Male fertility defects in mice lacking the serine protease inhibitor protease nexin-1

Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3029-33. doi: 10.1073/pnas.051630698. Epub 2001 Feb 27.

Abstract

Understanding infertility and sterility requires knowledge of the molecular mechanisms underlying sexual reproduction. We have found that male mice deficient for the gene encoding the protease inhibitor protease nexin-1 (PN-1) show a marked impairment in fertility from the onset of sexual maturity. Absence of PN-1 results in altered semen protein composition, which leads to inadequate semen coagulation and deficient vaginal plug formation upon copulation. Progressive morphological changes of the seminal vesicles also are observed. Consistent with these findings, abnormal PN-1 expression was found in the semen of men displaying seminal dysfunction. The data demonstrate that the level of extracellular proteolytic activity is a critical element in controlling male fertility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Protein Precursor
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology*
  • Female
  • Humans
  • Infertility, Male / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Plasminogen Inactivators / physiology*
  • Protease Nexins
  • Receptors, Cell Surface
  • Semen / metabolism
  • Seminal Plasma Proteins / metabolism
  • Seminal Vesicles / metabolism
  • Serine Proteinase Inhibitors / physiology*
  • Serpin E2
  • Spermatozoa / metabolism
  • Spermatozoa / physiology
  • Vagina / physiology

Substances

  • Amyloid beta-Protein Precursor
  • Carrier Proteins
  • Plasminogen Inactivators
  • Protease Nexins
  • Receptors, Cell Surface
  • SERPINE2 protein, human
  • Seminal Plasma Proteins
  • Serine Proteinase Inhibitors
  • Serpin E2