Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
19
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Application of decellularized bone matrix as a bioscaffold in bone tissue engineering

      review-article

      Read this article at

      Bookmark
          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

          Autologous bone grafts are commonly used as the gold standard to repair and regenerate diseased bones. However, they are strongly associated with postoperative complications, especially at the donor site, and increased surgical costs. In an effort to overcome these limitations, tissue engineering (TE) has been proposed as an alternative to promote bone repair. The successful outcome of tissue engineering depends on the microstructure and composition of the materials used as scaffold. Decellularized bone matrix -based biomaterials have been applied as bioscaffolds in bone tissue engineering. These biomaterials play an important role in providing the mechanical and physical microenvironment needed by cells to proliferate and survive. Decellularized extracellular matrix (dECM) can be used as a powder, hydrogel and electrospun scaffolds. These bioscaffolds mimic the native microenvironment due to their structure similar to the original tissue. The aim of this review is to highlight the bone decellularization techniques. Herein we discuss: (1) bone structure; (2) properties of an ideal scaffold; (3) the potential of decellularized bone as bioscaffolds; (4) terminal sterilization of decellularized bone; (5) cell removing confirmation in decellularized tissues; and (6) post decellularization procedures. Finally, the improvement of bone formation by dECM and the immunogenicity aspect of using the decellularized bone matrix are presented, to illustrate how novel dECM-based materials can be used as bioscaffold in tissue engineering. A comprehensive understanding of tissue engineering may allow for better incorporation of therapeutic approaches in bone defects allowing for bone repair and regeneration.

          Related collections

          Most cited references110

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

          Signaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Tissue engineering

              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Osteoblast-Osteoclast Communication and Bone Homeostasis

              Bone remodeling is tightly regulated by a cross-talk between bone-forming osteoblasts and bone-resorbing osteoclasts. Osteoblasts and osteoclasts communicate with each other to regulate cellular behavior, survival and differentiation through direct cell-to-cell contact or through secretory proteins. A direct interaction between osteoblasts and osteoclasts allows bidirectional transduction of activation signals through EFNB2-EPHB4, FASL-FAS or SEMA3A-NRP1, regulating differentiation and survival of osteoblasts or osteoclasts. Alternatively, osteoblasts produce a range of different secretory molecules, including M-CSF, RANKL/OPG, WNT5A, and WNT16, that promote or suppress osteoclast differentiation and development. Osteoclasts also influence osteoblast formation and differentiation through secretion of soluble factors, including S1P, SEMA4D, CTHRC1 and C3. Here we review the current knowledge regarding membrane bound- and soluble factors governing cross-talk between osteoblasts and osteoclasts.
                Bookmark

                Author and article information

                Contributors
                f_amirazad@yahoo.com
                dadashpourm@semums.ac.ir
                zarghami@tbzmed.ac.ir
                Journal
                J Biol Eng
                J Biol Eng
                Journal of Biological Engineering
                BioMed Central (London )
                1754-1611
                5 January 2022
                5 January 2022
                2022
                : 16
                : 1
                Affiliations
                [1 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Department of Medical Biotechnology, Faculty of Advanced Medical Science, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                [2 ]GRID grid.486769.2, ISNI 0000 0004 0384 8779, Department of Biotechnology, Faculty of Medicine, , Semnan University of Medical Sciences, ; Semnan, Iran
                [3 ]GRID grid.486769.2, ISNI 0000 0004 0384 8779, Biotechnology Research Center, , Semnan University of Medical Sciences, ; Semnan, Iran
                [4 ]GRID grid.449300.a, ISNI 0000 0004 0403 6369, Deparment of Medical Biochemistry, Faculty of Medicine, , Istanbul Aydin Universioty, ; Istanbul, Turkey
                [5 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Department of Clinical Biochemistry and Laboratory Medicine, Faculty of Medicine, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                Author information
                https://orcid.org/0000-0003-0719-4357
                https://orcid.org/0000-0003-3352-7880
                https://orcid.org/0000-0002-4236-4537
                Article
                282
                10.1186/s13036-021-00282-5
                8734306
                34986859
                93b317ba-075e-4424-9c79-e59554abaabb
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 1 September 2021
                : 2 December 2021
                Funding
                Funded by: Tabriz University of Medical Sciences
                Award ID: 5/D/65618
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2022

                Biotechnology
                decellularized extracellular matrix,bioscaffold,tissue engineering,bone regeneration

                Comments

                Comment on this article