Fibrocystin/polyductin, found in the same protein complex with polycystin-2, regulates calcium responses in kidney epithelia.

Abstract

Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC2) are all localized at the plasma membrane and the primary cilium, where PC1 and PC2 contribute to fluid flow sensation and may function in the same mechanotransduction pathways. To further define the exact subcellular localization of FPC, the protein product encoded by the PKHD1 gene responsible for autosomal recessive polycystic kidney disease (PKD) in humans, and whether FPC has direct and/or indirect cross talk with PC2, which, in turn, is pivotal for the pathogenesis of autosomal dominant PKD, we performed double immunostaining and coimmunoprecipitation as well as a microfluorimetry study of kidney tubular epithelial cells. FPC and PC2 are found to completely or partially colocalize at the plasma membrane and the primary cilium and can be reciprocally coimmunoprecipitated. Although incomplete removal of FPC by small interfering RNA and antibody 803 to intracellular epitopes of FPC did not abolish flow-induced intracellular calcium responses, antibody 804 to extracellular epitopes of FPC blocked cellular calcium responses to flow stimulation. These findings suggest that FPC and polycystins share, at least in part, a common mechanotransduction pathway.

• Authors: Shixuan Wang, Jingjing Zhang, Surya M Nauli, Xiaogang Li, Patrick G Starremans, Ying Luo, Kristina A Roberts, Jing Zhou
• Journal: Molecular and cellular biology (Mol Cell Biol) Vol. 27 Issue 8 Pg. 3241-52 (Apr 2007) ISSN: 0270-7306 [Print] United States
• PMID: 17283055 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Antibodies
• PKHD1 protein, human
• Pkhd1 protein, mouse
• Receptors, Cell Surface
• TRPP Cation Channels
• polycystic kidney disease 1 protein
• polycystic kidney disease 2 protein
• Calcium

Topics

• Animals
• Antibodies (pharmacology)
• Calcium (metabolism, pharmacology)
• Cell Membrane (drug effects, metabolism)
• Cells, Cultured
• Cilia (drug effects, metabolism)
• Cytosol (drug effects)
• Dogs
• Epithelial Cells (cytology, drug effects, metabolism)
• Humans
• Immunoprecipitation
• Kidney Tubules (cytology, drug effects, metabolism)
• Mice
• Protein Binding (drug effects)
• Protein Transport (drug effects)
• Receptors, Cell Surface (metabolism)
• Shear Strength
• TRPP Cation Channels (metabolism)