In vivo predegeneration of peripheral nerves: an effective technique to obtain activated Schwann cells for nerve conduits

被引:73
作者
Keilhoff, G
Fansa, H
Schneider, W
Wolf, G
机构
[1] Univ Magdeburg, Inst Med Neurobiol, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Dept Plast Reconstruct & Hand Surg, D-39120 Magdeburg, Germany
关键词
BrdU incorporation; fluorescence vital staining; in vivo predegeneration; Schwann cell culture; sciatic nerve;
D O I
10.1016/S0165-0270(99)00034-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In vivo predegeneration of peripheral nerves is presented as a convenient and effective method to obtain activated Schwann cells and an enhanced cell yield following in vitro cultivation. The experiments conducted in rats were aimed at clinical use in gaining Schwann cell suspensions for filling artificial conduits in order to bridge peripheral nerve gaps. The rat sciatic nerve used as a model was transected distally to the spinal ganglia. Predegeneration in vivo was allowed to take place for 1, 2, 3 and 4 days and up to 1, 2 and 3 weeks. The nerve was then resected and prepared for cell cultivation. Schwann cells cultivated from the contralateral untreated nerve served as control. Immunostaining for S100, nerve growth factor receptor and the adhesion molecules N-cadherin and L1 was used to characterize the general state of the cultures. Viability was assessed by fluorescein fluorescence staining, and the proliferation index was determined by bromodeoxyuridine-DNA incorporation. The Schwann cells from predegenerated nerves revealed an increased proliferation rate compared to the control, whereas fibroblast contamination was decreased. Best results were obtained 1 week after predegeneration. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:17 / 24
页数:8
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