K. Torigoe et G. Lundborg, SELECTIVE-INHIBITION OF EARLY AXONAL REGENERATION BY MYELIN-ASSOCIATED GLYCOPROTEIN, Experimental neurology, 150(2), 1998, pp. 254-262
When the distal stump of a transected peripheral nerve is brought: int
o the vicinity of the proximal nerve stump, the regenerating axons adv
ance toward it across the gap, Similar results are obtained when a pre
degenerated nerve segment is used, However, when a nerve segment subje
cted to proximal axotomy 7 days earlier (7-day nerve segment) was plac
ed close to the proximal and of a freshly cut nerve at a distance of l
ess than 1.5 mm, there were neither regenerating axons nor sprouts. Th
e same inhibition of axonal regeneration was also exhibited when a ner
ve segment subjected to axotomy 9 to 14 days earlier was used, To exam
ine the inhibitory effect of the nerve segments on established regener
ating axons, we positioned a 7-day nerve segment in close apposition t
o a proximal nerve end at 2 or 3 days after transection. The growth of
the 3-day-old regenerating axons, already ensheathed by Schwann cells
, was not disturbed, but the 2-day-old regenerating axons, consisting
of naked axons, were eliminated by the 7-day nerve segment, It is assu
med that the findings reflect a mechanism serving to eliminate abundan
t sprouts and immature axons, probably conferencing optimum regenerati
on and maturation of outgrowing pioneer axons, The inhibitory effect o
n abundant sprouts and immature axons was completely blocked by local
application of antibodies to myelin-associated glycoprotein (MAG), The
MAG-containing cells appeared at 6 to 12 days after axotomy. (C) Acad
emic Press.