Yd. Stierhof et al., CHARACTERIZATION OF POLYMER RELEASE FROM THE FLAGELLAR POCKET OF LEISHMANIA-MEXICANA PROMASTIGOTES, The Journal of cell biology, 125(2), 1994, pp. 321-331
Trypanosomatids contain a unique compartment, the flagellar pocket, fo
rmed by an invagination of the plasma membrane at the base of the flag
ellum, which is considered to be the sole cellular site for endocytosi
s and exocytosis of macromolecules. The culture supernatant of Leishma
nia mexicana promastigotes, the insect stage of this protozoan parasit
e, contains two types of polymers: a filamentous acid phosphatase (sAP
) composed of a 100-kD phosphoglycoprotein with non-covalently associa
ted proteo high molecular weight phosphoglycan (proteo-HMWPG) and fibr
ous material termed network consisting of complex phosphoglycans. Secr
etion of both polymers is investigated using mAbs and a combination of
light and electron microscopic techniques. Long filaments of sAP are
detectable in the lumen of the flagellar pocket. Both sAP filaments an
d network material emerge from the ostium of the flagellar pocket. Whi
le sAP filaments detach from the cells, the fibrous network frequently
remains associated with the anterior end of the parasites and can be
found in the center of cell aggregates. The related species L. major f
orms similar networks. Since polymeric structures cannot be detected i
n intracellular compartments, it is proposed that monomeric or, possib
ly, oligomeric subunits synthesized in the cells are secreted into the
flagellar pocket. Polymer formation from subunits is suggested to occ
ur in the lumen of the pocket before release into the culture medium o
r, naturally, into the gut of infected sandflies.