Co-localization of the inositol 1,4,5-trisphosphate receptor and calreticulin in the equatorial segment and in membrane bounded vesicles in the cytoplasmic droplet of human spermatozoa

Mol Hum Reprod. 2001 Oct;7(10):923-33. doi: 10.1093/molehr/7.10.923.

Abstract

Modulation of the intracellular calcium concentration within mammalian spermatozoa is important in several pre-fertilization events including hyperactivated motility and the acrosome reaction. To identify calcium binding proteins (CBP) potentially regulating these processes, a (45)Ca overlay technique was employed on 2-D blots of human sperm extracts. Microsequencing by Edman degradation and CAD mass spectrometry identified a relatively abundant 60.5 kDa CBP with a pI of 4.2 as calreticulin (CRT). Immunofluorescent labelling with anti-CRT antibodies localized CRT to the acrosome, with highest fluorescence in the equatorial segment, and in the cytoplasmic droplets of 94 and 48% of human spermatozoa respectively. Double immunolabelling experiments demonstrated co-localization of CRT and the inositol 1,4,5-trisphosphate receptor (IP(3)R) in the acrosome, in the equatorial segment, and vesicular structures in the cytoplasmic droplets of the neck region. Electron microscopic immunogold labelling localized CRT to the equatorial segment of acrosome-reacted spermatozoa and to membrane-enclosed vesicles within the cytoplasmic droplet of both acrosome-intact and acrosome-reacted spermatozoa. Localization of the IP(3) receptor to the CRT-containing vesicles, in the sperm neck and to the acrosome, suggests that capacitative calcium entry in human spermatozoa may be regulated from these putative calcium storage sites.

Publication types

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

MeSH terms

  • Acrosome / metabolism
  • Blotting, Northern
  • Calcium / metabolism
  • Calcium Channels / immunology
  • Calcium Channels / metabolism*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / immunology
  • Calcium-Binding Proteins / metabolism*
  • Calreticulin
  • Cell Membrane / metabolism
  • Cytoplasmic Vesicles / metabolism*
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors
  • Male
  • Microscopy, Immunoelectron
  • Organ Specificity
  • Receptors, Cytoplasmic and Nuclear / immunology
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / immunology
  • Ribonucleoproteins / metabolism*

Substances

  • Calcium Channels
  • Calcium-Binding Proteins
  • Calreticulin
  • ITPR1 protein, human
  • Inositol 1,4,5-Trisphosphate Receptors
  • Receptors, Cytoplasmic and Nuclear
  • Ribonucleoproteins
  • Calcium