School of Biological Sciences, University of Reading, Reading, U.K.
Molecular and Clinical Sciences Institute, St. George's University of London, London, U.K.
Clin Sci (Lond). 2024 May 22;138(10):573-597. doi: 10.1042/CS20240496.
The three striatins (STRN, STRN3, STRN4) form the core of STRiatin-Interacting Phosphatase and Kinase (STRIPAK) complexes. These place protein phosphatase 2A (PP2A) in proximity to protein kinases thereby restraining kinase activity and regulating key cellular processes. Our aim was to establish if striatins play a significant role in cardiac remodelling associated with cardiac hypertrophy and heart failure. All striatins were expressed in control human hearts, with up-regulation of STRN and STRN3 in failing hearts. We used mice with global heterozygote gene deletion to assess the roles of STRN and STRN3 in cardiac remodelling induced by angiotensin II (AngII; 7 days). Using echocardiography, we detected no differences in baseline cardiac function or dimensions in STRN+/- or STRN3+/- male mice (8 weeks) compared with wild-type littermates. Heterozygous gene deletion did not affect cardiac function in mice treated with AngII, but the increase in left ventricle mass induced by AngII was inhibited in STRN+/- (but not STRN3+/-) mice. Histological staining indicated that cardiomyocyte hypertrophy was inhibited. To assess the role of STRN in cardiomyocytes, we converted the STRN knockout line for inducible cardiomyocyte-specific gene deletion. There was no effect of cardiomyocyte STRN knockout on cardiac function or dimensions, but the increase in left ventricle mass induced by AngII was inhibited. This resulted from inhibition of cardiomyocyte hypertrophy and cardiac fibrosis. The data indicate that cardiomyocyte striatin is required for early remodelling of the heart by AngII and identify the striatin-based STRIPAK system as a signalling paradigm in the development of pathological cardiac hypertrophy.
三种丝氨酸/苏氨酸激酶(STRN、STRN3、STRN4)构成 STR 相互作用磷酸酶和激酶(STRIPAK)复合物的核心。这些复合物将蛋白磷酸酶 2A(PP2A)置于蛋白激酶附近,从而抑制激酶活性并调节关键细胞过程。我们的目的是确定丝氨酸激酶是否在与心脏肥大和心力衰竭相关的心脏重塑中发挥重要作用。所有丝氨酸激酶在对照人心肌中均有表达,衰竭心脏中 STRN 和 STRN3 的表达上调。我们使用具有全局杂合基因缺失的小鼠来评估 STRN 和 STRN3 在血管紧张素 II(AngII;7 天)诱导的心脏重塑中的作用。通过超声心动图检测,我们发现 STRN+/-或 STRN3+/-雄性小鼠(8 周)与野生型同窝仔鼠相比,在基线心脏功能或尺寸上没有差异。杂合基因缺失不影响 AngII 处理的小鼠的心脏功能,但 AngII 诱导的左心室质量增加在 STRN+/-(而非 STRN3+/-)小鼠中受到抑制。组织学染色表明心肌细胞肥大受到抑制。为了评估 STRN 在心肌细胞中的作用,我们将 STRN 敲除系转化为诱导型心肌细胞特异性基因敲除系。心肌细胞 STRN 敲除对心脏功能或尺寸没有影响,但 AngII 诱导的左心室质量增加受到抑制。这是由于心肌细胞肥大和心脏纤维化的抑制。数据表明,心肌细胞丝氨酸激酶是 AngII 早期重塑心脏所必需的,并确定基于丝氨酸激酶的 STRIPAK 系统是病理性心肌肥大发展中的信号范例。