Sertoli cells are the target environmental toxicants in the testis - a mechanistic and therapeutic insight

被引:96
作者
Gao, Ying [1 ]
Mruk, Dolores D. [1 ]
Cheng, C. Yan [1 ]
机构
[1] Populat Council, Ctr Biomed Res, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
environmental toxicant; Sertoli cells; spermatogenesis; testis; FOCAL ADHESION KINASE; F-ACTIN ORGANIZATION; BISPHENOL-A; BARRIER DYNAMICS; SEMEN QUALITY; ECTOPLASMIC SPECIALIZATION; PROTEIN COMPLEX; REGIONAL DIFFERENCES; SPERMATID TRANSPORT; INDUCED APOPTOSIS;
D O I
10.1517/14728222.2015.1039513
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Sertoli cells support germ cell development in the testis via an elaborate network of cell junctions that confers structural, communicating, and signaling support. However, Sertoli cell junctions and cytoskeletons are the target of environmental toxicants. Because germ cells rely on Sertoli cells for the provision of structural/functional/nutritional support, exposure of males to toxicants leads to germ cell exfoliation due to Sertoli cell injuries. Interestingly, the molecular mechanism(s) by which toxicants induce cytoskeletal disruption that leads to germ cell exfoliation is unclear, until recent years, which are discussed herein. This information can possibly be used to therapeutically manage toxicant-induced infertility/subfertility in human males. Areas covered: In this review, we provide a brief update on the use of Sertoli cell system developed for rodents and humans in vitro, which can be deployed in any research laboratory with minimal upfront setup costs. These systems can be used to collect reliable data applicable to studies in vivo. We also discuss the latest findings on the mechanisms by which toxicants induce Sertoli cell injury, in particular cytoskeletal disruption. We also identify candidate molecules that are likely targets of toxicants. Expert opinion: We provide two hypothetical models delineating the mechanism by which toxicants induce germ cell exfoliation and blood-testis barrier disruption. We also discuss molecules that are the targets of toxicants as therapeutic candidates.
引用
收藏
页码:1073 / 1090
页数:18
相关论文
共 103 条
[1]   Proliferative Activity In Vitro and DNA Repair Indicate that Adult Mouse and Human Sertoli Cells Are Not Terminally Differentiated, Quiescent Cells [J].
Ahmed, Emad A. ;
Barten-van Rijbroek, Angelique D. ;
Kal, Henk B. ;
Sadri-Ardekani, Hooman ;
Mizrak, S. Canan ;
van Pelt, Ans M. M. ;
de Rooij, Dirk G. .
BIOLOGY OF REPRODUCTION, 2009, 80 (06) :1084-1091
[2]   Oxidative stress and male reproductive health [J].
Aitken, Robert J. ;
Smith, Tegan B. ;
Jobling, Matthew S. ;
Baker, Mark A. ;
De Iuliis, Geoffry N. .
ASIAN JOURNAL OF ANDROLOGY, 2014, 16 (01) :31-38
[3]  
[Anonymous], 2014, Spermatogenesis, DOI DOI 10.4161/21565562.2014.981485
[4]   Nonylphenol alters connexin 43 levels and connexin 43 phosphorylation via an inhibition of the p38-mitogen-activated protein kinase pathway [J].
Aravindakshan, J ;
Cyr, DG .
BIOLOGY OF REPRODUCTION, 2005, 72 (05) :1232-1240
[5]   A complex containing α6β1-integrin and phosphorylated focal adhesion kinase between Sertoli cells and elongated spermatids during spermatid release from the seminiferous epithelium [J].
Beardsley, Amanda ;
Robertson, David M. ;
O'Donnell, Liza .
JOURNAL OF ENDOCRINOLOGY, 2006, 190 (03) :759-770
[6]   2,5-hexanedione-induced testicular injury [J].
Boekelheide, K ;
Fleming, SL ;
Allio, T ;
Embree-Ku, ME ;
Hall, SJ ;
Johnson, KJ ;
Kwon, EJ ;
Patel, SR ;
Rasoulpour, RJ ;
Schoenfeld, HA ;
Thompson, S .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2003, 43 :125-147
[7]  
BYERS SW, 1986, J ANDROL, V7, P59
[8]  
CALALB MB, 1995, MOL CELL BIOL, V15, P954
[9]   EVIDENCE FOR DECREASING QUALITY OF SEMEN DURING PAST 50 YEARS [J].
CARLSEN, E ;
GIWERCMAN, A ;
KEIDING, N ;
SKAKKEBAEK, NE .
BRITISH MEDICAL JOURNAL, 1992, 305 (6854) :609-613
[10]   A critical review of perfluorooctanoate and perfluorooctanesulfonate exposure and cancer risk in humans [J].
Chang, Ellen T. ;
Adami, Hans-Olov ;
Boffetta, Paolo ;
Cole, Philip ;
Starr, Thomas B. ;
Mandel, Jack S. .
CRITICAL REVIEWS IN TOXICOLOGY, 2014, 44 :1-81