Implantation of a New Porous Gelatin–Siloxane Hybrid into a Brain Lesion as a Potential Scaffold for Tissue Regeneration

Author:

Deguchi Kentaro12,Tsuru Kanji3,Hayashi Takeshi1,Takaishi Mikiro2,Nagahara Mitsuyuki3,Nagotani Shoko1,Sehara Yoshihide1,Jin Guang1,Zhang HanZhe1,Hayakawa Satoshi3,Shoji Mikio1,Miyazaki Masahiro2,Osaka Akiyoshi3,Huh Nam-Ho2,Abe Koji1

Affiliation:

1. Department of Neurology, Graduate School of Medicine, Dentistry and Pharmacy, Faculty of Engineering, Okayama University, Okayama, Japan

2. Department of Cell Biology, Graduate School of Medicine, Dentistry and Pharmacy, Faculty of Engineering, Okayama University, Okayama, Japan

3. Biomaterial Laboratory, Faculty of Engineering, Okayama University, Okayama, Japan

Abstract

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 gelatin–siloxane 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.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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