دوره 14، شماره 2 - ( 4-1405 )                   جلد 14 شماره 2 صفحات 42-38 | برگشت به فهرست نسخه ها


XML English Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Mohammadi S. Beyond osteogenesis and angiogenesis: The immunomodulatory role of macrophages in hAMSC-sEV-mediated repair of osteoradionecrosis of the jaw. , Jorjani Biomed J. 2026; 14 (2) :38-42
URL: http://goums.ac.ir/jorjanijournal/article-1-1138-fa.html
Beyond osteogenesis and angiogenesis: The immunomodulatory role of macrophages in hAMSC-sEV-mediated repair of osteoradionecrosis of the jaw. , فصلنامه علمی پژوهشی زیست پزشکی جرجانی. 1405; 14 (2) :38-42

URL: http://goums.ac.ir/jorjanijournal/article-1-1138-fa.html


چکیده:   (7682 مشاهده)
Osteoradionecrosis of the jaw (ORNJ) is a severe late complication of radiotherapy driven by vascular injury, hypoxia, fibrosis, persistent inflammation, and impaired bone remodeling. A recent study demonstrated that human amniotic mesenchymal stem cell-derived small extracellular vesicles (hAMSC-sEVs) improve ORNJ repair by restoring osteogenic differentiation of irradiated bone marrow mesenchymal stem cells through PI3K/AKT signaling and enhancing endothelial angiogenic activity through Wnt/β-catenin signaling. These findings establish an important regenerative framework but leave the immune compartment largely unexplored. We propose that macrophages represent a critical mechanistic link between hAMSC-sEV therapy and coordinated tissue repair. By reprogramming radiation-dysregulated macrophages toward pro-resolving, reparative phenotypes, hAMSC-sEVs may suppress chronic inflammation while simultaneously supporting osteogenesis and neovascularization. Defining the extracellular-vesicle cargo and macrophage signaling networks responsible for this effect could advance osteoimmunology-informed strategies and improve the translational development of cell-free therapies for ORNJ. This perspective highlights priorities for experimental validation and future clinical translation.
متن کامل [PDF 639 kb]   (1141 دریافت)    
سرمقاله: مرور کوتاه | موضوع مقاله: علوم مولکولی
دریافت: 1405/1/31 | پذیرش: 1405/3/9 | انتشار: 1405/4/4

ارسال نظر درباره این مقاله : نام کاربری یا پست الکترونیک شما:
CAPTCHA

بازنشر اطلاعات
این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به مجله زیست پزشکی جرجانی می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

© 2026 CC BY-NC 4.0 | Jorjani Biomedicine Journal

Designed & Developed by : Yektaweb