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The antifibrotic adipose-derived stromal cell: Grafted fat enriched with CD74+ adipose-derived stromal cells reduces chronic radiation-induced skin fibrosis.

Authors :
Borrelli MR
Patel RA
Adem S
Diaz Deleon NM
Shen AH
Sokol J
Yen S
Chang EY
Nazerali R
Nguyen D
Momeni A
Wang KC
Longaker MT
Wan DC
Source :
Stem cells translational medicine [Stem Cells Transl Med] 2020 Nov; Vol. 9 (11), pp. 1401-1413. Date of Electronic Publication: 2020 Jun 20.
Publication Year :
2020

Abstract

Fat grafting can reduce radiation-induced fibrosis. Improved outcomes are found when fat grafts are enriched with adipose-derived stromal cells (ASCs), implicating ASCs as key drivers of soft tissue regeneration. We have identified a subpopulation of ASCs positive for CD74 with enhanced antifibrotic effects. Compared to CD74- and unsorted (US) ASCs, CD74+ ASCs have increased expression of hepatocyte growth factor, fibroblast growth factor 2, and transforming growth factor β3 (TGF-β3) and decreased levels of TGF-β1. Dermal fibroblasts incubated with conditioned media from CD74+ ASCs produced less collagen upon stimulation, compared to fibroblasts incubated with media from CD74- or US ASCs. Upon transplantation, fat grafts enriched with CD74+ ASCs reduced the stiffness, dermal thickness, and collagen content of overlying skin, and decreased the relative proportions of more fibrotic dermal fibroblasts. Improvements in several extracellular matrix components were also appreciated on immunofluorescent staining. Together these findings indicate CD74+ ASCs have antifibrotic qualities and may play an important role in future strategies to address fibrotic remodeling following radiation-induced fibrosis.<br /> (© 2020 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.)

Details

Language :
English
ISSN :
2157-6580
Volume :
9
Issue :
11
Database :
MEDLINE
Journal :
Stem cells translational medicine
Publication Type :
Academic Journal
Accession number :
32563212
Full Text :
https://doi.org/10.1002/sctm.19-0317