在携带TPM1 E192K突变的患者中,丧失过桥抑制可导致病理性心肌肥大。

The Journal of General Physiology Pub Date : 2021-09-06 Epub Date: 2021-07-28 DOI:10.1085/jgp.202012640
Lorenzo R Sewanan, Jinkyu Park, Michael J Rynkiewicz, Alice W Racca, Nikolaos Papoutsidakis, Jonas Schwan, Daniel L Jacoby, Jeffrey R Moore, William Lehman, Yibing Qyang, Stuart G Campbell
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引用次数: 13

摘要

肥厚性心肌病(HCM)是一种遗传性疾病,主要由增厚和细丝蛋白突变引起。尽管细丝突变不像经常研究的粗丝突变那样普遍,但它们通常与严重的患者表型相关,并且可以为基本疾病机制提供重要的见解。我们对原肌球蛋白(TPM1) E192K进行了详细的研究,这是一种与HCM相关的不确定意义的变体。分子动力学显示E192K导致TPM1分子更灵活,这可能影响其调节交叉桥的能力。含有TPM1 E192K的调节肌动蛋白丝的体外运动测定显示Ca2+敏感性的整体丧失。为了理解这些影响,我们使用了多尺度计算模型,该模型表明E192K导致在低Ca2+时无法完全抑制肌动蛋白-肌球蛋白过桥活性的微妙表型。为了评估突变的生理影响,我们生成了表达E192K的患者来源的工程化心脏组织。这些组织表现出与患者相似的疾病特征,包括细胞肥大、过度收缩和舒张功能障碍。我们假设过量的剩余过桥活性可能触发细胞肥大,即使E192K降低了整体Ca2+敏感性。为了验证这一假设,将心肌肌球蛋白特异性抑制剂马伐camten应用于患者来源的工程化心脏组织4 d,然后进行24小时的冲洗。慢性马伐卡坦治疗消除了对照组和TPM1 E192K工程心脏组织之间的收缩差异,逆转了心肌细胞的肥大。这些结果表明,TPM1 E192K突变通过允许过量残留的过桥活性触发心肌细胞肥大。这些研究也提供了直接证据,表明马伐卡坦抑制肌球蛋白可以抵消突变原肌球蛋白的肥厚效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Loss of crossbridge inhibition drives pathological cardiac hypertrophy in patients harboring the TPM1 E192K mutation.

Loss of crossbridge inhibition drives pathological cardiac hypertrophy in patients harboring the TPM1 E192K mutation.

Loss of crossbridge inhibition drives pathological cardiac hypertrophy in patients harboring the TPM1 E192K mutation.

Loss of crossbridge inhibition drives pathological cardiac hypertrophy in patients harboring the TPM1 E192K mutation.

Hypertrophic cardiomyopathy (HCM) is an inherited disorder caused primarily by mutations to thick and thinfilament proteins. Although thin filament mutations are less prevalent than their oft-studied thick filament counterparts, they are frequently associated with severe patient phenotypes and can offer important insight into fundamental disease mechanisms. We have performed a detailed study of tropomyosin (TPM1) E192K, a variant of uncertain significance associated with HCM. Molecular dynamics revealed that E192K results in a more flexible TPM1 molecule, which could affect its ability to regulate crossbridges. In vitro motility assays of regulated actin filaments containing TPM1 E192K showed an overall loss of Ca2+ sensitivity. To understand these effects, we used multiscale computational models that suggested a subtle phenotype in which E192K leads to an inability to completely inhibit actin-myosin crossbridge activity at low Ca2+. To assess the physiological impact of the mutation, we generated patient-derived engineered heart tissues expressing E192K. These tissues showed disease features similar to those of the patients, including cellular hypertrophy, hypercontractility, and diastolic dysfunction. We hypothesized that excess residual crossbridge activity could be triggering cellular hypertrophy, even if the overall Ca2+ sensitivity was reduced by E192K. To test this hypothesis, the cardiac myosin-specific inhibitor mavacamten was applied to patient-derived engineered heart tissues for 4 d followed by 24 h of washout. Chronic mavacamten treatment abolished contractile differences between control and TPM1 E192K engineered heart tissues and reversed hypertrophy in cardiomyocytes. These results suggest that the TPM1 E192K mutation triggers cardiomyocyte hypertrophy by permitting excess residual crossbridge activity. These studies also provide direct evidence that myosin inhibition by mavacamten can counteract the hypertrophic effects of mutant tropomyosin.

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