Attenuated mesangial cell proliferation related to store-operated Ca2+ entry in aged rat: the role of STIM 1 and Orai 1

被引:20
作者
Shen, Bing [1 ]
Zhu, Jinhang [1 ]
Zhang, Jin [1 ]
Jiang, Feifei [1 ]
Wang, Zhaoyi [1 ]
Zhang, Yang [3 ]
Li, Jie [1 ]
Huang, Dake [2 ]
Ke, Daoping [1 ]
Ma, Rong [4 ]
Du, Juan [1 ]
机构
[1] Anhui Med Univ, Dept Physiol, Hefei, Peoples R China
[2] Anhui Med Univ, Comprehens Lab, Basic Med Sch, Hefei, Peoples R China
[3] Anhui Prov Hosp, Hefei 230032, Peoples R China
[4] Univ N Texas, Hlth Sci Ctr Ft Worth, Dept Integrat Physiol, Ft Worth, TX USA
基金
美国国家卫生研究院;
关键词
Aging; STIM; 1; Orai; Glomerular mesangial cell; Proliferation; STROMAL INTERACTION MOLECULE-1; PROTEIN-KINASE-C; CALCIUM INFLUX; ENDOPLASMIC-RETICULUM; CHANNELS; CRAC; HOMEOSTASIS; SENSOR; TRPC4;
D O I
10.1007/s11357-013-9511-5
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Store-operated Ca2+ entry (SOCE) is a common and ubiquitous mechanism regulating Ca2+ influx into cells and participates in numerous biological processes including cell proliferation. Glomerular mesangial cells (GMCs) play a role in the regulation of the glomerular filtration rate. From a clinical point of view, many physiological functions alter with age. In the present study, we used angiotensin II, glucagon, and the sarco/endoplasmic reticulum membrane Ca2+ pump inhibitor thapsigargin to deplete the internal Ca2+ stores for the activation of SOCE. We found that SOCE was significantly attenuated in GMCs from aged (22-month-old) rats. The expression of SOCE-related components, stromal interaction molecule 1 (STIM 1) and Orai 1, in freshly isolated glomeruli notably decreased, and STIM 1 and Orai 1 puncta formation significantly reduced in primary-cultured GMCs in aged rats. Moreover, specific knockdown of STIM 1 and Orai 1 by small interfering RNA markedly suppressed SOCE and cell proliferation of GMCs isolated from young (3-month-old) rats. We conclude that the attenuation of GMCs proliferation can be attributed to the decreased SOCE partially caused by reduced expression of STIM 1 and Orai 1.
引用
收藏
页码:2193 / 2202
页数:10
相关论文
共 40 条
[1]   Coupling of STIM1 to store-operated Ca2+ entry through its constitutive and inducible movement in the endoplasmic reticulum [J].
Baba, Yoshihiro ;
Hayashit, Kenji ;
Fujii, Yoko ;
Mizushima, Akiko ;
Watarai, Hiroshi ;
Wakamori, Minoru ;
Numaga, Takuro ;
Mori, Yasuo ;
Iino, Masamitsu ;
Hikida, Masaki ;
Kurosaki, Tomohiro .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (45) :16704-16709
[2]   Orais and STIMs: physiological mechanisms and disease [J].
Berna-Erro, A. ;
Woodard, G. E. ;
Rosado, J. A. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2012, 16 (03) :407-424
[3]   Ca2+ handling is altered when arterial myocytes progress from a contractile to a proliferative phenotype in culture [J].
Berra-Romani, Roberto ;
Mazzocco-Spezzia, Amparo ;
Pulina, Maria V. ;
Golovina, Vera A. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2008, 295 (03) :C779-C790
[4]   Calcium signalling: Dynamics, homeostasis and remodelling [J].
Berridge, MJ ;
Bootman, MD ;
Roderick, HL .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (07) :517-529
[5]   Orai1 (CRACM1) is the platelet SOC channel and essential for pathological thrombus formation [J].
Braun, Attila ;
Varga-Szabo, David ;
Kleinschnitz, Christoph ;
Pleines, Irina ;
Bender, Markus ;
Austinat, Madeleine ;
Boesl, Michael ;
Stoll, Guido ;
Nieswandt, Bernhard .
BLOOD, 2009, 113 (09) :2056-2063
[6]  
Christensen Mikkel, 2011, Rev Diabet Stud, V8, P369, DOI 10.1900/RDS.2011.8.369
[7]   Endoplasmic reticulum signaling as a determinant of recombinant protein expression [J].
Cudna, RE ;
Dickson, AJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (01) :56-65
[8]   Expression and relative abundance of short transient receptor potential channels in the rat renal microcirculation [J].
Facemire, CS ;
Mohler, PJ ;
Arendshorst, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 286 (03) :F546-F551
[9]   A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function [J].
Feske, S ;
Gwack, Y ;
Prakriya, M ;
Srikanth, S ;
Puppel, SH ;
Tanasa, B ;
Hogan, PG ;
Lewis, RS ;
Daly, M ;
Rao, A .
NATURE, 2006, 441 (7090) :179-185
[10]   Maintenance of calcium homeostasis in the endoplasmic reticulum by bcl-2 [J].
He, HL ;
Lam, M ;
McCormick, TS ;
Distelhorst, CW .
JOURNAL OF CELL BIOLOGY, 1997, 138 (06) :1219-1228