MedicalResearch.com Interview with:
[caption id="attachment_34984" align="alignleft" width="200"]
Dr. Jean-François Cailhier[/caption]
Jean-François Cailhier, M.D., Ph.D., FRCP(c)
Professeur Agrégé de Clinique/ Associate Professor
Département de Médecine, Faculté de Médecine
Université de Montreal
MedicalResearch.com: What is the background for this study? What are the main findings?
Response: Milk Fat Globule Epidermal Growth Factor-8 (MFG-E8) is released by apoptotic cells and activated cells in the skin. Its effect on endothelial cells and pericytes was previously reported to accelerate wound healing.
In our wound healing model, we demonstrated that MFG-E8 was important to reprogram skin macrophages into pro-repair cells. Moreover, we demonstrated that administration of exogenous MFG-E8 was able to accelerate wound healing in WT and MFG-E8 KO mice by generating M2 macrophages. Furthermore, to highlight to importance of MFG-E8 on macrophage reprogramming, adoptive transfer of MFG-E8-treated macrophages also promoted wound healing. These pro-repair effects seem to be dependent on the production of a crucial fibroblast growth factor, basic Fibroblast Growth Factor (bFGF), by macrophages which promoted fibroblast migration and proliferation.
Dr. Jean-François Cailhier[/caption]
Jean-François Cailhier, M.D., Ph.D., FRCP(c)
Professeur Agrégé de Clinique/ Associate Professor
Département de Médecine, Faculté de Médecine
Université de Montreal
MedicalResearch.com: What is the background for this study? What are the main findings?
Response: Milk Fat Globule Epidermal Growth Factor-8 (MFG-E8) is released by apoptotic cells and activated cells in the skin. Its effect on endothelial cells and pericytes was previously reported to accelerate wound healing.
In our wound healing model, we demonstrated that MFG-E8 was important to reprogram skin macrophages into pro-repair cells. Moreover, we demonstrated that administration of exogenous MFG-E8 was able to accelerate wound healing in WT and MFG-E8 KO mice by generating M2 macrophages. Furthermore, to highlight to importance of MFG-E8 on macrophage reprogramming, adoptive transfer of MFG-E8-treated macrophages also promoted wound healing. These pro-repair effects seem to be dependent on the production of a crucial fibroblast growth factor, basic Fibroblast Growth Factor (bFGF), by macrophages which promoted fibroblast migration and proliferation.

















