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. Author manuscript; available in PMC: 2013 Jul 14.
Published in final edited form as: Dev Biol. 2012 May 1;365(1):152–163. doi: 10.1016/j.ydbio.2012.02.022

Figure 7. Timing of cell cycle exit in the geniculate ganglion.

Figure 7

Cumulative BrdU labeling was performed in two litters of embryos, beginning early and late on gestational day E10.5 (designated “E10.4” and “E10.6”, see text). (A–C) In the later-labeled embryos, nearly all Hmx1-expressing neurons in the geniculate ganglion (circled) have exited the cell cycle by the start of the labeling period in both control and Hmx1dm/dm embryos. (D,E) In the dorsal geniculate ganglion (circled) of earlier-labeled embryos, some geniculate neurons are still undergoing (a presumably final round) of DNA synthesis at the onset of labeling. A similar fraction of BrdU-positive neurons are observed in the geniculate ganglion of control and Hmx1dm/dm embryos. (F–H) In the ventral geniculate ganglion (circled) of earlier-labeled embryos, only a few Hmx1-expressing somatosensory neurons are present; most of the ganglion at this level consists of Hmx1-negative viscerosensory neurons. Hmx1 neurons at this level have mostly exited the cell cycle by the stage of labeling. Hmx1 expression also identifies a population of early-born neurons in the statoacoustic ganglion. Neither population shows altered incorporation of BrdU in Hmx1dm/dm embryos. GG, geniculate ganglion; OV, otic vesicle; SAG, statoacoustic ganglion. Scale, 100μm.