Mammalian target of rapamycin (mTOR): a central regulator of male fertility?

被引:42
|
作者
Jesus, Tito T. [1 ,2 ,3 ]
Oliveira, Pedro F. [1 ,2 ,4 ]
Sousa, Mario [1 ,2 ,5 ]
Cheng, C. Yan [6 ]
Alves, Marco G. [1 ,2 ,3 ]
机构
[1] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Microscopy, Lab Cell Biol, Rua Jorge Viterbo Ferreira 228, P-4050313 Oporto, Portugal
[2] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Unit Multidisciplinary Res Biomed UMIB, Rua Jorge Viterbo Ferreira 228, P-4050313 Oporto, Portugal
[3] Univ Beira Interior, CICS UBI, Hlth Sci Res Ctr, Covilha, Portugal
[4] Univ Porto, i3S, Oporto, Portugal
[5] Ctr Reprod Genet Prof Alberto Barros, Oporto, Portugal
[6] Populat Council, Ctr Biomed Res, Mary M Wohlford Lab Male Contracept Res, 1230 York Ave, New York, NY 10021 USA
关键词
mTOR; Sertoli cells; spermatogenesis; male reproduction; fertility; BLOOD-TESTIS BARRIER; HUMAN SERTOLI-CELLS; MESSENGER-RNA TRANSLATION; PROTEIN-KINASE B; COMPLEX; MTORC1; P70; S6; KINASE; TUBEROUS SCLEROSIS; RETINOIC ACID; KIT-LIGAND; SPERMATOGONIAL DIFFERENTIATION;
D O I
10.1080/10409238.2017.1279120
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mammalian target of rapamycin (mTOR) is a central regulator of cellular metabolic phenotype and is involved in virtually all aspects of cellular function. It integrates not only nutrient and energy-sensing pathways but also actin cytoskeleton organization, in response to environmental cues including growth factors and cellular energy levels. These events are pivotal for spermatogenesis and determine the reproductive potential of males. Yet, the molecular mechanisms by which mTOR signaling acts in male reproductive system remain a matter of debate. Here, we review the current knowledge on physiological and molecular events mediated by mTOR in testis and testicular cells. In recent years, mTOR inhibition has been explored as a prime strategy to develop novel therapeutic approaches to treat cancer, cardiovascular disease, autoimmunity, and metabolic disorders. However, the physiological consequences of mTOR dysregulation and inhibition to male reproductive potential are still not fully understood. Compelling evidence suggests that mTOR is an arising regulator of male fertility and better understanding of this atypical protein kinase coordinated action in testis will provide insightful information concerning its biological significance in other tissues/organs. We also discuss why a new generation of mTOR inhibitors aiming to be used in clinical practice may also need to include an integrative view on the effects in male reproductive system.
引用
收藏
页码:235 / 253
页数:19
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