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Pituitary Expression of Protein Kinase C Isotypes During Early Development
Author(s) -
Korytko Andrew I.,
Fields Alan P.,
Allshouse Lisa A.,
Cuttler Leona
Publication year - 1998
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1046/j.1365-2826.1998.00201.x
Subject(s) - protein kinase c , gonadotropic cell , medicine , endocrinology , somatotropic cell , immunohistochemistry , biology , pituitary gland , signal transduction , hormone , microbiology and biotechnology
Protein kinase C (PKC) is a critical regulator of signal transduction and cell function in many tissues, including pituitary. Although PKC influences pituitary hormone secretion in adults, its role in determining characteristic perinatal patterns of hormone secretion and synthesis is not known, and the expression of major PKC isotypes in perinatal pituitary is poorly defined. We therefore determined the developmental, cell‐specific expression of the major PKC isotypes, using Western analysis and double label immunohistochemistry, in pituitaries of perinatal and mature rats. Expression of specific PKC isotypes was strikingly age‐dependent. Pituitary expression of PKC α was particularly high in neonates and declined significantly with age, with levels in adult rats approximately half those of neonates as assessed by Western analysis. Similarly, immunohistochemistry indicated that PKC α was less abundant in adult than in neonatal pituitaries; the most intensely staining cells of both age groups were identified as somatotrophs and gonadotrophs. In contrast to PKC α , pituitary expression of PKC ε increased approximately two‐fold with advancing age as assessed by Western analysis; this age‐dependent pattern was confirmed by immunohistochemistry. Perinatal pituitaries expressed PKC ε in some somatotrophs and in all gonadotrophs, whereas PKC ε expression was limited to gonadotrophs in the mature pituitary. Pituitary expression of PKC β II, δ , and ζ did not differ with age, and PKC γ was not detected in pituitaries of any age group. These results indicate that expression of PKC isotypes within the pituitary is developmentally regulated in a cell‐specific and isotype‐specific manner, and are consistent with the concept that PKC contributes to the regulation of pituitary function during early development.

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