Small intestine submucosa as a growth factor attractor promotes peripheral nerve regeneration by enhancing syndecan-3/glial cell line-derived neurotrophic factor (GDNF) signalling: in vivo study *

被引:2
作者
Liu, Chiung-Hui [1 ,2 ]
Chu, Yin-Hung [1 ]
Chen, Yin Hsiu [3 ]
Chiang, Yu Hsin [3 ]
Chen, Yu Hsuan [3 ]
Ku, Chung Yao [3 ]
Hsu, Min-Yen [3 ,4 ]
Lee, Yi-Ju [5 ,6 ]
Yang, Mao-Yi [7 ]
Liao, Wen-Chieh [1 ,2 ]
机构
[1] Natl Chung Hsing Univ, Coll Med, Doctoral Program Tissue Engn & Regenerat Med, 145 Xingda Rd, Taichung 40227, Taiwan
[2] Natl Chung Hsing Univ, Coll Med, Dept Postbaccalaureate Med, 145 Xingda Rd, Taichung 40227, Taiwan
[3] Chung Shan Med Univ, Sch Med, 110,Sec1,Jianguo N Rd, Taichung 40201, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Ophthalmol, Taichung 40201, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Pathol, Taichung 40201, Taiwan
[6] Chung Shan Med Univ, Dept Pathol, Taichung 40201, Taiwan
[7] Shin Kong Wu Ho Su Mem Hosp, Dept Orthoped Surg, 95 Wen Chang Rd, Taipei 11101, Taiwan
关键词
small intestine submucosa; syndecan-3 (SDC3); glial cell-derived growth factor (GDNF); nerve regeneration; end-to-side neurorrhaphy; peripheral nerve injury; HEPARAN-SULFATE PROTEOGLYCANS; EXTRACELLULAR-MATRIX; AXON REGENERATION; SCHWANN-CELLS; INJURY; IMPLANTATION; BIOSCAFFOLD; EXPRESSION; OUTCOMES; CONDUIT;
D O I
10.1088/1748-605X/acdeb9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Peripheral nerve regeneration (PNR) following trauma requires the reconstruction of the extracellular matrix (ECM) and the proper stimulation of growth factors. Decellularised small intestine submucosa (SIS) has been extensively used as an ECM scaffold for tissue repair, but its potential to enhance the effects of exogenous growth factors on PNR is not well understood. In this study, we evaluated the effects of SIS implantation combined with glial cell-derived growth factor (GDNF) treatment on PNR in a rat neurorrhaphy model. We found that both SIS and regenerating nerve tissue expressed syndecan-3 (SDC3), one of major heparan sulphate proteoglycans in nerve tissue, and that SDC3 interacted with GDNF in the regenerating nerve tissue. Importantly, the SIS-GDNF combined treatment enhanced the recovery of neuromuscular function and & beta;3-tubulin-positive axonal outgrowth, indicating an increase in the number of functioning motor axons connecting to the muscle after neurorrhaphy. Our findings suggest that the SIS membrane offers a new microenvironment for neural tissue and promotes neural regeneration based on SDC3-GDNF signalling, providing a potential therapeutic approach for PNR.
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页数:14
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