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Growth factor-free, angiogenic hydrogel based on hydrophobically modified Alaska pollock gelatin
被引:9
|作者:
Mizuno, Yosuke
[1
]
Taguchi, Tetsushi
[1
,2
]
机构:
[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki, Japan
[2] Natl Inst Mat Sci, Res Ctr Funct Mat, Biomat Field, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
基金:
日本学术振兴会;
关键词:
Alaska pollock-derived gelatin;
angiogenesis;
inflammation;
saturated fatty acid;
TLR4;
VEGF;
REDUCTIVE AMINATION;
MODULATION;
EXPRESSION;
ALDEHYDES;
KETONES;
ALPHA;
D O I:
10.1002/term.2957
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Angiogenesis is important for supplying oxygen and nutrients to implanted cells and organs and thereby promoting their survival. However, exogenously administered growth factors such as vascular endothelial growth factor (VEGF) have a short half-life and are unstable under physiological conditions. In the present study, we developed an angiogenesis-inducing hydrogel by modifying Alaska pollock-derived gelatin with a dodecyl group (C12-ApGltn), and demonstrated that it is biodegradable and highly fluid at room temperature (25 degrees C). C12-ApGltn dissolved in phosphate-buffered saline at 20 w/v% formed a self-assembling hydrogel with thixotropic properties that stimulated VEGF secretion by macrophage-like RAW264 cells. Moreover, C12-ApGltn stimulated nuclear factor-kappa B and VEGF expression when subcutaneously injected into mice and increased the cluster of differentiation 31-positive area compared with injection of unmodified ApGltn and phosphate-buffered saline control in the absence of any growth factors. Hematoxylin and eosin staining confirmed vascular capillaries around the C12-ApGltn injection site. These results demonstrate that C12-ApGltn hydrogel is a promising angiogenic material for clinical applications that can stimulate endogenous VEGF expression without requiring additional growth factors.
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页码:2291 / 2299
页数:9
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