Low intraprostatic DHT promotes the infiltration of CD8+ T cells in BPH tissues via modulation of CCL5 secretion.
Low intraprostatic DHT promotes the infiltration of CD8+ T cells in BPH tissues via modulation of CCL5 secretion.
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低前列腺内 DHT 通过调节 CCL5 分泌促进 BPH 组织中 CD8 T 细胞的浸润
DOI:
10.1155/2014/397815
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发表时间:
2014
影响因子:
4.6
通讯作者:
Jin J
中科院分区:
文献类型:
--
作者:
Fan Y;Hu S;Liu J;Xiao F;Li X;Yu W;Cui Y;Sun M;Lv T;He Q;Jin J
Clinical studies suggested thatandrogen might be associated with infiltrating T cells in prostate of benign prostatic hyperplasia (BPH) patients, but detail of T-cell subset and mechanism still remained unclear. The present study tested the hypothesis that intraprostatic 5α-dihydrotestosterone (DHT) exerts effects on T cells recruitment by BPH epithelial cells. Prostate tissues from 64 cases of BPH patients after transurethral resection of prostate (TURP) were divided into 2 groups: (1) no medication history; (2) administration of 5α-reductase type II inhibitor-finasteride 5 mg daily for at least 6 months before surgery. Group 2 presented significantly higher CD8+ T cells infiltration than group 1, but no changes in CD4+ T cells (immunohistochemistry and flow cytometry). In vitro study more CD8+ T cell migrated to the prostate tissue lysates from group 2 and BPH-1 cells in low DHT condition. Transcription of chemokine (C-C motif) Ligand 5 (CCL5) mRNA in BPH-1 cells and chemokine (C-C motif) receptor 5 (CCR5) mRNA in CD8+ T cells were upregulated in low DHT condition (q-PCR). CCL5 expression was also identified to be higher in group 2 prostate tissues by IHC. This study suggested that intraprostatic DHT may participate in regulating inflammatory response which was induced by human prostatic epithelial cell, via modulating CCL5 secretion.
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影响因子:
4
作者:
Vignozzi, Linda;Cellai, Ilaria;Maggi, Mario
通讯作者:
Maggi, Mario
影响因子:
4
作者:
Vignozzi, Linda;Morelli, Annamaria;Maggi, Mario
通讯作者:
Maggi, Mario
影响因子:
23.4
作者:
Nickel, J. Curtis;Roehrborn, Claus G.;Rittmaster, Roger S.
通讯作者:
Rittmaster, Roger S.
影响因子:
6.6
作者:
Wei, JT;Calhoun, E;Jacobsen, SJ
通讯作者:
Jacobsen, SJ
DOI:
10.1073/pnas.89.22.10787
发表时间:
1992-11-15
影响因子:
11.1
作者:
HARRIS, G;AZZOLINA, B;ELLSWORTH, K
通讯作者:
ELLSWORTH, K