Fig. 7
Insulin signaling blockade in transplanted endodermal committed blastomeres promotes Pdx1 expression. (A) Scheme of endoderm replacement transplantation experiments. sox32-injected blastomeres termed “Endoderm Committed Blastomeres” (ECBs) were isolated from donor Tg(sox17:GFP) blastulae with or without injected dnIRS2-GFP mRNA. ECBs were transplanted into endoderm deficient, sox32MO-injected host blastulae. (B) 24 hpf chimera shows extensive replacement of endogenous endoderm with transplanted Tg(sox17:GFP) donor cells. (C–D′′) Merged and single channel confocal projections of 24 hpf embryos with endoderm transplants from sox32 mRNA (C–C3, n=8) or sox32 and dnIRS2 mRNA (D–D′′, n=7) injected donors. Embryos were immunostained for GFP (green), Pdx1 (red), and DNA (blue). dnIRS2-GFP-expressing endoderm showed increased Pdx1 expression.
Reprinted from Developmental Biology, 409(2), Ye, L., Robertson, M.A., Mastracci, T.L., Anderson, R.M., An insulin signaling feedback loop regulates pancreas progenitor cell differentiation during islet development and regeneration, 354-69, Copyright (2016) with permission from Elsevier. Full text @ Dev. Biol.