Implantation of a new porous gelatin-siloxane hybrid into a brain lesion as a potential scaffold for tissue regeneration

被引:51
作者
Deguchi, Kentaro
Tsuru, Kanji
Hayashi, Takeshi
Takaishi, Mikiro
Nagahara, Mitsuyuki
Nagotani, Shoko
Sehara, Yoshihide
Jin, Guang
Zhang, HanZhe
Hayakawa, Satoshi
Shoji, Mikio
Miyazaki, Masahiro
Osaka, Akiyoshi
Huh, Nam-Ho
Abe, Koji
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharm, Dept Neurol, Fac Engn, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharm, Dept Cell Biol, Fac Engn, Okayama 7008558, Japan
[3] Okayama Univ, Fac Engn, Biomat Lab, Okayama 7008558, Japan
关键词
brain tissue defect; porous gelatin-siloxane hybrid; scaffold; tissue regeneration;
D O I
10.1038/sj.jcbfm.9600275
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For brain tissue regeneration, any scaffold for migrated or transplanted stem cells with supportive angiogenesis is important once necrotic brain tissue has formed a cavity after injury such as cerebral ischemia. In this study, a new porous gelatin-siloxane hybrid derived from the integration of gelatin and 3-(glycidoxypropyl) trimethoxysilane was implanted as a three-dimensional scaffold into a defect of the cerebral cortex. The porous hybrid implanted into the lesion remained at the same site for 60 days, kept integrity of the brain shape, and attached well to the surrounding brain tissues. Marginal cavities of the scaffolds were occupied by newly formed tissue in the brain, where newly produced vascular endothelial, astroglial, and microglial cells were found with bromodeoxyuridine double positivity, and the numbers of those cells were dose-dependently increased with the addition of basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF). Extension of dendrites was also found from the surrounding cerebral cortex to the newly formed tissue, especially with the addition of bFGF and EGF. The present study showed that a new porous gelatinsiloxane hybrid had biocompatibility after implantation into a lesion of the central nervous system, and thus provided a potential scaffold for cell migration, angiogenesis and dendrite elongation with dose-dependent effects of additive bFGF and EGF.
引用
收藏
页码:1263 / 1273
页数:11
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