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心脏咽中胚层起源于哺乳动物咽的骨骼肌和结缔组织。

Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx.

机构信息

Aix-Marseille Université, CNRS UMR 7288, IBDM, 13009 Marseille, France

CNR Institute of Genetics and Biophysics Adriano Buzzati-Traverso, Via Pietro Castellino 111, 80131 Naples, Italy.

出版信息

Development. 2020 Feb 3;147(3):dev185256. doi: 10.1242/dev.185256.

Abstract

Cardiopharyngeal mesoderm (CPM) gives rise to muscles of the head and heart. Using genetic lineage analysis in mice, we show that CPM develops into a broad range of pharyngeal structures and cell types encompassing musculoskeletal and connective tissues. We demonstrate that CPM contributes to medial pharyngeal skeletal and connective tissues associated with both branchiomeric and somite-derived neck muscles. CPM and neural crest cells (NCC) make complementary mediolateral contributions to pharyngeal structures, in a distribution established in the early embryo. We further show that biallelic expression of the CPM regulatory gene , haploinsufficient in 22q11.2 deletion syndrome patients, is required for the correct patterning of muscles with CPM-derived connective tissue. Our results suggest that CPM plays a patterning role during muscle development, similar to that of NCC during craniofacial myogenesis. The broad lineage contributions of CPM to pharyngeal structures provide new insights into congenital disorders and evolution of the mammalian pharynx.

摘要

心咽中胚层(CPM)产生头和心脏的肌肉。通过在小鼠中的遗传谱系分析,我们表明 CPM 发育成广泛的咽结构和细胞类型,包括骨骼肌和结缔组织。我们证明 CPM 有助于与分支和体节衍生的颈部肌肉相关的中咽骨骼和结缔组织。CPM 和神经嵴细胞(NCC)在胚胎早期建立的分布中,对咽结构进行互补的中侧贡献。我们进一步表明,CPM 调节基因的双等位基因表达,在 22q11.2 缺失综合征患者中为单倍不足,对于具有 CPM 衍生结缔组织的肌肉的正确模式形成是必需的。我们的结果表明,CPM 在肌肉发育过程中发挥模式形成作用,类似于 NCC 在颅面肌发生中的作用。CPM 对咽结构的广泛谱系贡献为哺乳动物咽的先天障碍和进化提供了新的见解。

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