BMSCs. The mRNA and protein levels of IL-β ([0.829 ± 0.121] and [271.75 ± 90.59] pg/ml) and TNF-α ([0.913 ± 0. 094] and [105.78 ± 19. 05] pg/ml) in the ABP and those of IL-1β ([0. 975 ± 0. 114] and [265. 31 ± 71. 34] pg/ml) and TNF-α ([0. 886 ± 0. 084] and [107. 45 ± 26. 11 ] pg/ml) in the CBP groups were significantly higher than those in the control rats ([0. 342 ± 0.087] and [45.76 17. 99] pg/ml, P <0. 05); ([0.247 ± 0.054] and ([19.42 ± 7. 75] pg/ml, P <0. 01) as well as than those in the ABP + BMSCs ([0. 433 ± 0. 072] and [51. 34 ± 22. 13] pg/ml, P < 0. 05 ) ; ( [0. 313 ± 0. 076] and [28. 38 ± 8. 78] pg/ml, P < 0. 01) and the CBP + BMSCs group ([0.396 ± 0.064] and [56.37 ± 21.22] pg/ml, P <0.05); ([0.417 ± 0.068] and [29.21 ± 10.22] pg/ml, P <0.01).</p><p><b>CONCLUSION</b>Injection of BMSCs can reduce E coli-induced prostatic inflammation reaction, which.may be associated with its reduction of inflammatory cell infiltration and the expressions of IL-1β and TNF-α in the prostate tissue.</p>


Assuntos
Animais , Humanos , Masculino , Ratos , Doença Aguda , Células da Medula Óssea , Fisiologia , Doença Crônica , Infecções por Escherichia coli , Terapêutica , Interleucina-1beta , Genética , Células-Tronco Mesenquimais , Fisiologia , Próstata , Metabolismo , Prostatite , Metabolismo , Microbiologia , Terapêutica , RNA Mensageiro , Distribuição Aleatória , Ratos Sprague-Dawley , Fator de Necrose Tumoral alfa , Genética , Metabolismo
3.
National Journal of Andrology ; (12): 460-463, 2014.
Artigo em Chinês | WPRIM | ID: wpr-309688

RESUMO

Stem cells are characterized by self-renewing, multipotent differentiation, and high proliferation and receiving more and more attention for their roles in the development and management of various diseases. There are epithelial stem cells and mesenchymal stem cells in the prostate. The markers of the epithelial stem cells include cytokeratin, stem cell antigen-1, and integrins alpha2beta1, CD49f, CD133, CD117, and CD44. The markers of the mesenchymal stem cells include CD30, CD44, CD133, neuron-specific enolase, and vascular endothelial growth factor receptor-1. Prostate stem cells are involved in the development and treatment of prostatic diseases. This review focuses on the latest progress in the studies of prostate stem cells.


Assuntos
Humanos , Masculino , Antígenos CD , Biomarcadores , Diferenciação Celular , Integrina alfa2beta1 , Próstata , Biologia Celular , Células-Tronco , Química , Biologia Celular , Fator A de Crescimento do Endotélio Vascular
4.
Chinese Journal of Traumatology ; (6): 311-314, 2008.
Artigo em Inglês | WPRIM | ID: wpr-239828

RESUMO

Massive hemorrhage from infected anastomosed site between the graft artery and the external iliac artery is one of the most serious complications of renal transplantation. Clinically, it is a rare but fatal occasion. We reported here one case of hemorrhage with infection in the iliac artery anastomosed site treated successfully with hypogastric artery autograft interposition in March 2003.


Assuntos
Adulto , Humanos , Masculino , Anastomose Cirúrgica , Artérias , Transplante , Infecções Bacterianas , Hemorragia , Cirurgia Geral , Artéria Ilíaca , Cirurgia Geral , Transplante de Rim , Complicações Pós-Operatórias , Veias Renais , Cirurgia Geral , Transplante Autólogo
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