L. Schnell et Me. Schwab, SPROUTING AND REGENERATION OF LESIONED CORTICOSPINAL TRACT FIBERS IN THE ADULT-RAT SPINAL-CORD, European journal of neuroscience, 5(9), 1993, pp. 1156-1171
We have studied the effects of tissue transplants and antibodies (IN-1
) against the myelin-associated neurite growth inhibitory proteins on
sprouting and regeneration of the rat corticospinal tract (CST). Trans
plantation of embryonic spinal cord tissue into bilateral transection
lesions of the lower thoracic spinal cord in young adult rats resulted
in a marked increase of the sprouting of the lesioned CST. This sprou
ting effect was probably elicited by soluble factors released from the
transplants, and was enhanced by the IN-1 antibodies. The retraction
of lesioned CST fibres normally observed with prolonged survival times
was also reduced by the presence of transplants. In spite of these gr
owth-promoting effects of the transplants, the regenerative elongation
of CST sprouts into the caudal spinal cord was dependent upon the neu
tralization of the myelin-associated inhibitory proteins. In the contr
ols (no antibodies or control antibodies) only 27% of the animals show
ed elongation of CST fibres exceeding the sprouting distance of 0.7 mm
. These fibres grew to a maximal length of 1.8 mm (mean +/- SEM, 1.2 /- 0.1). In contrast, 60% of the IN-1-treated, transplant-containing r
ats showed elongations of >0.7 mm, and these fibres grew up to 10.1 mm
(4.6 +/- 0.5). Regenerating fibres crossed the lesion site through re
maining tissue bridges. Neither embryonic spinal cord transplants nor
a variety of implanted bridge materials could serve as a substrate for
the regenerating CST axons.