✦ LIBER ✦

Engineering bone-like tissuein vitro using human bone marrow stem cells and silk scaffolds

✍ Scribed by Meinel, Lorenz ;Karageorgiou, Vassilis ;Hofmann, Sandra ;Fajardo, Robert ;Snyder, Brian ;Li, Chunmei ;Zichner, Ludwig ;Langer, Robert ;Vunjak-Novakovic, Gordana ;Kaplan, David L.

Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 309 KB
Volume: 71A
Category: Article
ISSN: 0021-9304
DOI: 10.1002/jbm.a.30117

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✦ Synopsis

Abstract

Porous biodegradable silk scaffolds and human bone marrow derived mesenchymal stem cells (hMSCs) were used to engineer bone‐like tissue in vitro. Two different scaffolds with the same microstructure were studied: collagen (to assess the effects of fast degradation) and silk with covalently bound RGD sequences (to assess the effects of enhanced cell attachment and slow degradation). The hMSCs were isolated, expanded in culture, characterized with respect to the expression of surface markers and ability for chondrogenic and osteogenic differentiation, seeded on scaffolds, and cultured for up to 4 weeks. Histological analysis and microcomputer tomography showed the development of up to 1.2‐mm‐long interconnected and organized bonelike trabeculae with cuboid cells on the silk‐RGD scaffolds, features still present but to a lesser extent on silk scaffolds and absent on the collagen scaffolds. The X‐ray diffraction pattern of the deposited bone corresponded to hydroxyapatite present in the native bone. Biochemical analysis showed increased mineralization on silk‐RGD scaffolds compared with either silk or collagen scaffolds after 4 weeks. Expression of bone sialoprotein, osteopontin, and bone morphogenetic protein 2 was significantly higher for hMSCs cultured in osteogenic than control medium both after 2 and 4 weeks in culture. The results suggest that RGD‐silk scaffolds are particularly suitable for autologous bone tissue engineering, presumably because of their stable macroporous structure, tailorable mechanical properties matching those of native bone, and slow degradation. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res 71A: 25–34, 2004

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