Recent improvements in microsurgical techniques on lymphatic vessels f
acilitated the treatment of lymphoedema. But it is becoming clear that
a successful treatment of lymphatic disease has to be based on knowle
dge of ongoing processes. Particularly, one of the important and uncle
ar issue is cellular mechanisms of lymphatic regeneration. The regener
ation of endothelial and the smooth muscle cells of the thoracic duct
has been experimentally tested in vivo. The canine and feline thoracic
duct was cryo-injured using 3 mm-based copper rod. Damaged endothelia
l cells remained attached to the substrate and lost unthrombogenecy wi
thin 48 hr. Adjacent EC restored the defect within 3 days by migration
and proliferation. We observed that on the first day, the endothelial
monolayer included some elongated multinuclear cells with blind silve
r lines whereas, on the third day, they were replaced by a population
of smaller ECs with numerous mitoses. Organization of the monolayer wa
s restituted within 7 days. The newly formed endothelium was similar t
o regenerating endothelium of arteries. In general, the clot that appe
ared at the zone of injury on the second day was dissolved by the thir
d day. Occasionally, the dense polymorphic clot adhered to the wall an
d caused a delay in reendothelisation. Complete restitution of the tun
ica media which involved migration and proliferation mechanisms accomp
anied the endothelium regeneration.