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Status: Bibliographieeintrag

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Verfasst von:Wu, Mengfan [VerfasserIn]   i
 Matar, Dany Y. [VerfasserIn]   i
 Yu, Zhen [VerfasserIn]   i
 Chen, Ziyu [VerfasserIn]   i
 Knoedler, Samuel [VerfasserIn]   i
 Ng, Brian [VerfasserIn]   i
 Darwish, Oliver A. [VerfasserIn]   i
 Sohrabi, Sadaf [VerfasserIn]   i
 Friedman, Leigh [VerfasserIn]   i
 Haug, Valentin [VerfasserIn]   i
 Murphy, George F. [VerfasserIn]   i
 Rinkevich, Yuval [VerfasserIn]   i
 Orgill, Dennis P. [VerfasserIn]   i
 Panayi, Adriana C. [VerfasserIn]   i
Titel:Continuous NPWT regulates fibrosis in murine diabetic wound healing
Verf.angabe:Mengfan Wu, Dany Y. Matar, Zhen Yu, Ziyu Chen, Samuel Knoedler, Brian Ng, Oliver A. Darwish, Sadaf Sohrabi, Leigh Friedman, Valentin Haug, George F. Murphy, Yuval Rinkevich, Dennis P. Orgill and Adriana C. Panayi
E-Jahr:2022
Jahr:6 October 2022
Umfang:15 S.
Fussnoten:Gesehen am 18.01.2023
Titel Quelle:Enthalten in: Pharmaceutics
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2022
Band/Heft Quelle:14(2022), 10 vom: Okt., Artikel-ID 2125, Seite 1-15
ISSN Quelle:1999-4923
Abstract:Scarring is associated with significant morbidity. The mechanical signaling factor yes-associated protein (YAP) has been linked to Engrailed-1 (En1)-lineage positive fibroblasts (EPFs), a pro-scarring fibroblast lineage, establishing a connection between mechanotransduction and fibrosis. In this study, we investigate the impact of micromechanical forces exerted through negative pressure wound therapy (NPWT) on the pathophysiology of fibrosis. Full-thickness excisional dorsal skin wounds were created on diabetic (db/db) mice which were treated with occlusive covering (control) or NPWT (continuous, −125 mmHg, 7 days; NPWT). Analysis was performed on tissue harvested 10 days after wounding. NPWT was associated with increased YAP (p = 0.04) but decreased En1 (p = 0.0001) and CD26 (p < 0.0001). The pro-fibrotic factors Vimentin (p = 0.04), α-SMA (p = 0.04) and HSP47 (p = 0.0008) were decreased with NPWT. Fibronectin was higher (p = 0.01) and collagen deposition lower in the NPWT group (p = 0.02). NPWT increased cellular proliferation (p = 0.002) and decreased apoptosis (p = 0.03). Western blotting demonstrated increased YAP (p = 0.02) and RhoA (p = 0.03) and decreased Caspase-3 (p = 0.03) with NPWT. NPWT uncouples YAP from EPF activation, through downregulation of Caspace-3, a pro-apoptotic factor linked to keloid formation. Mechanotransduction decreases multiple pro-fibrotic factors. Through this multifactorial process, NPWT significantly decreases fibrosis and offers promising potential as a mode to improve scar appearance.
DOI:doi:10.3390/pharmaceutics14102125
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.3390/pharmaceutics14102125
 Volltext: https://www.mdpi.com/1999-4923/14/10/2125
 DOI: https://doi.org/10.3390/pharmaceutics14102125
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:caspase3
 fibrosis
 mechanotransduction
 NPWT
 scarring
 tissue regeneration
 wound healing
 YAP
K10plus-PPN:1831436345
Verknüpfungen:→ Zeitschrift

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