Vasculogenic potential of adipose tissue derived stem cells from patients with chronic spinal cord injury and pressure injuries

Identificadores
URI: http://hdl.handle.net/10498/39039
DOI: https://doi.org/10.1007/s10456-025-10002-y
ISSN: 1573-7209
ISSN: 0969-6970
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Santos de la Mata, Ángela; Esteban, Pedro F.; Martínez Torija, Mario; Paniagua Torija, Beatriz; Espino-Rodríguez, Francisco Javier; Beltrán Camacho, Lucía
; Camacho Toledano, Celia; Alcobendas Maestro, Mónica; García García, Fernando; Molina Holgado, Eduardo; Durán Ruiz, María del Carmen
; Melero Martin, Juan M.; Moreno Luna, Rafael
Date
2025-09-10Department
Biomedicina, Biotecnología y Salud PúblicaSource
Angiogenesis - 2025, Vol. 28 n.4Abstract
Limited vascularization and ischemia are major contributors to the chronicity of wounds, such as ulcers and traumatic
injuries, which impose significant medical, social, and economic burdens. These challenges are particularly pronounced in
patients with spinal cord injury (SCI), a disabling condition associated with vascular dysfunction, infections, and impaired
peripheral circulation, complicating the treatment of pressure injuries (PIs) and the success of reconstructive procedures
like grafts and flaps. Regenerative medicine aims to address these issues by identifying effective cellular therapies to
restore vascular beds. Among these, cells from the stromal vascular fraction (SVF) of adipose tissue (AT) are promising
due to their abundance of angiogenic and vasculogenic cells, including mesenchymal stem cells (MSCs) and endothelial
colony-forming cells (ECFCs). This study evaluated the vasculogenic potential of AT-derived cellular fractions isolated via
enzymatic digestion of white adipose tissue (WAT). We compared adipose-derived stem cells (ASCs) cultured from SVF
with a combination of ECFCs and MSCs, expanded separately and transplanted in a 40:60 ratio. Results showed that while
ASCs promote angiogenesis and vasculogenesis, the ECFC/MSC combination is superior, consistently forming perfused
vascular beds in subcutaneous implants in nude mice. Furthermore, ECFCs and MSCs extracted from small amounts of
WAT in SCI patients with PIs demonstrated similar functionality and vasculogenic potential to cells from healthy controls.
These findings highlight the potential of AT-derived ECFCs and MSCs in autologous cell therapies, offering a promising
avenue for advancing vascular regeneration in patients with SCI.
Subjects
Spinal cord injury; Pressure injury; Adipose tissue; Angiogenesis; Vasculogenesis; ASCs; MSCs; ECFCsCollections
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