Limitations of FKBP12.6-directed treatment strategies for maladaptive cardiac remodeling and heart failure

被引：16

作者：

Seidler, Tim ^{[1
]}

Teucher, Nils ^{[2
]}

Hellenkamp, Kristian ^{[1
]}

Unsoeld, Bernhard ^{[1
]}

Grebe, Cornelia ^{[1
]}

Kramps, Petra ^{[1
]}

Schotola, Hanna ^{[3
]}

Wagner, Stefan ^{[3
]}

Schoendube, Friedrich A. ^{[2
]}

Hasenfuss, Gerd ^{[1
]}

Maier, Lars S. ^{[1
]}

机构：

[1] Univ Gottingen, Dept Cardiol & Pneumol, Ctr Heart, D-37075 Gottingen, Germany

[2] Univ Gottingen, Dept Cardiac & Thorac & Cardiovasc Surg, Ctr Heart, D-37075 Gottingen, Germany

[3] Univ Gottingen, Dept Anesthesiol, Ctr Heart, D-37075 Gottingen, Germany

来源：

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY | 2011年 / 50卷 / 01期

关键词：

Transgenic mice; Maladaptive remodelling; Heart failure; FKBP; CaMK; Pressure overload; Ca sparks; Ca transients; CHANNEL RYANODINE RECEPTOR; FK506-BINDING PROTEIN FKBP12.6; SARCOPLASMIC-RETICULUM; FKBP12.6-MEDIATED STABILIZATION; PKA PHOSPHORYLATION; PRESSURE-OVERLOAD; RELEASE CHANNELS; CA2+ RELEASE; OVEREXPRESSION; MYOCYTES;

D O I：

10.1016/j.yjmcc.2010.08.016

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Sarcoplasmic reticulum (SR) calcium (Ca) leak can be reduced by enhancing FKBP12.6 binding to SR Ca release channels (RyR2) and expression of a "sticky" FKBP12.6(D37s) mutant may correct reduced binding stoichiometry in RyR2 from failing hearts. Both calcium/calmodulin-dependent protein kinase II delta c (CaMKII delta c) and protein kinase A (PKA) are activated in heart failure and promote SR Ca leak at RyR2. It is possible that FKBP12.6 dissociation from RyR2 may promote remodeling and that interventions to reassociate FKBP12.6 with RyR2 reflect a future therapeutic strategy. We created transgenic (TG) mice expressing FKBP12.6(D37s) and tested their capacity to improve intracellular Ca handling and pathological remodeling in vivo. FKBP12.6(D37S) TG mice were cross-bred with CaMKII delta c TG mice, which are known to exhibit pronounced RyR2 dysfunction and heart failure. We observed a significant improvement of post-rest Ca transients and a higher SR Ca content in FKBP12.6(D37S) TG mice. In double-TG mice, a marked reduction of SR Ca spark frequency indicated reduced SR Ca leak but neither SR Ca transient amplitude, SR Ca content nor morphological or functional parameters improved in vivo. Likewise, FKBP12.6(D37s) TG mice subjected to increased afterload after aortic banding exhibited higher SR Ca load but did not exhibit any improvement in hypertrophic growth or functional decline. Enhancement of FKBP12.6-RyR2 binding markedly reduced RyR2 Ca leak in CaMKII delta c-induced heart failure and in pressure overload. Our data suggest that activation of CaMKII delta c and pressure overload confer significant resistance towards approaches aiming at FKBP12.6-RyR2 reconstitution in heart failure and maladaptive remodeling, although RyR2 Ca leak can be reduced. (C) 2010 Elsevier Ltd. All rights reserved.

引用

页码：33 / 42

页数：10

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