Attenuation of knee osteoarthritis progression in mice through polarization of m2 macrophages by intra-articular transplantation of non-cultured human adipose-derived regenerative cells

16Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

Adipose-derived regenerative cells (ADRCs) are non-cultured heterogeneous or mixed populations of cells obtained from adipose tissue by collagenase digestion. The injection of ADRCs have been tried clinically for the treatment of osteoarthritis (OA). The purpose of this study was to evaluate the effect of intra-articular transplantation of human ADRCs on OA progression in mice and the effect of ADRCs on macrophage polarization. In in vivo experiments, BALB/c-nu mice with knee OA received intra-articular transplantation of either phosphate buffered-saline or human ADRCs. OA progression was evaluated histologically and significantly attenuated in the ADRC group at both four and eight weeks postoperatively. The expression of OA-related proteins in the cartilage and macrophage-associated markers in the synovium were examined by immunohisto-chemistry. The numbers of MMP-13-, ADAMTS-5-, IL-1β-, IL-6-and iNOS-positive cells significantly decreased, and type II collagen-and CD206-positive cells were more frequently detected in the ADRC group compared with that in the control group. In vitro co-culture experiments showed that ADRCs induced macrophage polarization toward M2. The results of this study suggest that the intra-articular transplantation of human ADRCs could attenuate OA progression possibly by re-ducing catabolic factors in chondrocytes and modulating macrophage polarization.

Cite

CITATION STYLE

APA

Kamada, K., Matsushita, T., Yamashita, T., Matsumoto, T., Iwaguro, H., Sobajima, S., & Kuroda, R. (2021). Attenuation of knee osteoarthritis progression in mice through polarization of m2 macrophages by intra-articular transplantation of non-cultured human adipose-derived regenerative cells. Journal of Clinical Medicine, 10(19). https://doi.org/10.3390/jcm10194309

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free