Potential roles in cardiac physiology and pathology of the cation channel TRPV2 expressed in cardiac cells and cardiac macrophages: a mini-review

被引:21
作者
Entin-Meer, Michal [1 ]
Keren, Gad [1 ]
机构
[1] Tel Aviv Univ, Cardiovasc Res Lab, Tel Aviv Sourasky Med Ctr, Sackler Sch Med, Tel Aviv, Israel
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2020年 / 318卷 / 01期
关键词
acute myocardial infarction; cardiac macrophages; cardiomyocytes; dilated cardiomyopathy; TRPV2; VANILLOID; 2; RUTHENIUM RED; RECEPTOR; TRANSLOCATION; ACTIVATION; STRETCH; MOUSE; CARDIOMYOPATHY; INHIBITION; TRANILAST;
D O I
10.1152/ajpheart.00491.2019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
TRPV2 is a well-conserved channel protein expressed in almost all tissues. Cardiomyocyte TRPV2 is expressed in the intercalated disks of the cardiac sarcomeres, where it is involved in maintaining the proper mechanoelectric coupling and structure. It is also abundantly expressed in the intracellular pools, mainly the endoplasmic reticulum. Under pathological conditions, TRPV2 is translocated to the sarcolemma, where it mediates an abnormal [Ca](2+) entry that may contribute to disease progression. In addition, an intracellularly diffused TRPV2 expression is present in resident cardiac macrophages. Upon infection or inflammation, TRPV2 is engaged in early phagosomes and is, therefore, potentially involved in protecting the cardiac tissue. Following acute myocardial infarction, a profound elevated expression of TRPV2 is observed on the cell membrane of the peri-infarct macrophages. The macrophage TRPV2 may harbor a detrimental effect in cardiac recovery by increasing unfavorable migration and phagocytosis processes in the injured heart. Most reports suggest that while cardiac TRPV2 activation may be beneficial under specific physiological conditions, both cardiac- and macrophage-related TRPV2 blocking can significantly ameliorate disease progression in various pathological states. To verify this possibility, the time frame of TRPV2 overexpression and its mediated signaling need to be fully characterized in both cardiomyocyte and cardiac macrophage populations.
引用
收藏
页码:H181 / H188
页数:8
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