Ed. Wirth et al., DYNAMIC ASSESSMENT OF INTRASPINAL NEURAL GRAFT-SURVIVAL USING MAGNETIC-RESONANCE-IMAGING, Experimental neurology, 136(1), 1995, pp. 64-72
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.