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Am J Physiol Renal Physiol 291: F1052-F1060, 2006. First published May 30, 2006; doi:10.1152/ajprenal.00016.2006
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Expression of protein kinase C isoenzymes {alpha}, betaI, and {delta} in subtypes of intercalated cells of mouse kidney

Wan-Young Kim,1 Joon-Ho Jung,2 Eun-Young Park,1 Chul-Woo Yang,3 Hyang Kim,4 Søren Nielsen,5 Kirsten M. Madsen,6 and Jin Kim1

1Department of Anatomy and Medical Research Center for Cell Death Disease Research Center, 3Department of Internal Medicine, College of Medicine, The Catholic University of Korea, 2Department of Urology, Bundang Jesang Hospital, and 4Department of Internal Medicine, Sungkyunkwan University, Kangbuk Samsung Hospital, Seoul, Korea; 5The Water and Salt Research Center, University of Aarhus, Aarhus, Denmark; and 6Department of Medicine, University of Florida, Gainesville, Florida

Submitted 19 January 2006 ; accepted in final form 26 May 2006

Recent studies of the distribution of PKC isoenzymes in the mouse kidney demonstrated that PKC-{alpha}, -betaI, and -{delta} are expressed in intercalated cells. The purpose of this study was to identify the intercalated cell subtypes that express the different PKC isoenzymes and determine the location of the PKC isoenzymes within these cells. Adult C57BL/6 mice kidney tissues were processed for multiple-labeling immunohistochemistry. Antibodies against the vacuolar H+-ATPase and pendrin were used to identify intercalated cell subtypes, whereas antibodies against calbindin D28K and aquaporin-2 (AQP2) were used to identify connecting tubule cells and principal cells of the collecting duct, respectively. Within type A intercalated cells, PKC-{delta} was highly expressed in the apical part of the cells, whereas immunoreactivity for both PKC-{alpha} and PKC-betaI was weak. Type B intercalated cells exhibited strong expression of PKC-{alpha}, -betaI, and -{delta}. PKC-{alpha} and -betaI were localized throughout the cytoplasm, whereas PKC-{delta} was restricted to the basal domain. Within non-A-non-B cells, immunoreactivity for both PKC-{alpha} and PKC-betaI was high in intensity and localized diffusely in the cytoplasm, whereas PKC-{delta} was localized in the apical part of the cells. None of the PKC isoenzymes (PKC-{alpha}, -betaI, or -{delta}) were expressed in the calbindin D28K-positive connecting tubule cells. Within AQP2-positive principal cells of the collecting duct, PKC-{alpha} was expressed on the basolateral plasma membrane, but no significant staining was detected for PKC-betaI and -{delta}. In summary, this study demonstrates distinct and differential expression patterns of PKC-{alpha}, -betaI, and -{delta} in the three subtypes of intercalated cells in the mouse kidney.

PKC-{alpha}; -betaI; and -{delta}; immunohistochemistry



Address for reprint requests and other correspondence: J. Kim, Dept. of Anatomy and MRC for Cell Death Disease Research Center, College of Medicine, The Catholic Univ. of Korea, Seoul, Korea, 505, Banpo-Dong, Seocho-Ku, Seoul 137–701, Korea (e-mail: jinkim{at}catholic.ac.kr)




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Angiotensin II Stimulates Vacuolar H+-ATPase Activity in Renal Acid-Secretory Intercalated Cells from the Outer Medullary Collecting Duct
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[Abstract] [Full Text] [PDF]




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