119
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Exploiting endogenous fibrocartilage stem cells to regenerate cartilage and repair joint injury

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Tissue regeneration using stem cell-based transplantation faces many hurdles. Alternatively, therapeutically exploiting endogenous stem cells to regenerate injured or diseased tissue may circumvent these challenges. Here we show resident fibrocartilage stem cells (FCSCs) can be used to regenerate and repair cartilage. We identify FCSCs residing within the superficial zone niche in the temporomandibular joint (TMJ) condyle. A single FCSC spontaneously generates a cartilage anlage, remodels into bone and organizes a haematopoietic microenvironment. Wnt signals deplete the reservoir of FCSCs and cause cartilage degeneration. We also show that intra-articular treatment with the Wnt inhibitor sclerostin sustains the FCSC pool and regenerates cartilage in a TMJ injury model. We demonstrate the promise of exploiting resident FCSCs as a regenerative therapeutic strategy to substitute cell transplantation that could be beneficial for patients suffering from fibrocartilage injury and disease. These data prompt the examination of utilizing this strategy for other musculoskeletal tissues.

          Abstract

          A potentially superior tissue regenerative strategy to stem cell transplantation is modulation of endogenous stem cells. Here the authors show fibrocartilage stem cells exist in the temporomandibular joint that contribute to cartilage regeneration and can be manipulated to enhance regeneration through canonical Wnt signalling.

          Related collections

          Most cited references53

          • Record: found
          • Abstract: found
          • Article: not found

          Osteoarthritis cartilage histopathology: grading and staging.

          Current osteoarthritis (OA) histopathology assessment methods have difficulties in their utility for early disease, as well as their reproducibility and validity. Our objective was to devise a more useful method to assess OA histopathology that would have wide application for clinical and experimental OA assessment and would become recognized as the standard method. An OARSI Working Group deliberated on principles, standards and features for an OA cartilage pathology assessment system. Using current knowledge of the pathophysiology of OA morphologic features, a proposed system was presented at OARSI 2000. Subsequently, this was widely circulated for comments amongst experts in OA pathology. An OA cartilage pathology assessment system based on six grades, which reflect depth of the lesion and four stages reflecting extent of OA over the joint surface was developed. The OARSI cartilage OA histopathology grading system appears consistent and simple to apply. Further studies are required to confirm the system's utility.
            • Record: found
            • Abstract: found
            • Article: not found

            WNT signaling in bone homeostasis and disease: from human mutations to treatments.

            Low bone mass and strength lead to fragility fractures, for example, in elderly individuals affected by osteoporosis or children with osteogenesis imperfecta. A decade ago, rare human mutations affecting bone negatively (osteoporosis-pseudoglioma syndrome) or positively (high-bone mass phenotype, sclerosteosis and Van Buchem disease) have been identified and found to all reside in components of the canonical WNT signaling machinery. Mouse genetics confirmed the importance of canonical Wnt signaling in the regulation of bone homeostasis, with activation of the pathway leading to increased, and inhibition leading to decreased, bone mass and strength. The importance of WNT signaling for bone has also been highlighted since then in the general population in numerous genome-wide association studies. The pathway is now the target for therapeutic intervention to restore bone strength in millions of patients at risk for fracture. This paper reviews our current understanding of the mechanisms by which WNT signalng regulates bone homeostasis.
              • Record: found
              • Abstract: found
              • Article: not found

              Self-renewing osteoprogenitors in bone marrow sinusoids can organize a hematopoietic microenvironment.

              The identity of cells that establish the hematopoietic microenvironment (HME) in human bone marrow (BM), and of clonogenic skeletal progenitors found in BM stroma, has long remained elusive. We show that MCAM/CD146-expressing, subendothelial cells in human BM stroma are capable of transferring, upon transplantation, the HME to heterotopic sites, coincident with the establishment of identical subendothelial cells within a miniature bone organ. Establishment of subendothelial stromal cells in developing heterotopic BM in vivo occurs via specific, dynamic interactions with developing sinusoids. Subendothelial stromal cells residing on the sinusoidal wall are major producers of Angiopoietin-1 (a pivotal molecule of the HSC "niche" involved in vascular remodeling). Our data reveal the functional relationships between establishment of the HME in vivo, establishment of skeletal progenitors in BM sinusoids, and angiogenesis.

                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group
                2041-1723
                10 October 2016
                2016
                : 7
                : 13073
                Affiliations
                [1 ]TMJ Biology and Regenerative Medicine Laboratory, College of Dental Medicine, Columbia University Medical Center , 630 W 168th St, P&S 16-440, New York, New York 10032, USA
                [2 ]Center for Craniofacial Regeneration, College of Dental Medicine, Columbia University Medical Center , 622 W 168th St, New York, New York 10032, USA
                [3 ]Department of Reconstructive Sciences, MC3705, L7005, University of Connecticut Health Sciences Center , 263 Farmington Avenue, Farmington, Connecticut 06032, USA
                [4 ]Clemson-MUSC Bioengineering Program, Department of Bioengineering, Clemson University , 173 Ashley Avenue, MSC 508, Charleston, South Carolina 29425, USA
                [5 ]Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences , 266 Fangzheng Avenue, Shuitu Hi-tech Industrial Park, Beibei District, Chongqing 400714, China
                [6 ]W.M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey , 604 Allison Road, D-251, Piscataway, New Jersey 08854, USA
                [7 ]Center for Musculoskeletal Research, University of Rochester Medical Center , 601 Elmwood Avenue, Box 665, Rochester, New York 14620, USA
                [8 ]Metropolitan Oral Surgery Associates, 488 Madison Avenue, #200 , New York, New York 10022, USA
                [9 ]College of Dental Medicine, Division of Oral and Maxillofacial Surgery, Columbia University Medical Center , 622 W 168th St, New York, New York 10032, USA
                Author notes
                Article
                ncomms13073
                10.1038/ncomms13073
                5062541
                27721375
                35031a42-90e4-4ea0-a980-f043592784ac
                Copyright © 2016, The Author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 11 January 2016
                : 01 September 2016
                Categories
                Article

                Uncategorized
                Uncategorized

                Comments

                Comment on this article

                Related Documents Log