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

Author:

Borrelli Mimi R.1,Patel Ronak A.1,Adem Sandeep1,Diaz Deleon Nestor M.1,Shen Abra H.1,Sokol Jan1,Yen Sara1,Chang Erin Y.2,Nazerali Rahim1,Nguyen Dung1,Momeni Arash1,Wang Kevin C.2,Longaker Michael T.13,Wan Derrick C.1

Affiliation:

1. Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, Division of Plastic Surgery Stanford University School of Medicine, Stanford, California, USA

2. Program in Epithelial Biology, Department of Dermatology Stanford University School of Medicine, Stanford, California, USA

3. Stanford Institute for Stem Cell Biology and Regenerative Medicine Stanford University School of Medicine, Stanford, California, USA

Abstract

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.

Funder

PSF/MTF Biologics Allograft Tissue Research Grant

Stinehart-Reed Fund

Gunn/Olivier Research Fund

NIH

Sarnoff Cardiovascular Foundation

California Institute for Regenerative Medicine

Plastic Surgery Research Foundation

NIH S10 Shared Instrumentation Grant

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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