Immunofluorescence staining of Gli in the osmoregulatory tissues of Aedes aegypti larva. Immunofluorescence staining of Gli in the osmoregulatory tissues.

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Immunofluorescence staining of Gli in the osmoregulatory tissues of Aedes aegypti larva. Immunofluorescence staining of Gli in the osmoregulatory tissues of Aedes aegypti larva. Gli was localized to regions of cell–cell contact between the epithelial cells of the gastric caecae (A), and anterior and posterior midgut (B–D). In the Malpighian tubules, Gli immunostaining appears to be confined to the contact regions between the stellate and principal cells (SC and PC, respectively; arrows in F and G) in the distal two-thirds of the tubule (E–H) as compared with the expression of the stellate cell marker AeAE (I–K, green). (L) Brightfield image of K. Gli also shows some discontinuous immunostaining along the plasma membranes of the epithelial cells in the rectum (M; shown also are outlined rectal cell boarders) and anal papillae epithelium (N), where it exhibits some co-immunoreactivity with apical V-type H+-ATPase (VA; O, green). Nuclei of anal papilla epithelium are stained with DAPI (blue) in N. (P) Control sections of anal papillae treated with anti-Gli antibody in the presence of immunizing peptide (Pt) and only DAPI (blue) staining is observed. Scale bars: (A,C,D,F) 20 µm, (B,E,G–K,L,M–P) 50 µm. GC, gastric caecae; AMG, anterior midgut; PMG, posterior midgut; MT, Malpighian tubules; AP, anal papillae. Sima Jonusaite et al. J Exp Biol 2017;220:2354-2363 © 2017. Published by The Company of Biologists Ltd