Diversity of proton pumps in osteoclasts: V-ATPase with a3 and d2 isoforms is a major form in osteoclasts

Biochim Biophys Acta. 2014 Jun;1837(6):744-9. doi: 10.1016/j.bbabio.2014.02.011. Epub 2014 Feb 19.

Abstract

Osteoclasts acidify bone resorption lacunae through proton translocation by plasma membrane V-ATPase (vacuolar-type ATPase) which has an a3 isoform, one of the four isoforms of the trans-membrane a subunit (Toyomura et al., J. Biol. Chem., 278, 22023-22030, 2003). d2, a kidney- and epididymis-specific isoform of the d subunit, was also induced in osteoclast-like cells derived from the RAW264.7 line, and formed V-ATPase with a3. The amount of d2 in osteoclasts was 4-fold higher than that of d1, a ubiquitous isoform. These results indicate that V-ATPase with d2/a3 is a major osteoclast proton pump. Essentially the same results were obtained with osteoclasts derived from mouse spleen macrophages. Macrophages from a3-knock-out mice could differentiate into multi-nuclear cells with osteoclast-specific enzymes. In these cells, the d2 isoform was also induced and assembled in V-ATPase with the a1 or a2 isoform. However, they did not absorb calcium phosphate, indicating that V-ATPase with d2/a1 or d2/a2 could not perform the function of that with d2/a3.

Keywords: Isoform; Osteoclast; Vacuolar-type ATPase; a3 knock out mouse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • DNA Primers
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Macrophages / enzymology
  • Mice
  • Mice, Knockout
  • Osteoclasts / enzymology
  • Osteoclasts / metabolism*
  • Polymerase Chain Reaction
  • Proton Pumps / metabolism*
  • Spleen / cytology
  • Spleen / enzymology
  • Vacuolar Proton-Translocating ATPases / genetics
  • Vacuolar Proton-Translocating ATPases / metabolism*

Substances

  • DNA Primers
  • Isoenzymes
  • Proton Pumps
  • Vacuolar Proton-Translocating ATPases