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The rat pkd2 protein assumes distinct subcellular distributions in different organs.
- Source :
-
The American journal of physiology [Am J Physiol] 1999 Dec; Vol. 277 (6), pp. F914-25. - Publication Year :
- 1999
-
Abstract
- Mutations in the PKD2 gene account for approximately 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.
- Subjects :
- Adrenal Glands cytology
Adrenal Glands metabolism
Animals
Calcium-Binding Proteins metabolism
Female
Humans
Immunohistochemistry
Kidney cytology
Kidney Cortex cytology
Kidney Cortex metabolism
Kidney Medulla cytology
Kidney Medulla metabolism
Kidney Tubules cytology
Kidney Tubules metabolism
Male
Membrane Proteins analysis
Membrane Proteins genetics
Muscle, Smooth, Vascular cytology
Muscle, Smooth, Vascular metabolism
Nephrons cytology
Nephrons metabolism
Organ Specificity
Ovary cytology
Ovary metabolism
Rats
Rats, Sprague-Dawley
Salivary Glands cytology
Salivary Glands metabolism
Submandibular Gland cytology
Submandibular Gland metabolism
TRPP Cation Channels
Kidney metabolism
Membrane Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0002-9513
- Volume :
- 277
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- The American journal of physiology
- Publication Type :
- Academic Journal
- Accession number :
- 10600939
- Full Text :
- https://doi.org/10.1152/ajprenal.1999.277.6.F914