Ht. Liu et al., COINJECTION OF WHEAT-GERM AGGLUTININ-HRP AND CHOLERAGENOID-HRP INTO THE SCIATIC-NERVE OF THE RAT BLOCKS TRANSGANGLIONIC TRANSPORT, The Journal of histochemistry and cytochemistry, 43(5), 1995, pp. 489-495
We report on the surprising loss of transganglionic and retrograde lab
eling in the spinal cord of the rat after co-injection of the tracers
wheat germ agglutinin-HRP (WGA-HRP) and choleragenoid toxin-HRP (CTB-H
RP) into the sciatic nerve. Injection of WGA-HRP alone produced a patt
ern of transganglionic label consistent with transport by small-diamet
er primary afferent fibers. Small cell bodies were labeled in the ipsi
lateral dorsal toot ganglion (DRG) and there was dense terminal labeli
ng in the superficial dorsal horn of the lumbar spinal cord. Injection
of CTB-HRP alone produced a pattern of transganglionic labeling consi
stent with transport by large-diameter primary afferent fibers. Large
cell bodies were labeled in the DRG and there was dense terminal label
ing in the nucleus proprius (Laminae III-V) in the spinal cord. CTB-HR
P also produced extensive retrograde labeling of ventral horn motor ne
urons. When the two tracers were co-injected, we found few labeled cel
ls in the ipsilateral DRG and there was almost complete loss of transg
anglionic terminal labeling in the lumbar spinal cord. Retrograde labe
ling of motor neurons was also significantly reduced. Even when one of
the tracers (e.g., WGA-HRP) was injected 24 hr after and up to 10 mm
proximal to the site of the first tracer (e.g., CTB-HRP), an inhibitor
y interaction was detected. The labeling pattern was always characteri
stic of the first tracer injected. Since the loss of labeling was obse
rved in the DRG and in the spinal cord, we conclude that the mutually
inhibitory interactions occur during uptake of the tracers by the scia
tic nerve and/or in the mechanism of transport to the dorsal root gang
lion and beyond. The fact that reduced labeling was observed even when
the injections were separated temporally and spatially suggests that
the underlying mechanism is more complicated than mere creation of a W
GA-HRP/CTB-HRP complex that cannot be taken up and transported by the
sciatic nerve.