Mice carrying a conditional Serca2flox allele for the generation of Ca2+ handling-deficient mouse models

被引:30
作者
Andersson, Kristin B. [1 ,2 ]
Finsen, Alexandra V. [1 ,2 ]
Sjaland, Cecilie [1 ,2 ]
Winer, Lisbeth H. [1 ,2 ]
Sjaastad, Ivar [1 ,2 ]
Odegaard, Annlaug [1 ,2 ]
Louch, William E. [1 ,2 ]
Wang, Yibin [3 ,4 ,5 ]
Chen, Ju [6 ]
Chien, Kenneth R. [7 ]
Sejersted, Ole M. [1 ,2 ]
Christensen, Geir [1 ,2 ]
机构
[1] Univ Oslo, Ullevaal Hosp, Expt Med Res Inst, N-0407 Oslo, Norway
[2] Univ Oslo, Ctr Heart Failure Res, N-0407 Oslo, Norway
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Anesthesiol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[6] Univ Calif San Diego, Sch Med, La Jolla, CA 92093 USA
[7] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
关键词
Serca2; Calcium ATPase; Endoplasmic reticulum; Sarcoplasmic reticulum; Flax; Transgenic mouse; SARCOPLASMIC-RETICULUM CA2+-ATPASE; CONGESTIVE-HEART-FAILURE; CARDIAC-PERFORMANCE; DARIERS-DISEASE; CALCIUM; MUSCLE; EXPRESSION; TRANSPORT; SERCA2A; GENE;
D O I
10.1016/j.ceca.2009.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sarco(endo)plasmic reticulum calcium ATPases (SERCA) are cellular pumps that transport Ca2+ into the sarcoplasmic reticulum (SR). Serca2 is the most widely expressed gene family member. The very early embryonic lethality of Serca2(null) mouse embryos has precluded further evaluation of loss of Serca2 function in the context of organ physiology. We have generated mice carrying a conditional Serca2(flox) allele which allows disruption of the Serca2 gene in an organ-specific and/or inducible manner. The model was tested by mating Serca2(flox) mice with MLC-2v(wt/cre) mice and with alpha MHC-Cre transgenic mice. In heterozygous Serca2(wt/flox)MLC-2v(wt/Cre) mice. the expression of SERCA2a and SERCA2b proteins were reduced in the heart and slow skeletal muscle. in accordance with the expression pattern of the MLC-2v gene. In Serca2(flox/flox) Tg(alpha MHC-Cre) embryos with early homozygous cardiac Serca2 disruption, normal embryonic development and yolk sac circulation was maintained up to at least embryonic stage E10.5. The Serca2(flox) mouse is the first murine conditional gene disruption model for the SERCA family of Ca2+ ATPases, and should be a powerful tool for investigating specific physiological roles of SERCA2 function in a range of tissues and organs in vivo both in adult and embryonic stages. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:219 / 225
页数:7
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