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. 2024 Oct 11;13:e85042. doi: 10.7554/eLife.85042

Figure 6. Hh signal in mesoderm-derived cells.

(A, B) Double immunohistochemistry of YFP and Ptch1 on cultured YFP-expressing cranial neural crest-derived cells (CNCC) accompanied by YFP-negative mesoderm-derived cells (A) and only YFP-negative mesoderm-derived cells (B) obtained from Wnt1Cre;R26RYFP mice. (C) Double immunohistochemistry of YFP and Ptch1 in Wnt1Cre;R26RYFP mice. (D–G) Frontal images of whole-mount in situ hybridization of Myf5 (D) and Gli1 (E–G) in wild-type (D–F) and Ofd1fl;Wnt1Cre(HM) (G) at embryonic day (E) 10. (H) Double immunohistochemistry of YFP and MyoD on cultured YFP-negative mesoderm-derived cells obtained from Wnt1Cre;R26RYFP mice with (lower panels) or without (upper panels) SAG. Scale bars: 500 µm (D-G).

Figure 6.

Figure 6—figure supplement 1. Cyclopamine treated cranial neural crest-derived cells (CNCC) and mesoderm-derived cells.

Figure 6—figure supplement 1.

Double immunohistochemistry of YFP and Ptch1 on cultured YFP-expressing CNCC accompanied by YFP-negative mesoderm-derived cells obtained from Wnt1Cre;R26RYFP mice with cyclopamine.
Figure 6—figure supplement 2. Apoptosis and cell proliferation in Ofd1 mutant tongue.

Figure 6—figure supplement 2.

(A, B) Frontal sections showing Caspase-3 immunohistochemistry. (C) Comparison of the number of Caspase-3-positive cells between Wnt1Cre;R26RYFP mice and Ofd1fl;Wnt1Cre(HM);R26RYFP mice. (D, E) Frontal sections showing Ki67-positive cells. (F) Comparison of the number of Ki67-positive cells between Wnt1Cre;R26RYFP mice and Ofd1fl;Wnt1Cre(HM);R26RYFP mice.
Figure 6—figure supplement 2—source data 1. Percentage of Positive cells: Caspase-3 and Ki67.