3D-environment and muscle contraction regulate the heterogeneity of myonuclei.

IF 5.3 2区 医学 Q2 CELL BIOLOGY
Rosa Nicolas, Marie-Ange Bonnin, Cédrine Blavet, Joana Esteves de Lima, Cécile Legallais, Delphine Duprez
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Abstract

Skeletal muscle formation involves tight interactions between muscle cells and associated connective tissue fibroblasts. Every muscle displays the same type of organisation, they are innervated in the middle and attached at both extremities to tendons. Myonuclei are heterogeneous along myotubes and regionalised according to these middle and tip domains. During development, as soon as myotubes are formed, myonuclei at muscle tips facing developing tendons display their own molecular program. In addition to molecular heterogeneity, a subset of tip myonuclei has a fibroblastic origin different to the classical somitic origin, highlighting a cellular heterogeneity of myonuclei in foetal myotubes. To gain insights on the functional relevance of myonucleus heterogeneity during limb development, we used 2D culture and co-culture systems to dissociate autonomous processes (occurring in 2D-cultures) from 3D-environment of tissue development. We also assessed the role of muscle contraction in myonucleus heterogeneity in paralysed limb muscles. The regionalisation of cellular heterogeneity was not observed in 2D cell culture systems and paralyzed muscles. The molecular signature of MTJ myonuclei was lost in a dish and paralysed muscles indicating a requirement of 3D-enviroment and muscle contraction for MTJ formation. Tip genes that maintain a regionalized expression at myotube tips in cultures are linked to sarcomeres. The behaviour of regionalized markers in cultured myotubes and paralyzed muscles allows us to speculate whether the genes intervene in myogenesis, myotube attachment or MTJ formation.

三维环境和肌肉收缩调节肌核的异质性
骨骼肌的形成涉及肌肉细胞和相关结缔组织成纤维细胞之间的紧密相互作用。每块肌肉都显示出相同的组织类型,它们在中部接受神经支配,在两端与肌腱相连。肌核沿着肌管呈异质分布,并根据这些中间和顶端区域进行区域化。在发育过程中,肌管一形成,面向发育中肌腱的肌尖上的肌核就会显示出自己的分子程序。除了分子异质性外,尖端肌核的一个子集还具有不同于传统体细胞起源的成纤维细胞起源,这凸显了胎儿肌管中肌核的细胞异质性。为了深入了解肌核异质性在肢体发育过程中的功能相关性,我们使用了二维培养和共培养系统,将(在二维培养中发生的)自主过程与组织发育的三维环境分离开来。我们还评估了肌肉收缩在瘫痪肢体肌肉肌核异质性中的作用。在二维细胞培养系统和瘫痪肌肉中均未观察到细胞异质性的区域化。MTJ肌核的分子特征在平皿和瘫痪肌肉中消失了,这表明MTJ的形成需要三维环境和肌肉收缩。在培养物中肌管尖端保持区域化表达的尖端基因与肌节有关。培养肌管和瘫痪肌肉中区域化标记的表现使我们能够推测这些基因是否参与了肌生成、肌管附着或 MTJ 的形成。
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来源期刊
Skeletal Muscle
Skeletal Muscle CELL BIOLOGY-
CiteScore
9.10
自引率
0.00%
发文量
25
审稿时长
12 weeks
期刊介绍: The only open access journal in its field, Skeletal Muscle publishes novel, cutting-edge research and technological advancements that investigate the molecular mechanisms underlying the biology of skeletal muscle. Reflecting the breadth of research in this area, the journal welcomes manuscripts about the development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration of skeletal muscle, with an emphasis on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators. Main areas of interest include: -differentiation of skeletal muscle- atrophy and hypertrophy of skeletal muscle- aging of skeletal muscle- regeneration and degeneration of skeletal muscle- biology of satellite and satellite-like cells- dystrophic degeneration of skeletal muscle- energy and glucose homeostasis in skeletal muscle- non-dystrophic genetic diseases of skeletal muscle, such as Spinal Muscular Atrophy and myopathies- maintenance of neuromuscular junctions- roles of ryanodine receptors and calcium signaling in skeletal muscle- roles of nuclear receptors in skeletal muscle- roles of GPCRs and GPCR signaling in skeletal muscle- other relevant aspects of skeletal muscle biology. In addition, articles on translational clinical studies that address molecular and cellular mechanisms of skeletal muscle will be published. Case reports are also encouraged for submission. Skeletal Muscle reflects the breadth of research on skeletal muscle and bridges gaps between diverse areas of science for example cardiac cell biology and neurobiology, which share common features with respect to cell differentiation, excitatory membranes, cell-cell communication, and maintenance. Suitable articles are model and mechanism-driven, and apply statistical principles where appropriate; purely descriptive studies are of lesser interest.
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