The Expression of TLR2 and TLR3 in Sertoli Cells of Azoospermic Patients

被引:13
作者
Lakpour, Mohammad Reza [1 ,2 ]
Koruji, Morteza [3 ]
Shahverdi, Abdolhossein [4 ]
Aghajanpour, Samaneh [5 ]
Naghandar, Majid Rajabian [2 ]
Gilani, Mohammad Ali Sadighi [1 ,6 ]
Sabbaghian, Marjan [1 ]
Aflatoonian, Reza [5 ]
机构
[1] Royan Inst Reprod Biomed, ACECR, Reprod Biomed Res Ctr, Dept Androl, POB 16635-148, Tehran, Iran
[2] Payam Noor Univ, Dept Biol, Tehran, Iran
[3] Iran Univ Med Sci, Cellular & Mol Res Ctr, Dept Anat Sci, Tehran, Iran
[4] Royan Inst Reprod Biomed, ACECR, Reprod Biomed Res Ctr, Dept Embryol, Tehran, Iran
[5] Royan Inst Reprod Biomed, ACECR, Reprod Biomed Res Ctr, Dept Endocrinol & Female Infertil, Tehran, Iran
[6] Univ Tehran Med Sci, Shariati Hosp, Dept Urol, Tehran, Iran
关键词
Sertoli Cells; Testis; Fibroblast Cells; TLRs; TOLL-LIKE RECEPTORS; ANTI-MULLERIAN HORMONE; NONOBSTRUCTIVE AZOOSPERMIA; SPERMATOGENIC CELLS; REPRODUCTIVE-TRACT; IMMUNE-RESPONSES; INNATE IMMUNITY; RAT TESTES; RECOGNITION; MOUSE;
D O I
10.22074/cellj.2017.4300
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Toll-like receptors (TLRs) on Sertoli cells are thought to have essential roles in sperm protection. This study was conducted to investigate the expression of TLR2 and TLR3 in Sertoli cells of men with azoospermia. Materials and Methods: In this experimental study, testicular biopsies were taken from ten azoospermic men. Following enzymatic dissociation, the samples were moved to lectin coated petri dishes. After a few passages, all cells were cultivated and Seroli cells were sorted by flow cytometry. To confirm Sertoli cell purification, alkaline phosphatase activity (ALP) and immunohistochemistry assays were employed. The expression of TLR2 and TLR3 at the transcript and protein levels was examined with real-time quantitative reverse transcription-polymerase chain reaction (RT-QPCR) and western blot, respectively. Results: Isolation, purification and cultivation of human Sertoli cells were performed successfully. Efficacy of purification of Sertoli cells by fluorescence-activated cell sorting (FACS) sorter was similar to 97%. The type of cultured cells was confirmed by vimentin and follicle-stimulating hormone (FSH) receptor markers. Furthermore, the existence of anti-Mullerian hormone in culture was confirmed. RT-PCR showed that both genes were expressed in Sertoli cells. Consistently, proteins of both were also expressed in Sertoli cells. Moreover, QPCR showed that the relative expression of TLR3 transcripts was significantly higher than TLR2 in Sertoli cells. Although both genes are expressed in fibroblast cells, their level of expression was significantly lower than in Sertoli cells. Conclusion: This study confirmed expression of TLR2 and TLR3 in human Sertoli cells. This may be an indicator of their roles in developing immunity against pathogens as well as allo-and auto-antigens or viral antigens in seminiferous tubules.
引用
收藏
页码:375 / 385
页数:11
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