Tespa1 is a novel component of mitochondria-associated endoplasmic reticulum membranes and affects mitochondrial calcium flux.

Abstract

Regulation of intracellular Ca(2+) concentration is critical in numerous biological processes. Inositol 1,4,5-trisphosphate receptor (IP3R) functions as the Ca(2+) release channel on endoplasmic reticulum (ER) membranes. Much attention has been dedicated to mitochondrial Ca(2+) uptake via mitochondria-associated ER membranes (MAM) which is involved in intracellular Ca(2+) homeostasis; however, the molecular mechanisms that link the MAM to mitochondria still remain elusive. We previously reported that Tespa1 (thymocyte-expressed, positive selection-associated gene 1) expressed in lymphocytes physically interacts with IP3R. In this study, we first performed double-immunocytochemical staining of Tespa1 with a mitochondrial marker or an ER marker on an acute T lymphoblastic leukemia cell line, Jurkat cells, by using anti-ATP synthase or anti-calnexin antibody, respectively, and demonstrated that Tespa1 was localized very close to mitochondria and the Tespa1 localization was overlapped with restricted portion of ER. Next, we examined the effects of Tespa1 on the T cell receptor (TCR) stimulation-induced Ca(2+) flux by using Ca(2+) imaging in Jurkat cells. Reduction of Tespa1 protein by Tespa1-specific siRNA diminished TCR stimulation-induced Ca(2+) flux into both mitochondria and cytoplasm through the analyses of the mitochondrial Ca(2+) indicator (Rhod-2) and the cytoplasmic Ca(2+) indicator (Fluo-4), respectively. Furthermore, co-immunoprecipitation assay in HEK293 cells revealed that exogenous Tespa1 protein physically interacted with a MAM-associated protein, GRP75 (glucose-regulated protein 75), but not with an outer mitochondrial membrane protein, VDAC1 (voltage-dependent anion channel 1). All these results suggested that Tespa1 will participate in the molecular link between IP3R-mediated Ca(2+) release and mitochondrial Ca(2+) uptake in the MAM compartment.

• Authors: Hiroshi Matsuzaki, Takahiro Fujimoto, Masatoshi Tanaka, Senji Shirasawa
• Journal: Biochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 433 Issue 3 Pg. 322-6 (Apr 12 2013) ISSN: 1090-2104 [Electronic] United States
• PMID: 23501103 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2013 Elsevier Inc. All rights reserved.

Chemical References

• Adaptor Proteins, Signal Transducing
• Antibodies
• Biomarkers
• HSP70 Heat-Shock Proteins
• Inositol 1,4,5-Trisphosphate Receptors
• Membrane Proteins
• RNA, Small Interfering
• Receptors, Antigen, T-Cell
• TESPA1 protein, human
• VDAC1 protein, human
• glucose-regulated proteins
• Calnexin
• Voltage-Dependent Anion Channel 1
• Mitochondrial Proton-Translocating ATPases
• Calcium

Topics

• Adaptor Proteins, Signal Transducing (antagonists & inhibitors, genetics, metabolism)
• Antibodies (chemistry, immunology)
• Biomarkers (metabolism)
• Calcium (metabolism)
• Calnexin (genetics, metabolism)
• Endoplasmic Reticulum (metabolism, ultrastructure)
• Gene Expression Regulation
• Gene Silencing
• HEK293 Cells
• HSP70 Heat-Shock Proteins (genetics, metabolism)
• Humans
• Immunohistochemistry
• Inositol 1,4,5-Trisphosphate Receptors (genetics, metabolism)
• Intracellular Membranes (metabolism, ultrastructure)
• Ion Transport
• Jurkat Cells
• Membrane Proteins (genetics, metabolism)
• Mitochondria (metabolism, ultrastructure)
• Mitochondrial Proton-Translocating ATPases (genetics, metabolism)
• RNA, Small Interfering (genetics)
• Receptors, Antigen, T-Cell (antagonists & inhibitors, genetics, metabolism)
• Signal Transduction
• Voltage-Dependent Anion Channel 1 (genetics, metabolism)