2021
DOI: 10.1016/j.mce.2021.111179
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Differentiation of seminiferous tubule-associated stem cells into leydig cell and myoid cell lineages

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Cited by 23 publications
(13 citation statements)
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“…In support of this possibility, Leydig cells in Older Group2 show higher expression of the Leydig/TPC progenitor cell markers, alongside lower expression of mature Leydig cell markers. We also observe clear reductions in HH receptors in aging Leydig cells and the weakened HH signaling interaction of Sertoli-Leydig cells; results in keeping with prior in vitro studies that HH signaling induces the common progenitor cells to differentiate into Leydig cells in rats (Zhao et al, 2021). Third, we observe TPC hyperplasia in aging testes-which is associated with less contractility and abnormal secretion of basement membrane components, factors that could impair the transport of sperm along the tubule as well as disrupting interactions between SSCs and the basement membrane.…”
Section: Aging Men With Elevated Bmi Are Molecularly and Phenotypical...supporting
confidence: 91%
“…In support of this possibility, Leydig cells in Older Group2 show higher expression of the Leydig/TPC progenitor cell markers, alongside lower expression of mature Leydig cell markers. We also observe clear reductions in HH receptors in aging Leydig cells and the weakened HH signaling interaction of Sertoli-Leydig cells; results in keeping with prior in vitro studies that HH signaling induces the common progenitor cells to differentiate into Leydig cells in rats (Zhao et al, 2021). Third, we observe TPC hyperplasia in aging testes-which is associated with less contractility and abnormal secretion of basement membrane components, factors that could impair the transport of sperm along the tubule as well as disrupting interactions between SSCs and the basement membrane.…”
Section: Aging Men With Elevated Bmi Are Molecularly and Phenotypical...supporting
confidence: 91%
“…A number of markers for LSCs had been previously suggested in human and nonhuman species. They include THY1 (CD90), CD51 (ITGAV), COUP-TFII (NR2F2), PDGFRA, TCF21 and Endoglein (ENG) [ 46 , 47 ]. These were readily detected, yet Nestin ( NES ) and ARX were not readily found.…”
Section: Resultsmentioning
confidence: 99%
“…However, we showed a significant reduction in the number of Leydig cells in adult testes only after fetal RAD exposure alone, although there was no decrease in the Leydig cell number in the neonatal testes. Adult Leydig cells arise from multiple progenitors, such as fetal Leydig cells, peritubular myoid cells and vascular pericytes, during puberty [54,55]. Analysis of the expression of distinct markers of adult and fetal Leydig cells such as Hsd3b6 or Cyp26b1, respectively [56,57], in adult testes suggests a common dysfunction of adult and "fetal" Leydig cells.…”
Section: Discussionmentioning
confidence: 99%