Poult Sci. 2017 Jun 1;96(6):1910-1917. doi: 10.3382/ps/pew434.
Myogenic satellite cells are an adult stem cell responsible for all post-hatch muscle growth in poultry. As a stem cell population, satellite cells are highly heterogeneous, but the origin of this heterogeneity remains unclear. Heterogeneity is, in part, regulated by gene expression. One method of endogenous gene regulation that may contribute to heterogeneity is microRNAs (miRNAs). Two miRNAs previously shown to regulate poultry myogenic satellite cell proliferation and differentiation, miR-128 and miR-24, were studied to determine if they also affected satellite cell migration. Satellite cell migration is an essential step for both proliferation and differentiation. During proliferation, satellite cells will migrate and align to form new myofibers or donate their nuclei to existing myofibers leading to muscle fiber hypertrophy or regeneration. Transient transfection of miRNA specific mimics to each miRNA reduced migration of satellite cells following a cell culture scratch at 72 h of proliferation when the cultures were 90 to 100% confluent. However, only the migration in cells transfected with miR-24 mimics at 24 and 30 h following the scratch was significantly reduced (P ≤ 0.05) to around 70% of the distance migrated by controls. Alternately, transfection with inhibitors specific to miR-128 or miR-24 significantly (P ≤ 0.05) increased migration between 147 and 252% compared to their controls between 24 and 48 h following the scratch. These data demonstrate that miR-128 and miR-24 play a role in myogenic satellite cell migration, which will impact muscle development and growth.
成肌卫星细胞是一种成体干细胞,负责禽类孵化后所有的肌肉生长。作为一种干细胞群体,卫星细胞具有高度异质性,但这种异质性的起源尚不清楚。异质性部分受基因表达调控。一种可能导致异质性的内源性基因调控方法是 microRNAs(miRNAs)。先前已经证明,miR-128 和 miR-24 这两种 miRNA 可以调节禽类成肌卫星细胞的增殖和分化,研究它们是否也影响卫星细胞的迁移。卫星细胞的迁移是增殖和分化的必要步骤。在增殖过程中,卫星细胞会迁移并排列以形成新的肌纤维,或者将其细胞核捐赠给现有的肌纤维,从而导致肌肉纤维肥大或再生。在增殖的 72 小时,当培养物达到 90%到 100%融合时,用 miRNA 特异性模拟物瞬时转染每种 miRNA 会减少卫星细胞的迁移。然而,只有在划痕后 24 和 30 小时转染 miR-24 模拟物的细胞的迁移显著减少(P≤0.05),约为对照细胞迁移距离的 70%。相反,转染 miR-128 或 miR-24 的抑制剂特异性转染在划痕后 24 到 48 小时之间显著(P≤0.05)增加了 147%到 252%的迁移,与对照相比。这些数据表明,miR-128 和 miR-24 参与了成肌卫星细胞的迁移,这将影响肌肉的发育和生长。