Antheraea pernyi silk sericin mediating biomimetic nucleation and growth of hydroxylapatite crystals promoting bone matrix formation. Issue 3 (18th November 2016)

• Record Type: Journal Article
• Authors: Jiayao, Zhuang; Guanshan, Zhou; Jinchi, Zhang; Yuyin, Chen; Yongqiang, Zhu
• Other Names: Yang Mingying guestEditor.
• Is Part Of: Microscopy research and technique. Volume 80:Issue 3(2017)
• Page Start: 305
• Page End: 311
• Publication Date: 2016-11-18
• Subjects: biomineralization -- Antheraea pernyi (A.pernyi) sericin -- hydroxylapatite crystals -- human bone marrow‐derived mesenchymal stem cells; Electron microscopy -- Technique -- Periodicals; Microscopy -- Periodicals; Microscopy -- Technique -- Periodicals; 502.825
• DOI: 10.1002/jemt.22793
• Languages: English
• ISSNs: 1059-910X

Abstract

Abstract: Bone biomineralization is well‐regulated processes mediated by extracellular matrix proteins. The materials that can direct nucleation of hydroxylapatite (HAp) crystals and assembly of well‐structured material‐minerals complex are the key to mimicking the natural mineralization. This study used sericin from Antheraea pernyi ( A.pernyi ), non‐mulberry silkworm cocoon as template to mediate nucleation of HAp crystals. Here we find out that AS (Antheraea pernyi sericin) can nucleate the formation HAp crystals in simulated body fluid verified by XRD and FTIR observations. The HAp crystals are organized into nano‐rods oriented with c‐axis preferentially parallel to the long axis of AS due to hydrogen bonds and electrostatic interaction and finally aggregated into HAp globule. The cell culture of human bone marrow‐derived mesenchymal stem cells (BMSCs) showed that the HAp crystals mediated by AS not only stimulate cell adhesion and proliferation but also promote 0f osteogenic differentiation, suggesting that the resultant mineralized AS biomaterial has potential in promoting bone formation. Thus our work will provide significant implication on biomineralization of A. pernyi silk sericin as a potential scaffold for tissue engineering.