کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1930835 1050531 2011 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
KRAS-induced actin-interacting protein is required for the proper localization of inositol 1,4,5-trisphosphate receptor in the epithelial cells
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
KRAS-induced actin-interacting protein is required for the proper localization of inositol 1,4,5-trisphosphate receptor in the epithelial cells
چکیده انگلیسی

Three inositol 1,4,5-trisphosphate receptor (IP3R) subtypes are differentially expressed among tissues and function as the Ca2+ release channel on specialized endoplasmic reticulum (ER) membranes. The proper subcellular localization of IP3R is crucial for its proper function, but this molecular mechanism is unclear. KRAS-induced actin-interacting protein (KRAP) was originally identified as a cancer-related molecule, and is involved in the regulation of whole-body energy homeostasis and pancreatic exocrine system. We herein identified IP3R as an associated molecule with KRAP in vivo, and the association was validated by the co-immunoprecipitation and confocal immunostaining studies in mouse tissues including liver and pancreas. The association of KRAP with IP3R was also observed in the human epithelial cell lines including HCT116, HeLa and HEK293 cells. Intriguingly, KRAP interacts with distinct subtypes of IP3R in a tissue-dependent manner, i.e. IP3R1 and IP3R2 in the liver and IP3R2 and IP3R3 in the pancreas. The NH2-terminal amino acid residues 1–610 of IP3R are critical for the association with KRAP and KRAP–IP3R complex resides in a specialized ER but not a typical reticular ER. Furthermore, the localization of particular IP3R subtypes in tissues from KRAP-deficient mice is obviously disturbed, i.e. IP3R1 and IP3R2 in the liver and IP3R2 and IP3R3 in the pancreas. These findings demonstrate that KRAP physically associates with IP3R and regulates the proper localization of IP3R in the epithelial cells in vivo and cultured cells, and might shed light on the Ca2+ signaling underlying physiological cellular programs, cancer development and metabolism-related diseases.


► We identified IP3R as an associated protein with KRAP in vivo.
► KRAP interacts with distinct subtypes of IP3R in a tissue-dependent manner.
► KRAP–IP3R complex resides in a specialized endoplasmic reticulum.
► KRAP is required for the proper localization of IP3R in the epithelial cells.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 407, Issue 2, 8 April 2011, Pages 438–443
نویسندگان
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