Mapping lineage progression of somatic progenitor cells in the mouse fetal testis

Development. 2016 Oct 15;143(20):3700-3710. doi: 10.1242/dev.135756. Epub 2016 Sep 12.

Abstract

Testis morphogenesis is a highly orchestrated process involving lineage determination of male germ cells and somatic cell types. Although the origin and differentiation of germ cells are known, the developmental course specific for each somatic cell lineage has not been clearly defined. Here, we construct a comprehensive map of somatic cell lineage progression in the mouse testis. Both supporting and interstitial cell lineages arise from WT1+ somatic progenitor pools in the gonadal primordium. A subpopulation of WT1+ progenitor cells acquire SOX9 expression and become Sertoli cells that form testis cords, whereas the remaining WT1+ cells contribute to progenitor cells in the testis interstitium. Interstitial progenitor cells diversify through the acquisition of HES1, an indication of Notch activation, at the onset of sex determination. HES1+ interstitial progenitors, through the action of Sertoli cell-derived Hedgehog signals, become positive for GLI1. The GLI1+ interstitial cells eventually develop into two cell lineages: steroid-producing fetal Leydig cells and non-steroidogenic cells. The fetal Leydig cell population is restricted by Notch2 signaling from the neighboring somatic cells. The non-steroidogenic progenitor cells retain their undifferentiated state during fetal stage and become adult Leydig cells in post-pubertal testis. These results provide the first lineage progression map that illustrates the sequential establishment of somatic cell populations during testis morphogenesis.

Keywords: Hedgehog; Leydig cells; Lineage specification; Notch; Sertoli cells; Testis.

MeSH terms

  • Adult Stem Cells / cytology*
  • Adult Stem Cells / metabolism
  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Gene Expression Regulation, Developmental / genetics
  • Gene Expression Regulation, Developmental / physiology
  • Immunohistochemistry
  • Leydig Cells / cytology
  • Leydig Cells / metabolism
  • Male
  • Mice
  • Sertoli Cells / cytology
  • Sertoli Cells / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Stem Cells / cytology*
  • Stem Cells / metabolism*
  • Tamoxifen / pharmacology
  • Testis / embryology*
  • Testis / metabolism*
  • Transcription Factor HES-1 / genetics
  • Transcription Factor HES-1 / metabolism
  • Zinc Finger Protein GLI1 / genetics
  • Zinc Finger Protein GLI1 / metabolism

Substances

  • Gli1 protein, mouse
  • Hes1 protein, mouse
  • Transcription Factor HES-1
  • Zinc Finger Protein GLI1
  • Tamoxifen