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Taking cues from the extracellular matrix to design bone-mimetic regenerative scaffolds
Institution:1. Department of Biomedical Engineering, University of Alabama at Birmingham, 1918 University Boulevard, Birmingham, AL 35294, United States;2. Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, Birmingham, AL 35294, United States;1. State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China;2. Department of Prosthodontics, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China;3. State Key Laboratory of Polymer Materials Engineering Poly Research Institute of Sichuan University, Chengdu 610065, PR China;4. Department of Stomatology of People''s Liberation Army General Hospital, Beijing 100853, PR China;1. Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil;2. Laboratório de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia 74605-220, Brazil;3. Faculdade de Odontologia, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil;4. Departamento de Física, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil
Abstract:There is an ongoing need for effective materials that can replace autologous bone grafts in the clinical treatment of bone injuries and deficiencies. In recent years, research efforts have shifted away from a focus on inert biomaterials to favor scaffolds that mimic the biochemistry and structure of the native bone extracellular matrix (ECM). The expectation is that such scaffolds will integrate with host tissue and actively promote osseous healing. To further enhance the osteoinductivity of bone graft substitutes, ECM-mimetic scaffolds are being engineered with a range of growth factors (GFs). The technologies used to generate GF-modified scaffolds are often inspired by natural processes that regulate the association between endogenous ECMs and GFs. The purpose of this review is to summarize research centered on the development of regenerative scaffolds that replicate the fundamental collagen-hydroxyapatite structure of native bone ECM, and the functionalization of these scaffolds with GFs that stimulate critical events in osteogenesis.
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