MGF E peptide pretreatment improves collagen synthesis and cell proliferation of injured human ACL fibroblasts via MEK-ERK1/2 signaling pathway.
Sha. Yongqiang Y; Afandi. Ruli R; Zhang. Bingbing B; Yang. Li L; Lv. Yonggang Y
Key Findings
- MGF‑E peptide reduced early type I/III collagen production but boosted type III collagen after 24 h
- It lowered MMP‑2 activity, which normally degrades matrix proteins
- It accelerated fibroblast proliferation via the MEK‑ERK1/2 signaling pathway
Practical Outcomes
- The results suggest MGF‑E could be explored as a supplement or injection to aid ligament healing, but the study is only in cell cultures. No human dosing or safety data exist yet, so biohackers should treat this as early‑stage evidence and await animal or clinical trials before applying it.
Summary
A lab study found that treating injured knee ligament cells with the MGF‑E peptide helped them grow faster and make more of the right kind of collagen, while also lowering enzymes that break down tissue. This effect works through a known cell‑signaling pathway (MEK‑ERK1/2).
Abstract
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.
Study Information
pubmed
2017
2017-05-29T00:00:00.000Z
10.1080/08977194.2017.1327856
13
41