Abstract

Ca(2+) and Ca(2+)-dependent signals are essential for sperm maturation and fertilization. In mouse sperm the plasma membrane Ca(2+)-ATPase (PMCA) isoform 4 plays a crucial role in Ca(2+) transport. The two major splice variants of PMCA4 are PMCA4a and PMCA4b. PMCA4a differs from PMCA4b in the mechanism of calmodulin binding and activation. PMCA4a shows a much higher basal activity and is more effective than PMCA4b in returning Ca(2+) to resting levels. Knock-out mice carrying a PMCA4-null mutation are infertile because their sperm cannot achieve a hyperactivated state of motility. As sperm reach functional maturity during their transit through the epididymis, the expression of PMCA4a and 4b was assessed in bull testis and epididymis. Quantitative PCR revealed that PMCA4b is the major splice variant in testis, caput, and corpus epididymidis. In contrast, PMCA4a is the major splice variant in cauda epididymidis, whereas sperm are transcriptionally silent. Immunohistochemical staining using a new antibody against bovine PMCA4a located the PMCA4a to the apical membrane of the epithelium of cauda epididymidis, whereas testis, caput, and corpus epididymidis were negative. Western blotting of testis, epididymis, and sperm isolated from caput and cauda epididymidis showed a much higher level of PMCA4a in cauda epididymidis and sperm from cauda epididymidis compared with testis membranes and sperm from caput epididymidis. These findings suggest that PMCA4a is transferred to bovine sperm membranes in cauda epididymidis. This isoform switch may facilitate a higher calcium turnover in sperm necessary to traverse the female genital tract.

Highlights

  • (PMCA1– 4) have been identified, each encoded by a separate gene

  • Sequence analysis of the 631-bp PCR product confirmed that it corresponds to the PMCA4 cDNA sequence from position 2895–3525 representing the PMCA4b splice variant

  • Whereas PMCA4b is the quantitatively major splice variant in caput and corpus, PMCA4a predominates in cauda epididymidis

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Summary

Introduction

(PMCA1– 4) have been identified, each encoded by a separate gene. By alternative splicing, Ͼ30 splice variants of the four PMCAs can be generated [4]. The various PMCA isoforms and splice variants show developmental-, tissue-, and cell-specific patterns of expression. We analyzed the gene and protein expression of PMCA4 in bull testis, epididymis, and sperm because this PMCA isoform is believed to be essential for sperm fertilization capacity. We found that the two PMCA splice variants 4a and 4b are differentially expressed with a shift from 4b to 4a along the length of the epididymis from caput to cauda. This suggests that functional sperm maturation requires a shift in calcium pump expression from the slow PMCA4b to the faster PMCA4a isoform

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