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      Histological and Immunohistochemical Analyses of Repair of the Disc in the Rabbit Temporomandibular Joint Using a Collagen Template

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          Abstract

          A previous study demonstrated that the reconstituted type I collagen matrix extracted from rabbit tendons enabled the TMJ disc to regenerate in the rabbit. The aim of this study was to investigate changes in the extracellular matrix (ECM) and mechanisms of regeneration in the TMJ disc. In 36 New Zealand rabbits that underwent a partial discectomy, discs were replaced with reconstituted collagen templates for 3 months. A histological analysis showed that moderate to severe degeneration appeared in partially discectomized joints without implantation. In contrast, discs experienced regeneration of reconstituted collagen template implantation and the joint returned to normal function. Cells in the regenerative tissue expressed ECM, and fibers became regular and compact due to tissue remodeling over time. Reparative cells differentiated into chondroblasts, and showed highly dense pericellular fibers. The morphology and collagen composition of the disc and condyle in the 3-month experimental group were similar to those of normal tissues. In conclusion, the reconstituted collagen template facilitated the regeneration of surgically discectomized discs. Type I and type II collagens play a crucial role in the regeneration of articular discs.

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          Most cited references36

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          Temporomandibular disorders.

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            The bladder extracellular matrix. Part I: architecture, development and disease.

            From the earliest studies with epithelial cells implanted into detrusor muscle to later experiments on smooth muscle in defined collagen gels, cell niche and extracellular matrix (ECM) have been clearly shown to orchestrate cellular behavior and fate whether quiescent, migratory, or proliferative. Normal matrix can revert transformed cells to quiescence, and damaged matrix can trigger malignancy or dedifferentiation. ECM influence in disease, development, healing and regeneration has been demonstrated in many other fields of study, but a thorough examination of the roles of ECM in bladder cell activity has not yet been undertaken. Structural ECM proteins, in concert with adhesive proteins, provide crucial structural support to the bladder. Both structural and nonstructural components of the bladder have major effects on smooth muscle function, through effects on matrix rigidity and signaling through ECM receptors. While many ECM components and receptors identified in the bladder have specific known functions in the vascular smooth musculature, their function in the bladder is often less well defined. In cancer and obstructive disease, the ECM has a critical role in pathogenesis. The challenge in these settings will be to find therapies that prevent hyperproliferation and encourage proper differentiation, through an understanding of matrix effects on cell biology and susceptibility to therapeutics.
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              Structure of a collagen-GAG dermal skin substitute optimized for cultured human epidermal keratinocytes.

              Collagen and glycosaminoglycan (GAG) dermal skin substitutes (membranes) were studied as substrates for cultured human epidermal keratinocytes. Structure of dermal substitutes was optimized for pore size to promote ingrowth of fibrovascular tissue from the wound bed and for culture of human keratinocytes of the membrane's surface. Pore size of the freeze-dried material was regulated by control of the temperature of freezing between -50 degrees C and -20 degrees C and by concentration of starting materials between 0.17% and 1.62% wt/vol. A nonporous surface of collagen-GAG was laminated to the membranes to provide a planar substrate for cultured epidermal keratinocytes. Thickness of dermal substitutes was regulated by control of the volume and concentration of starting materials. Biotin was conjugated to solubilized collagen for binding with avidin of specific quantities of biologically active molecules. The optimized membranes are suitable substrates for the culture of human epidermal keratinocytes, and together with the cells yield a composite material that is histologically similar to skin.
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                Author and article information

                Journal
                Materials (Basel)
                Materials (Basel)
                materials
                Materials
                MDPI
                1996-1944
                09 August 2017
                August 2017
                : 10
                : 8
                : 924
                Affiliations
                [1 ]Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan; khwang117@ 123456gmail.com (K.-H.W.); dryangcb@ 123456gmail.com (C.-B.Y.); kuanchou@ 123456tmu.edu.tw (K.-C.C.)
                [2 ]Department of Radiology, School of Medicine, College of Medicine, Taipei Medical Univesity, Taipei 110, Taiwan; wp.chan@ 123456msa.hinet.net
                [3 ]McLean Imaging Center, Harvard Medical School, Belmont, MA 02478, USA; lchiu@ 123456mclean.harvard.edu
                [4 ]Graduate Institute of Medical Sciences, Taipei Medical University, Taipei 11031, Taiwan; cmbyht18@ 123456tmu.edu.tw (Y.-H.T.); d102094012@ 123456tmu.edu.tw (H.-L.T.)
                [5 ]Department of Pathology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan; ccllfang@ 123456tmu.edu.tw
                [6 ]School of Dentistry, College of Dentistry, Taipei Medical University, Taipei 11031, Taiwan
                Author notes
                [* ]Correspondence: laitw@ 123456tmu.edu.tw ; Tel.: +886-2-2391-6632
                [†]

                Co-first authors contributed equally to this article.

                [‡]

                Co-corresponding author.

                Author information
                https://orcid.org/0000-0001-8322-6336
                Article
                materials-10-00924
                10.3390/ma10080924
                5578290
                28792464
                4a334a98-04c7-47a7-8e85-c466fb559830
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 07 July 2017
                : 03 August 2017
                Categories
                Article

                temporomandibular joint disc,reconstituted collagen template,tissue regeneration

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