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MGF Igf-1-ec

IGF-1Ec, IGF-1Eb, Mechano-Growth Factor

Quick Stats
Studies 62
Trials 100
Score 2
2024 pubmed

Mechano-growth factor regulates periodontal ligament stem cell proliferation and differentiation through Fyn-RhoA-YAP signaling.

Feng. Fan F; Tu. Teng T; Wang. Hui H; Song. Runfang R; Li. Junrong J; Zhu. Yue Y; Zhang. Songbai S; Zhang. Min M; Zhao. Ying Y; Liu. Yanli Y

Key Findings

  • MGF boosts proliferation and fibrogenic differentiation of periodontal ligament stem cells
  • MGF triggers phosphorylation of Fyn and YAP at Y357, but not LATS1‑YAP at S127
  • RhoA is required for Fyn‑mediated activation of YAP in response to MGF

Practical Outcomes

  • The findings hint that MGF might be useful for gum‑tissue repair, but they are limited to cell‑culture work. No dosage, delivery method, or safety data are provided, so biohackers would need more research before trying any protocols.

Summary

The study shows that a protein called Mechano‑Growth Factor (MGF) can make gum‑line stem cells grow and turn into tissue‑building cells by activating a specific chain of signals (Fyn‑RhoA‑YAP). This effect was seen in lab dishes, not in people, and it doesn’t involve the usual LATS1‑YAP route.

Abstract

Mechano-growth factor (MGF), which is a growth factor produced specifically in response to mechanical stimuli, with potential of tissue repair and regeneration. Our previous research has shown that MGF plays a crucial role in repair of damaged periodontal ligaments by promoting differentiation of periodontal ligament stem cells (PDLSCs). However, the molecular mechanism is not fully understood. This study aimed to investigated the regulatory effect of MGF on differentiation of PDLSCs and its molecular mechanism. Initially, we investigated how MGF impacts cell growth and differentiation, and the relationship with the activation of Fyn-p-YAP<sup>Y357</sup> and LATS1-p-YAP<sup>S127</sup>. Then, inhibitors were used to interfere Fyn phosphorylation to verify the role of Fyn-p-YAP <sup>Y357</sup> signal after MGF stimulation; moreover, siRNA was used to downregulate YAP expression to clarify the function of YAP in PDLSCs proliferation and differentiation. Finally, after C3 was used to inhibit the RhoA expression, we explored the role of RhoA in the Fyn-p-YAP <sup>Y357</sup> signaling pathway in PDLSCs proliferation and differentiation. Our study revealed that MGF plays a regulatory role in promoting PDLSCs proliferation and fibrogenic differentiation by inducing Fyn-YAP<sup>Y357</sup> phosphorylation but not LATS1-YAP <sup>S127</sup> phosphorylation. Moreover, the results indicated that Fyn could not activate YAP directly but rather activated YAP through RhoA in response to MGF stimulation. The research findings indicated that the Fyn-RhoA-p-YAP<sup>Y357</sup> pathway is significant in facilitating the proliferation and fibrogenic differentiation of PDLSCs by MGF. Providing new ideas for the study of MGF in promoting periodontal regenerative repair.

Study Information

Provider

pubmed

Year

2024

Date

2024-07-25T00:00:00.000Z

DOI

10.1016/j.bbrc.2024.150450

References

47