首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Muscle Diversity Heterogeneity and Gradients: Learning from Sarcoglycanopathies
【2h】

Muscle Diversity Heterogeneity and Gradients: Learning from Sarcoglycanopathies

机译:肌肉多样性异质性和梯度:从疯狂的过程中学习

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Skeletal muscle, the most abundant tissue in the body, is heterogeneous. This heterogeneity forms the basis of muscle diversity, which is reflected in the specialized functions of muscles in different parts of the body. However, these different parts are not always clearly delimitated, and this often gives rise to gradients within the same muscle and even across the body. During the last decade, several studies on muscular disorders both in mice and in humans have observed particular distribution patterns of muscle weakness during disease, indicating that the same mutation can affect muscles differently. Moreover, these phenotypical differences reveal gradients of severity, existing alongside other architectural gradients. These two factors are especially prominent in sarcoglycanopathies. Nevertheless, very little is known about the mechanism(s) driving the phenotypic diversity of the muscles affected by these diseases. Here, we will review the available literature on sarcoglycanopathies, focusing on phenotypic differences among affected muscles and gradients, characterization techniques, molecular signatures, and cell population heterogeneity, highlighting the possibilities opened up by new technologies. This review aims to revive research interest in the diverse disease phenotype affecting different muscles, in order to pave the way for new therapeutic interventions.
机译:骨骼肌,身体中最丰富的组织,是异质的。这种异质性构成了肌肉变化的基础,这反映在身体不同部位的肌肉的专业功能中。然而,这些不同的部件并不总是明确限制,这通常会导致同一肌肉中的梯度,甚至穿过身体。在过去的十年中,小鼠和人类患者患有肌肉障碍的几项研究已经观察到疾病期间肌肉无力的特定分布模式,表明相同的突变可以不同地影响肌肉。此外,这些表型差异揭示了严重程度,与其他建筑梯度一起存在。这两种因素在疯狂的过程中尤其突出。然而,关于驱动受这些疾病影响的肌肉的表型多样性的机制很少。在这里,我们将审查Sarcoglycanopaties的可用文献,重点关注受影响的肌肉和梯度,表征技术,分子签名和细胞群体异质性的表型差异,突出了新技术开放的可能性。本综述旨在恢复影响不同肌肉的多种疾病表型的研究兴趣,以便为新的治疗干预措施铺平道路。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号