Title

Specific testicular cellular localization and hormonal regulation of the PKIα and PKIß isoforms of the inhibitor protein of the cAMP-dependent protein kinase

Document Type

Article

Publication Date

1997

Abstract

We have previously demonstrated that there exist two distinct genes for the thermostable inhibitor protein of the cAMP-dependent protein kinase, PKIα and PKIß (Van Patten, S. M., Howard, P., Walsh, D. A., and Maurer. R. A. (1992) Mol. Endocrinol 6, 2114-2122). We have also shown that in the testis, at least eight forms of PKIß exist, differing as a result of at least post-translational modification and alternate translational initiation (Kumar, P., Van Patten, S. M., and Walsh, D. A. (1997) J. Biol. Chem. 272, 20011-20020). We now report that in the testis, there is a unique cellular distribution of protein kinase inhibitor forms, with PKIß being essentially (if not exclusively) a germ cell protein and PKIα being expressed primarily in Sertoli cells. Furthermore, there is a progressive change in the forms of PKIß that are present within germ cells with development that is initiated in testis tubules and continues as the germ cells migrate through the epididymis. These conclusions are derived from studies with isolated cell populations and with the at/at germ cell-deficient mouse line, by in situ hybridization, and by following the developmental expression of these proteins in both testis and epididymis. We have also shown that follicle- stimulating hormone (FSH) can increase the expression of both PKIα and PKIß. The FSH-regulated expression of PKIα in the Sertoli cell likely occurs via the normal route of second messenger signal transduction. In contrast, the FSH-dependent PKIß expression must arise by some form of Sertoli cell-germ cell intercommunication.

Publication Title

Journal of Biological Chemistry

Volume

272

Issue

32

First Page

20021

Last Page

20029

Comments

This article was published in Journal of Biological Chemistry, Volume 272, Issue 32, Pages 20021-20029.

The published version is available at http://dx.doi.org/10.1074/jbc.272.32.20021.

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