DYNAMIC ASSESSMENT OF INTRASPINAL NEURAL GRAFT-SURVIVAL USING MAGNETIC-RESONANCE-IMAGING

Citation
Ed. Wirth et al., DYNAMIC ASSESSMENT OF INTRASPINAL NEURAL GRAFT-SURVIVAL USING MAGNETIC-RESONANCE-IMAGING, Experimental neurology, 136(1), 1995, pp. 64-72
Citations number
31
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00144886
Volume
136
Issue
1
Year of publication
1995
Pages
64 - 72
Database
ISI
SICI code
0014-4886(1995)136:1<64:DAOING>2.0.ZU;2-1
Abstract
Although previous work has demonstrated the usefulness of magnetic res onance imaging (MRI) for visualizing intraspinal transplants in vivo t he degree to which MRI can differentiate viable fetal neural tissue fr om evolving spinal cord pathology has not been investigated. Thus, the present study assessed whether MRI performed at earlier postgrafting intervals (0-20 weeks) could document the survival of fetal neural tra nsplants in the injured cat spinal cord. Twelve adult female cats rece ived a hemisection injury at the L(1) level, followed immediately by i mplantation of either embryonic cat spinal cord or neocortex into the cavity. The spinal cords of three control animals were hemisected but received no transplant. Each animal was subsequently imaged at 4 and 8 weeks postoperative. Selected animals from each group were also studi ed at additional time points ranging hom immediately postoperative to 20 weeks. Multislice T-2-weighted and intermediate T-1-weighted spin-e cho images of the lesion or graft site were obtained. Correlative post mortem histological analyses revealed viable donor tissue in 6 of 12 t ransplant recipients. Spinal cords from the remaining hosts and the co ntrol animals all contained cysts at the surgical site that were devoi d of donor neural tissue. The graft sites with viable tissue tended to exhibit a slightly hyperintense signal on both intermediate T-1-weigh ted (T1WI) and T-2-weighted images (T2WI) throughout the entire experi ment. Control cats and cats with failed transplants also were slightly bright on T1WI, but were very hyperintense on T2WI. Comparison of the normalized mean pixel intensity on T1WI at the lesion or transplant e picenter showed no significant differences between viable grafts, fail ed grafts, and controls at any time point studied. In contrast, viable grafts had significantly less signal than both failed grafts and cont rol lesions on T2WI at 4, 8, and 12 weeks postoperative. We conclude t hat transplant survival may be observed as early as 2 to 4 weeks postg rafting by the presence of medium signal intensity on T-2-weighted ima ges. In addition, T1WI were not useful for predicting graft survival, but aided in defining the graft or lesion boundaries. (C) 1995 Academi c Press, Inc.