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Lactoferrin promotes murine C2C12 myoblast proliferation and differentiation and myotube hypertrophy

机译:乳铁蛋白促进小鼠C2C12成肌细胞增殖和分化以及肌管肥大

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摘要

Lactoferrin (Lf) is a multifunctional glycoprotein, which promotes the proliferation of murine C2C12 myoblasts. In the present study, it was investigated how Lf promotes myoblast proliferation and whether Lf promotes myoblast differentiation or induces myotube hypertrophy. Lf promoted the proliferation of myoblasts in a dose-dependent manner. Myoblast proliferation increased on day 3 when myoblasts were cultured in the presence of Lf for three days and also when myoblasts were cultured in the presence of Lf for the first day and in the absence of Lf for the subsequent two days. In addition, Lf induced the phosphorylation of extracellular signal-regulated kinase (ERK)1/2 in myoblasts. The mitogen-activated protein kinase kinase 1/2 inhibitor U0126 inhibited Lf-induced ERK1/2 phosphorylation and repressed Lf-promoted myoblast proliferation. C2C12 myoblasts, myotubes and skeletal muscle expressed low-density lipoprotein receptor-related protein (LRP)1 mRNA and Lf-promoted myoblast proliferation was attenuated by an LRP1 antagonist or LRP1 gene silencing. The knockdown of LRP1 repressed Lf-induced phosphorylation of ERK1/2. Furthermore, when myoblasts were induced to differentiate, Lf increased the expression of the myotube-specific structural protein, myosin heavy chain (MyHC) and promoted myotube formation. Knockdown of LRP1 repressed Lf-induced MyHC expression. Lf also increased myotube size following differentiation. These results indicate that Lf promotes myoblast proliferation and differentiation, at least partially through LRP1 and also stimulates myotube hypertrophy.
机译:乳铁蛋白(Lf)是一种多功能糖蛋白,可促进鼠C2C12成肌细胞的增殖。在本研究中,研究了Lf如何促进成肌细胞增殖以及Lf是否促进成肌细胞分化或诱导肌管肥大。 Lf以剂量依赖性方式促进成肌细胞的增殖。当在Lf存在下培养成肌细胞三天时,以及在第一天在Lf存在下培养成肌细胞且随后两天不存在Lf的情况下培养成肌细胞时,第3天成肌细胞增殖增加。此外,Lf诱导成肌细胞中细胞外信号调节激酶(ERK)1/2的磷酸化。有丝分裂原激活的蛋白激酶激酶1/2抑制剂U0126抑制Lf诱导的ERK1 / 2磷酸化并抑制Lf促进的成肌细胞增殖。 C2C12成肌细胞,肌管和骨骼肌表达的低密度脂蛋白受体相关蛋白(LRP)1 mRNA和Lf促进的成肌细胞增殖被LRP1拮抗剂或LRP1基因沉默所减弱。 LRP1的组合式抑制Lf诱导的ERK1 / 2磷酸化。此外,当诱导成肌细胞分化时,Lf增加了肌管特异性结构蛋白,肌球蛋白重链(MyHC)的表达并促进了肌管的形成。敲低LRP1抑制Lf诱导的MyHC表达。分化后Lf也增加了肌管的大小。这些结果表明,Lf至少部分地通过LRP1促进成肌细胞的增殖和分化,并刺激肌管肥大。

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