Abstract

Pluripotent stem cells (PSCs) are a unique type of cells because they exhibit the characteristics of self-renewal and pluripotency. PSCs may be induced to differentiate into any cell type, even male and female germ cells, suggesting their potential as novel cell-based therapeutic treatment for infertility problems. Spermatogenesis is an intricate biological process that starts from self-renewal of spermatogonial stem cells (SSCs) and leads to differentiated haploid spermatozoa. Errors at any stage in spermatogenesis may result in male infertility. During the past decade, much progress has been made in the derivation of male germ cells from various types of progenitor stem cells. Currently, there are two main approaches for the derivation of functional germ cells from PSCs, either the induction of in vitro differentiation to produce haploid cell products, or combination of in vitro differentiation and in vivo transplantation. The production of mature and fertile spermatozoa from stem cells might provide an unlimited source of autologous gametes for treatment of male infertility. Here, we discuss the current state of the art regarding the differentiation potential of SSCs, embryonic stem cells, and induced pluripotent stem cells to produce functional male germ cells. We also discuss the possible use of livestock-derived PSCs as a novel option for animal reproduction and infertility treatment.Electronic supplementary materialThe online version of this article (doi:10.1007/s00018-015-2020-1) contains supplementary material, which is available to authorized users.

Highlights

  • GDNF Glial cell line-derived neurotrophic factor human embryonic stem cells (hESCs) Human embryonic stem cells hiESCs Human induced embryonic stem cells human induced pluripotent stem cells (hiPSCs) Human induced pluripotent stem cells

  • We have demonstrated that bovine testicular iPSCs are useful for screening the toxicity of environmental disruptors, such as phthalate esters by examining their effects on the maintenance of stemness and pluripotency, and for identifying signaling pathways that might be affected by disruptors [36, 37]

  • We found that bovine iPSCs were more resistant to androgen receptor (AR)-dependent apoptosis than testicular cells, most likely attributed to regulation of the ARp21Cip1 cascade via p53, which showed significantly enhanced expression

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Summary

Introduction

GDNF Glial cell line-derived neurotrophic factor hESCs Human embryonic stem cells hiESCs Human induced embryonic stem cells hiPSCs Human induced pluripotent stem cells. SSCs from neonatal and adult mice can develop into pluripotent stem cells (PSCs) when cultured under specific conditions in vitro [7, 8]. We review the current status of the differentiation potential of SSCs, embryonic stem cells (ESCs), and induced pluripotent stem cells (iPSCs) towards male germ cells.

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