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Titel: Nanofat Accelerates and Improves the Vascularization, Lymphatic Drainage and Healing of Full-Thickness Murine Skin Wounds
VerfasserIn: Limido, Ettore
Weinzierl, Andrea
Ampofo, Emmanuel
Harder, Yves
Menger, Michael D.
Laschke, Matthias W.
Sprache: Englisch
Titel: International Journal of Molecular Sciences
Bandnummer: 25
Heft: 2
Verlag/Plattform: MDPI
Erscheinungsjahr: 2024
Freie Schlagwörter: wound healing
nanofat
platelet-rich plasma
vascularization
angiogenesis
lymph vessels
macrophages
DDC-Sachgruppe: 610 Medizin, Gesundheit
Dokumenttyp: Journalartikel / Zeitschriftenartikel
Abstract: The treatment of wounds using the body’s own resources is a promising approach to support the physiological regenerative process. To advance this concept, we evaluated the effect of nanofat (NF) on wound healing. For this purpose, full-thickness skin defects were created in dorsal skinfold chambers of wild-type mice. These defects were filled with NF generated from the inguinal subcutaneous adipose tissue of green fluorescent protein (GFP)+ donor mice, which was stabilized using platelet-rich plasma (PRP). Empty wounds and wounds solely filled with PRP served as controls. Wound closure, vascularization and formation of granulation tissue were repeatedly analyzed using stereomicroscopy, intravital fluorescence microscopy, histology and immunohistochemistry over an observation period of 14 days. PRP + NF-treated wounds exhibited accelerated vascularization and wound closure when compared to controls. This was primarily due to the fact that the grafted NF contained a substantial fraction of viable GFP+ vascular and lymph vessel fragments, which interconnected with the GFP− vessels of the host tissue. Moreover, the switch from inflammatory M1- to regenerative M2-polarized macrophages was promoted in PRP + NF-treated wounds. These findings indicate that NF markedly accelerates and improves the wound healing process and, thus, represents a promising autologous product for future wound management.
DOI der Erstveröffentlichung: 10.3390/ijms25020851
URL der Erstveröffentlichung: https://doi.org/10.3390/ijms25020851
Link zu diesem Datensatz: urn:nbn:de:bsz:291--ds-415089
hdl:20.500.11880/37193
http://dx.doi.org/10.22028/D291-41508
ISSN: 1422-0067
Datum des Eintrags: 29-Jan-2024
Fakultät: M - Medizinische Fakultät
Fachrichtung: M - Chirurgie
Professur: M - Prof. Dr. Michael D. Menger
Sammlung:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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