AMH induces mesonephric cell migration in XX gonads

Mol Cell Endocrinol. 2003 Dec 15;211(1-2):1-7. doi: 10.1016/j.mce.2003.09.021.

Abstract

Migration of mesonephric cells into XY gonads is a critical early event in testis cord formation. Based on the fact that anti-Müllerian hormone (AMH) can induce testis cord formation in XX gonads, we investigated whether AMH plays a role in the induction of cell migration. Addition of recombinant AMH induced mesonephric migration into XX gonads in culture. AMH-treated XX gonads displayed increased vascular development and altered morphology of the coelomic epithelium, both features of normal testis differentiation. AMH did not induce markers of Sertoli or Leydig cell differentiation. We examined early testis development in Amh-deficient mice, but found no abnormalities, suggesting that any function AMH may have in vivo is redundant. Other transforming growth factor (TGF-beta) family proteins, bone morphogenetic proteins (BMP2 and BMP4) show similar inductive effects on XX gonads in culture. Although neither BMP2 nor BMP4 is expressed in embryonic XY gonads, our findings suggest that a TGF-beta signalling pathway endogenous to the XY gonad may be involved in regulation of mesonephric cell migration. The factors involved in this process remain to be identified.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anti-Mullerian Hormone
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Protein 4
  • Bone Morphogenetic Proteins / genetics
  • Bone Morphogenetic Proteins / pharmacology
  • Cell Movement / drug effects
  • Cell Movement / physiology*
  • Cholesterol Side-Chain Cleavage Enzyme / genetics
  • Coculture Techniques
  • Epithelium / anatomy & histology
  • Epithelium / drug effects
  • Female
  • Gene Expression Regulation, Developmental
  • Glycoproteins / genetics
  • Glycoproteins / pharmacology
  • Glycoproteins / physiology*
  • Gonads / drug effects
  • Gonads / embryology*
  • Gonads / metabolism
  • High Mobility Group Proteins / genetics
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Lac Operon / genetics
  • Laminin / analysis
  • Male
  • Mesonephros / cytology*
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Neovascularization, Physiologic / physiology
  • Organ Culture Techniques
  • Platelet Endothelial Cell Adhesion Molecule-1 / analysis
  • Receptors, Peptide / genetics
  • Receptors, Transforming Growth Factor beta
  • Recombinant Proteins / pharmacology
  • SOX9 Transcription Factor
  • Sex Differentiation / physiology
  • Testicular Hormones / genetics
  • Testicular Hormones / pharmacology
  • Testicular Hormones / physiology*
  • Transcription Factors / genetics
  • Transforming Growth Factor beta*
  • beta-Galactosidase / analysis

Substances

  • BMP2 protein, human
  • BMP4 protein, human
  • Bmp2 protein, mouse
  • Bmp4 protein, mouse
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Protein 4
  • Bone Morphogenetic Proteins
  • Glycoproteins
  • High Mobility Group Proteins
  • Laminin
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Receptors, Peptide
  • Receptors, Transforming Growth Factor beta
  • Recombinant Proteins
  • SOX9 Transcription Factor
  • SOX9 protein, human
  • Sox9 protein, mouse
  • Testicular Hormones
  • Transcription Factors
  • Transforming Growth Factor beta
  • anti-Mullerian hormone receptor
  • recombinant human bone morphogenetic protein-2
  • Anti-Mullerian Hormone
  • Cholesterol Side-Chain Cleavage Enzyme
  • beta-Galactosidase