BioPEGylation of Polyhydroxybutyrate Promotes Nerve Cell Health and Migration

被引:32
作者
Chan, Rodman T. H. [1 ]
Russell, Robert A. [1 ,3 ]
Marcal, Helder [1 ]
Lee, Terry H. [2 ]
Holden, Peter J. [3 ]
Foster, L. John R. [1 ]
机构
[1] Univ New S Wales, Biopolymer Res Grp, Ctr Adv Macromol Design, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
[2] Univ New S Wales, Infect & Inflammat Res Ctr, Sch Med Sci, Sydney, NSW, Australia
[3] Australian Nucl Sci & Technol Org, Lucas Heights, NSW, Australia
关键词
OLFACTORY ENSHEATHING CELLS; AXONS IN-VITRO; POLY(ETHYLENE GLYCOL); SCHWANN-CELLS; MOLECULAR-WEIGHT; NOGO-A; POLY(BETA-HYDROXYBUTYRATE); POLY(3-HYDROXYBUTYRATE); POLYHYDROXYALKANOATES; BIOCOMPATIBILITY;
D O I
10.1021/bm401572a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study reports on the superior suitability of Polyhydroxybutyrate-polyethylene glycol hybrid polymers biosynthesised by Cupriavidus necator over PHB as biomaterials for tissue engineering. Incorporation of PEG 106 (DEG) during PHB biosynthesis reduced crystallinity, molecular weight, and hydrophobicity while improving mechanical properties. In vitro olfactory ensheathing cell (OEC) proliferation was enhanced by cultivation on PHB-b-DEG films. Cultivation on PHB and PHB-b-DEG films showed no cytotoxic responses and cell viability and membrane integrity was sustained. PHB-b-DEG films promoted OECs entering into the DNA replication (5) phase and mitotic (G2-M) phase during the cell growth cycle and apoptosis was low. This study also confirmed an association between the level of neurite-outgrowth inhibitory protein (Nogo) and receptor pair Ig-like receptor B (PirB) expression and cell proliferation, both being down-regulated in cells grown on hybrid films when compared with PHB and asynchronous growth. Thus, DEG-terminated PHB-based biomaterials have great potential as biological scaffolds supporting nerve repair.
引用
收藏
页码:339 / 349
页数:11
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