MGF E peptide pretreatment improves collagen synthesis and cell proliferation of injured human ACL fibroblasts via MEK-ERK1/2 signaling pathway

被引:16
|
作者
Sha, Yongqiang [1 ,2 ]
Afandi, Ruli [1 ,2 ]
Zhang, Bingbing [1 ,2 ]
Yang, Li [1 ,2 ]
Lv, Yonggang [1 ,2 ]
机构
[1] Chongqing Univ, Bioengn Coll, Key Lab Biorheol Sci & Technol, Minist Educ, Chongqing, Peoples R China
[2] Chongqing Univ, Bioengn Coll, Mechanobiol & Regenerat Med Lab, 174 Shazheng St, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Anterior cruciate ligament; mechano-growth factor; cell viability; collagen synthesis; injurious stretch; ANTERIOR CRUCIATE LIGAMENT; MECHANO-GROWTH-FACTOR; DIFFERENTIAL HEALING CAPACITY; MEDIAL COLLATERAL LIGAMENT; MESENCHYMAL STEM-CELLS; GENE-EXPRESSION; IN-VITRO; MIGRATION; CARTILAGE; DAMAGE;
D O I
10.1080/08977194.2017.1327856
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Injured anterior cruciate ligament (ACL) is hard to heal due to the poor proliferative potential of ACL fibroblasts. To verify whether mechano-growth factor (MGF) E peptide can restore the cell proliferation of injured ACL fibroblasts, ACL fibroblasts pretreated with MGF E peptide were subjected to injurious stretch and the outcomes were evaluated at 0 and 24 h. After injured, the type III collagen synthesis was increased at 0 h while inhibited at 24 h. The matrix metalloproteinase-2 (MMP-2) activity/expression was up-regulated, but the cell proliferation was inhibited. Fortunately, exogenous MGF E peptide decreased the type I/III collagen synthesis at 0 h but improved the type III collagen synthesis at 24 h. It decreased the MMP-2 activity/expression of injured ACL fibroblasts. Besides, MGF E peptide accelerated the cell proliferation via MEK-ERK1/2 signaling pathway. Our results implied that MGF E peptide pretreatment could provide a new efficient approach for ACL regeneration.
引用
收藏
页码:29 / 38
页数:10
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