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胎牛骨髓间充质干细胞的成肌分化潜能

Myogenic Differentiation Potential of Mesenchymal Stem Cells Derived from Fetal Bovine Bone Marrow.

作者信息

Okamura Lucas Hidenori, Cordero Paloma, Palomino Jaime, Parraguez Victor Hugo, Torres Cristian Gabriel, Peralta Oscar Alejandro

机构信息

a Departamento de Apoio, Produção e Saúde Animal, Faculdade de Medicina Veterinária , Universidade Estadual Paulista "Júlio de Mesquita Filho" , Araçatuba , São Paulo , Brasil.

b Departamento de Fomento de la Producción Animal, Facultad de Ciencias Veterinarias y Pecuarias , Universidad de Chile , Santiago , Chile.

出版信息

Anim Biotechnol. 2018 Jan 2;29(1):1-11. doi: 10.1080/10495398.2016.1276926. Epub 2017 Mar 7.

Abstract

The myogenic potential of bovine fetal MSC (bfMSC) derived from bone marrow (BM) remains unknown; despite its potential application for the study of myogenesis and its implications for livestock production. In the present study, three protocols for in vitro myogenic differentiation of bfMSC based on the use of DNA methyltransferase inhibitor 5-Aza-2'-deoxycytidine (5-Aza), myoblast-secreted factor Galectin-1 (Gal-1), and myoblast culture medium SkGM-2 BulletKit were used. Plastic-adherent bfMSC were isolated from fetal BM collected from abattoir-derived fetuses. Post-thaw viability analyses detected 85.6% bfMSC negative for propidium iodine (PI). Levels of muscle regulatory factors (MRF) MYF5, MYF6, MYOD, and DES mRNA were higher (P < 0.05) in bfMSC cultured under 100 µM of 5-Aza compared to 1 and 10 µM. Treatment of bfMSC with 10 µM of 5-Aza resulted in down-regulation of MYOD mRNA (Days 7 to 21) and up-regulation of MYF6 (Day 7), MYF5, and DES mRNA (Day 21). Gal-1 and SkGM-2 BulletKit induced sequential down-regulation of early MRF (MYF5) and up-regulation of intermediate (MYOD) and late MRF (DES) mRNA. Moreover, DES and MYF5 were immunodetected in differentiated bfMSC. In conclusion, protocols evaluated in bfMSC induced progress into myogenic differentiation until certain extent evidenced by changes in MRF gene expression.

摘要

源自骨髓(BM)的牛胎儿间充质干细胞(bfMSC)的生肌潜力仍然未知;尽管其在肌发生研究及其对畜牧生产的影响方面具有潜在应用价值。在本研究中,使用了三种基于DNA甲基转移酶抑制剂5-氮杂-2'-脱氧胞苷(5-Aza)、成肌细胞分泌因子半乳糖凝集素-1(Gal-1)以及成肌细胞培养基SkGM-2 BulletKit的bfMSC体外成肌分化方案。从屠宰场来源的胎儿收集的胎儿骨髓中分离出贴壁生长的bfMSC。解冻后活力分析检测到85.6%的bfMSC对碘化丙啶(PI)呈阴性。与1μM和10μM相比,在100μM 5-Aza培养条件下的bfMSC中,肌肉调节因子(MRF)MYF5、MYF6、MYOD和DES mRNA的水平更高(P < 0.05)。用10μM 5-Aza处理bfMSC导致MYOD mRNA下调(第7至21天)以及MYF6(第7天)、MYF5和DES mRNA上调(第21天)。Gal-1和SkGM-2 BulletKit诱导早期MRF(MYF5)的顺序下调以及中期(MYOD)和晚期MRF(DES)mRNA的上调。此外,在分化的bfMSC中免疫检测到了DES和MYF5。总之,在bfMSC中评估的方案诱导其向成肌分化进展,直至一定程度,这通过MRF基因表达的变化得以证明。

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