Mesenchymal Stem Cells Reduce Intervertebral Disc Fibrosis and Facilitate Repair

Author:

Leung Victor Y.L.123,Aladin Darwesh M.K.14,Lv Fengjuan1,Tam Vivian1,Sun Yi1,Lau Roy Y.C.1,Hung Siu-Chun1,Ngan Alfonso H.W.5,Tang Bin6,Lim Chwee Teck478,Wu Ed X.9,Luk Keith D.K.1,Lu William W.1,Masuda Koichi10,Chan Danny23,Cheung Kenneth M.C.13

Affiliation:

1. Department of Orthopaedics & Traumatology The University of Hong Kong, Hong Kong SAR, People's Republic of China

2. Department of Biochemistry The University of Hong Kong, Hong Kong SAR, People's Republic of China

3. Centre for Reproduction, Development, and Growth The University of Hong Kong, Hong Kong SAR, People's Republic of China

4. Mechanobiology Institute National University of Singapore, Singapore

5. Department of Mechanical Engineering The University of Hong Kong, Hong Kong SAR, People's Republic of China

6. Department of Micro-nano Materials and Devices South University of Science and Technology of China, Guangzhou, People's Republic of China

7. Department of Bioengineering National University of Singapore, Singapore

8. Department of Mechanical Engineering National University of Singapore, Singapore

9. Department of Electrical & Electronic Engineering The University of Hong Kong, Hong Kong SAR, People's Republic of China

10. Department of Orthopaedic Surgery University of California, San Diego, California, USA

Abstract

Abstract Intervertebral disc degeneration is associated with back pain and radiculopathy which, being a leading cause of disability, seriously affects the quality of life and presents a hefty burden to society. There is no effective intervention for the disease and the etiology remains unclear. Here, we show that disc degeneration exhibits features of fibrosis in humans and confirmed this in a puncture-induced disc degeneration (PDD) model in rabbit. Implantation of bone marrow-derived mesenchymal stem cells (MSCs) to PDD discs can inhibit fibrosis in the nucleus pulposus with effective preservation of mechanical properties and overall spinal function. We showed that the presence of MSCs can suppress abnormal deposition of collagen I in the nucleus pulposus, modulating profibrotic mediators MMP12 and HSP47, thus reducing collagen aggregation and maintaining proper fibrillar properties and function. As collagen fibrils can regulate progenitor cell activities, our finding provides new insight to the limited self-repair capability of the intervertebral disc and importantly the mechanism by which MSCs may potentiate tissue regeneration through regulating collagen fibrillogenesis in the context of fibrotic diseases. Stem Cells  2014;32:2164–2177

Funder

Area of Excellence

General Research Fund

Research Grant Council of Hong Kong

HKU Foundation Seed Grant

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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