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Resolution: standard / high Figure 4.
Some distinct features of UAS-ara overexpressing cells. UAS-ara expressing cells (green) were detected by coexpression of UAS-GFP, except in F and G where they were labelled with an anti Ara/Caup antibody. Counterstaining
(in red) was Actin (B-D, F, G) or E-Cadherin (E). (A, A') UAS-ara-expressing cells distort the prospective wing margin (anti Cut staining, purple)
by apparently pulling on it (arrowheads). (B, B') Apical x, y section of a connecting stripe between larger masses of UAS-ara expressing cells.
Cell contours (arrowheads) are stretched parallel to the longitudinal axis of the
stripe. (C, D) xy and z optical sections, respectively, of a small group of wild-type cells surrounded by
UAS-ara-expressing cells. The former undergo apical-basal shortening (arrowheads). (E) z section of a group of wild-type cells surrounded by UAS-ara expressing cells. The apical marker DE-Cadherin shows that a fold has been formed
at the interface (arrowheads). (F, G) xy and z optical sections, respectively, of UAS-ara expressing clones that have induced folds of the wing pouch epithelium (arrowheads)
that comprise overexpressing and non-expressing cells. The folds can join with the
extant folds of the disc (arrow). Dashes mark the approximate plane of the reciprocal
view. For orientation, blue arrows in D, E and G point towards the apical part of
cells.
Villa-Cuesta et al. BMC Developmental Biology 2007 7:106 doi:10.1186/1471-213X-7-106 |