Differentiation and development of human female germ cells during prenatal gonadogenesis: an immunohistochemical study

Hum Reprod. 2005 Jun;20(6):1466-76. doi: 10.1093/humrep/deh800. Epub 2005 Feb 25.

Abstract

Background: In the development of the human ovary, the second trimester includes the transition from oogonial replication to primordial follicle formation. The present study was carried out to assess differentiation and proliferation of germ cells in a series of female gonads from 19 fetuses from the second and third trimester, and two neonates.

Methods: Using immunohistochemistry, the following markers were studied: placental/germ-like cell alkaline phosphatases (PLAP), the marker of pluripotency OCT3/4, the proliferation marker Ki-67, beta-catenin and E-cadherin, the stem cell factor receptor c-KIT, and VASA, a protein specific for the germ cell lineage.

Results: PLAP and OCT3/4 were seen during oogenesis, but not in germ cells engaged in folliculogenesis. A similar pattern was observed for Ki-67. Loss of pluripotency occurs once oocytes engage in follicle formation, suggesting a role of cell-cell interactions in the process of germ cell maturation. VASA, c-KIT, beta-catenin and E-cadherin were found in germ cells at all developmental stages of oogenesis and folliculogenesis.

Conclusions: Immunohistochemically, two groups of germ cells can be distinguished. Germ cells that are predominantly found in the cortical region of the ovary before weeks 22-24 of gestation, showing an immature phenotype, are mitotically active, and express OCT3/4, a marker of pluripotency. On the other hand, germ cells undergoing folliculogenesis have lost their pluripotent potential and no longer proliferate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Biomarkers / metabolism
  • Cadherins / metabolism
  • Cell Differentiation / physiology*
  • Cytoskeletal Proteins / metabolism
  • DEAD-box RNA Helicases
  • DNA-Binding Proteins / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Ki-67 Antigen / metabolism
  • Octamer Transcription Factor-3
  • Organic Cation Transport Proteins / metabolism
  • Ovary / cytology
  • Ovary / embryology*
  • Ovary / metabolism
  • Ovum / cytology*
  • Ovum / physiology
  • Pregnancy
  • Pregnancy Trimester, Second
  • Pregnancy Trimester, Third
  • Proto-Oncogene Proteins c-kit / metabolism
  • RNA Helicases / metabolism
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism
  • beta Catenin

Substances

  • Biomarkers
  • CTNNB1 protein, human
  • Cadherins
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • Ki-67 Antigen
  • Octamer Transcription Factor-3
  • Organic Cation Transport Proteins
  • POU5F1 protein, human
  • Trans-Activators
  • Transcription Factors
  • beta Catenin
  • solute carrier family 22 (organic cation transporter), member 3
  • Proto-Oncogene Proteins c-kit
  • Alkaline Phosphatase
  • DDX4 protein, human
  • DEAD-box RNA Helicases
  • RNA Helicases