S. Torihashi et al., IDENTIFICATION AND CLASSIFICATION OF INTERSTITIAL-CELLS IN THE CANINEPROXIMAL COLON BY ULTRASTRUCTURE AND IMMUNOCYTOCHEMISTRY, Histochemistry, 101(3), 1994, pp. 169-183
The ultrastructure and immunocytochemistry of interstitial cells (ICs)
in the canine proximal colon were investigated. Three types of ICs we
re found within the tunica muscularis. (1) ICs were located along the
submucosal surface of the circular muscle (IC-SM). These cells shared
many features of smooth muscle cells, including myosin thick filaments
and immunoreactivity to smooth muscle gamma actin, myosin light chain
, and calponin antibodies. IC-SM were clearly different from smooth mu
scle cells in that contractile filaments were less abundant and interm
ediate filaments consisted of vimentin instead of desmin. (2) ICs in t
he region of the myenteric plexus (IC-MY) were similar to IC-SM, but t
hese cells had no thick filaments or immunoreactivity to smooth muscle
gamma actin or calponin antibodies. (3) The fine structures and immun
oreactivity of ICs within the muscle layers (IC-BU) were similar to IC
-MY, but IC-BU lacked a definite basal lamina and membrane caveolae. I
C-BU and IC-MY were both immunopositive for vimentin. Since all ICs we
re immunopositive for vimentin, vimentin antibodies may be a useful to
ol for distinguishing between ICs and smooth muscle cells. Each class
of ICs was closely associated with nerve fibers, made specialized cont
acts with smooth muscle cells, and formed multicellular networks. A co
mbination of ultrastructural and immunocytochemical techniques helps t
he identification and classification of ICs by revealing the fine stru
ctures and determining the ''chemical coding'' of each class of ICs.