Br. Southwell et al., MOVEMENT OF VILLI INDUCES ENDOCYTOSIS OF NK1 RECEPTORS IN MYENTERIC NEURONS FROM GUINEA-PIG ILEUM, Cell and tissue research, 292(1), 1998, pp. 37-45
Agitation of villi evokes reflexes that affect the motility of the gui
nea-pig small intestine. NK1 receptor endocytosis was used to investig
ate the possible involvement of tachykinins acting on neuronal NK1 rec
eptors in these reflexes, Segments of guinea-pig ileum were incubated
at 37 degrees C in Krebs physiological saline containing 3x10(-6) M ni
cardipine, with or without agitation of the villi by gas bubbles. Gut
segments were fixed after 0-75 min and processed for immunohistochemis
try to reveal the NK1 receptors, following which cells were imaged by
confocal microscopy. Initially, receptors were located on the surface
and in the cytoplasm of myenteric neurons. In gut incubated without mo
vement of the villi, NK1 receptors returned to the cell surface. After
45 and 60 min, NK1 receptors were detected almost exclusively at the
cell surface of 83% and 97% (respectively) of nerve cells that were im
munoreactive for NK1 receptors and only 12%-13% of the NK1 receptor fl
uorescence was located in the cytoplasm. Following the return of recep
tor to the cell surface, agitation of the villi caused a new wave of e
ndocytosis of the NK1 receptors in 70%-80% of the NK1 receptor-immunor
eactive neurons. The percentage of the NK1 receptor fluorescence that
was in the cytoplasm increased more than 2-fold to 27+/-2% after 15 mi
n villous agitation. Action potential blockade by tetrodotoxin (3x10(-
7) M) prevented the internalisation of the NK1 receptor in response to
villous agitation. The degree of internalisation caused by bubbling w
as similar to that caused by 2x10(-9) M substance P. These results ind
icate that, when enteric reflex circuits are activated by villous move
ment, tachykinins are released and cause endocytosis of the NK1 recept
or in a subpopulation of myenteric neurons.