Alignment of sarcoplasmic reticulum-mitochondrial junctions with mitochondrial contact points

被引:54
作者
Garcia-Perez, Cecilia [1 ]
Schneider, Timothy G. [1 ]
Hajnoczky, Gyoergy [1 ]
Csordas, Gyoergy [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2011年 / 301卷 / 05期
关键词
Ca2+ signaling; cardiac muscle; tethering; mitofusin; 2; ENDOPLASMIC-RETICULUM; CALCIUM UNIPORTER; CA2+; SITES; MEMBRANE; HEART; ER; MITOFUSINS; CROSSTALK; APOPTOSIS;
D O I
10.1152/ajpheart.00397.2011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Garcia-Perez C, Schneider TG, Hajnoczky G, Csordas G. Alignment of sarcoplasmic reticulum-mitochondrial junctions with mitochondrial contact points. Am J Physiol Heart Circ Physiol 301: H1907-H1915, 2011. First published August 19, 2011; doi:10.1152/ajpheart.00397.2011.-Propagation of ryanodine receptor (RyR2)-derived Ca2+ signals to the mitochondrial matrix supports oxidative ATP production or facilitates mitochondrial apoptosis in cardiac muscle. Ca2+ transfer likely occurs locally at focal associations of the sarcoplasmic reticulum (SR) and mitochondria, which are secured by tethers. The outer mitochondrial membrane and inner mitochondrial membrane (OMM and IMM, respectively) also form tight focal contacts (contact points) that are enriched in voltage-dependent anion channels, the gates of OMM for Ca2+. Contact points could offer the shortest Ca2+ transfer route to the matrix; however, their alignment with the SR-OMM associations remains unclear. Here, in rat heart we have studied the distribution of mitochondria-associated SR in submitochondrial membrane fractions and evaluated the colocalization of SR-OMM associations with contact points using transmission electron microscopy. In a sucrose gradient designed for OMM purification, biochemical assays revealed lighter fractions enriched in OMM only and heavier fractions containing OMM, IMM, and SR markers. Pure OMM fractions were enriched in mitofusin 2, an similar to 80 kDa mitochondrial fusion protein and SR-mitochondrial tether candidate, whereas in fractions of OMM + IMM + SR, a lighter (similar to 50 kDa) band detected by antibodies raised against the NH2 terminus of mitofusin 2 was dominating. Transmission electron microscopy revealed mandatory presence of contact points at the junctional SR-mitochondrial interface versus a random presence along matching SR-free OMM segments. For each SR-mitochondrial junction at least one tether was attached to contact points. These data establish the contact points as anchorage sites for the SR-mitochondrial physical coupling. Close coupling of the SR, OMM, and IMM is likely to provide a favorable spatial arrangement for local ryanodine receptor-mitochondrial Ca2+ signaling.
引用
收藏
页码:H1907 / H1915
页数:9
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