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在一项针对钙调神经磷酸酶信号通路调节剂的化学筛选中发现的一种心脏肥大小分子激活剂。

A small molecular activator of cardiac hypertrophy uncovered in a chemical screen for modifiers of the calcineurin signaling pathway.

作者信息

Bush Erik, Fielitz Jens, Melvin Lawrence, Martinez-Arnold Michael, McKinsey Timothy A, Plichta Ryan, Olson Eric N

机构信息

Myogen, Incorporated, Westminster, CO 80021, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):2870-5. doi: 10.1073/pnas.0308723101. Epub 2004 Feb 19.

Abstract

The calcium, calmodulin-dependent phosphatase calcineurin, regulates growth and gene expression of striated muscles. The activity of calcineurin is modulated by a family of cofactors, referred to as modulatory calcineurin-interacting proteins (MCIPs). In the heart, the MCIP1 gene is activated by calcineurin and has been proposed to fulfill a negative feedback loop that restrains potentially pathological calcineurin signaling, which would otherwise lead to abnormal cardiac growth. In a high-throughput screen for small molecules capable of regulating MCIP1 expression in muscle cells, we identified a unique 4-aminopyridine derivative exhibiting an embedded partial structural motif of serotonin (5-hydroxytryptamine, 5-HT). This molecule, referred to as pyridine activator of myocyte hypertrophy, acts as a selective agonist for 5-HT(2A/2B) receptors and induces hypertrophy of cardiac muscle cells through a signaling pathway involving calcineurin and a kinase-dependent mechanism that inactivates class II histone deacetylases, which act as repressors of cardiac growth. These findings identify MCIP1 as a downstream target of 5-HT(2A/2B) receptor signaling in cardiac muscle cells and suggest possible uses for 5-HT(2A/2B) agonists and antagonists as modulators of cardiac growth and gene expression.

摘要

钙调神经磷酸酶是一种依赖于钙和钙调蛋白的磷酸酶,可调节横纹肌的生长和基因表达。钙调神经磷酸酶的活性受一类辅因子调节,这类辅因子被称为钙调神经磷酸酶调节相互作用蛋白(MCIPs)。在心脏中,MCIP1基因由钙调神经磷酸酶激活,有人提出它可形成一个负反馈环,抑制潜在的病理性钙调神经磷酸酶信号传导,否则会导致心脏异常生长。在一项针对能够调节肌肉细胞中MCIP1表达的小分子的高通量筛选中,我们鉴定出一种独特的4-氨基吡啶衍生物,它具有5-羟色胺(5-羟色胺,5-HT)的部分嵌入结构基序。这种分子被称为心肌肥大吡啶激活剂,作为5-HT(2A/2B)受体的选择性激动剂,通过一条涉及钙调神经磷酸酶和激酶依赖性机制的信号通路诱导心肌细胞肥大,该机制可使II类组蛋白去乙酰化酶失活,而II类组蛋白去乙酰化酶是心脏生长的抑制因子。这些发现确定MCIP1是心肌细胞中5-HT(2A/2B)受体信号传导的下游靶点,并提示5-HT(2A/2B)激动剂和拮抗剂可能作为心脏生长和基因表达调节剂的用途。

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