Immunolocalization of Protein Kinase C Isoenzymes alpha, betaI, betaII and gamma in Adult and Developing Rat Kidney.
- Author:
Wan Young KIM
1
;
Gye Sil LEE
;
Young Hee KIM
;
Eun Young PARK
;
Jin Sun HWANG
;
Hyang KIM
;
Jin KIM
Author Information
- Publication Type:Original Article
- Keywords: Protein kinase C; Development; Kidney
- MeSH: Adult*; Animals; Biological Processes; Humans; Kidney*; Parturition; Protein Isoforms; Protein Kinase C beta; Protein Kinase C*; Protein Kinases*; Rats*; Signal Transduction; Ureter
- From:Electrolytes & Blood Pressure 2007;5(2):75-88
- CountryRepublic of Korea
- Language:English
- Abstract: Protein kinase C (PKC) plays an important role not only in signal transduction mechanisms in various biological processes, but also in the regulation of growth and differentiation during development. We studied the classical PKC alpha, betaI, betaII and gamma, with regard to their expression in adult and developing rat kidney. PKCalpha appeared in the ureteric bud at embryonic day (E) 16, and the proximal and distal anlage at E18. After birth, the immunoreactivity of PKCalpha gradually decreased. In adult, PKCalpha was expressed intensely in the connecting tubule (CNT), the collecting ducts (CD) and the renal corpuscle, and weakly in the proximal and distal tubules. PKCbetaI appeared in the ureteric bud at E16, and the proximal anlage at E18. After birth, the immunoreactivity of PKCbetaI gradually disappeared from the CD and proximal tubule. In adult, PKCbetaI was expressed in the intercalated cells of the CNT and cortical CD, the proximal straight tubule, and the renal corpuscle. PKCbII appeared in distal anlage at E18, and increased markedly after birth. In the CD, PKCbetaII immunoreactivity appeared after birth. In adult, PKCbetaII was expressed in the distal tubule, the CNT and the CD. The immunoreactivity for PKCgamma appeared only in the proximal anlage at E18, and increased temporally around the time of birth. However, no immunoreactivity for PKCgamma was observed in adult rat kidney. These results indicate that classical PKC isoforms appear to play a role in the regulation of various renal functions and differentiation within specific functional units of the uriniferous tubule in rat kidney.
