The rat Pkd2 protein assumes distinct subcellular distributions in different organs

被引:35
作者
Obermüller, N
Gallagher, AR
Cai, YQ
Gassler, N
Gretz, N
Somlo, S
Witzgall, R
机构
[1] Heidelberg Univ, Inst Anat & Cell Biol 1, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Klinikum Mannheim, Med Res Ctr, D-68167 Mannheim, Germany
[3] Yale Univ, Sch Med, Nephrol Sect, New Haven, CT 06520 USA
[4] Heidelberg Univ, Dept Pathol, D-69120 Heidelberg, Germany
关键词
polycystic kidney disease; immunohistochemistry; endoplasmic reticulum;
D O I
10.1152/ajprenal.1999.277.6.F914
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Mutations in the PKD2 gene account for similar to 15% of all cases of autosomal-dominant polycystic kidney disease. In the present study the cellular distribution of the Pkd2 protein was investigated by immunohistochemistry in different rat organs. Although the Pkd2 protein showed a widespread expression, a strikingly different distribution of the protein was observed between individual organs. Whereas in renal distal tubules and in striated ducts of salivary glands a basal-to-basolateral distribution of Pkd2 was found, a punctate cytoplasmic location was detected in the adrenal gland, ovary, cornea, and smooth muscle cells of blood vessels. Interestingly, in the adrenal gland and ovary, the rat Pkd2 protein was more heavily N-glycosylated than in the kidney and salivary gland. These results suggest that Pkd2 accomplishes its functions by interacting with proteins located in different cellular compartments. The extrarenal expression pattern of the Pkd2 protein hints at other candidate sites of disease manifestations in patients carrying PKD2 mutations.
引用
收藏
页码:F914 / F925
页数:12
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