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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: Dev Dyn. 2013 Mar 6;242(5):550–559. doi: 10.1002/dvdy.23928

Figure 4. tbx1 is required for SHF progenitor cell maintenance.

Figure 4

(A–B) ltbp3 was observed via whole-mount in situ hybridization at 20.5hpf/23ss in control (A) and vgo (B) embryos (n>12). Dorsal view, anterior down. 20X Magnification. (C, D) Whole-mount double in situ hybridization at 26 hpf shows ltbp3+ (blue) cells at the arterial pole (arrowhead) of the cmlc2+ (red) heart tube in control embryos. ltbp3 expression is drastically reduced (21%) or absent (79%) at the arterial pole of vgo hearts (n=14). Asterisk indicates ltbp3 expression within the notochord. (E, F) Double transgenic Tg(nkx2.5::ZsYellow); Tg(cmlc2::GFP) control (E) and vgo (F) embryos co-immunostained with GFP antibody (anti-GFP, green) and ZsYellow antibody (anti-RCFP, red) at 26 hpf. The future atrial segment of the linear heart tube (LHT, green arrow) expresses cmlc2 alone (green), while the future proximal ventricular myocardium co-expresses cmlc2 and nkx2.5 (yellow). Non-myocardial nkx2.5+ second heart field (SHF) progenitors (red arrow) can be visualized in control animals (n=8), but are lacking in vgo mutants (n=7).