In addition to the three isoforms of the catalytic subunit of the Na,K-ATPa
se originally identified (alpha 1, alpha 2, and alpha 3), a fourth a polype
ptide (alpha 4) has recently been found in mammalian cells. This novel a-su
bunit of the Na, K-ATPase is selectively expressed in male gonadal tissues.
In the testes, alpha 4 is functionally active and comprises approximately
half of the Na,K-ATPase activity of the organ. At present, the pattern of e
xpression of the alpha 4 polypeptide within the cells of the male gonad is
unknown. By in situ hybridization, immunocytochemistry, and the ouabain inh
ibition profile of Na,K ATPase activity, we show that the alpha 4-subunit i
s expressed in the germ cells of rat testes. The highest amounts of the iso
form are found in spermatozoa, where it constitutes two thirds of the Na,K-
ATPase activity of the gametes. The other Na pump present in the cells is t
he ubiquitously expressed alpha 1 polypeptide. The characteristic localizat
ion of alpha 4 in the gonad is further supported by the drastic reduction o
f the polypeptide in mice that are infertile as a consequence of arrest in
maturation of the germ cells. In addition, GC-1spg cells, a murine cell lin
e derived from testis spermatogonia, also contain the Na,K-ATPase alpha 4 p
olypeptide. However, the level of expression of the isoform in these cells
is much lower than in the spermatozoa, a fact that may depend on the limite
d ability of the GC-1spg cells to differentiate in vitro. The particular ex
pression of the Na,K-ATPase alpha 4 isoform we encounter and the specific e
nzymatic properties of the polypeptide suggests its importance for ionic ho
meostasis of the germ cells of the testes.