PT  - JOURNAL ARTICLE
AU  - Eric M. Morrow
AU  - Michael J. Belliveau
AU  - Constance L. Cepko
TI  - Two Phases of Rod Photoreceptor Differentiation during Rat Retinal Development
AID  - 10.1523/JNEUROSCI.18-10-03738.1998
DP  - 1998 May 15
TA  - The Journal of Neuroscience
PG  - 3738--3748
VI  - 18
IP  - 10
4099  - http://www.jneurosci.org/content/18/10/3738.short
4100  - http://www.jneurosci.org/content/18/10/3738.full
SO  - J. Neurosci.1998 May 15; 18
AB  - We have conducted a comprehensive analysis of the relative timing of the terminal mitosis and the onset of rhodopsin expression in rod precursors in the rat retina in vivo. This analysis demonstrated that there are two distinct phases of rod development during retinal histogenesis. For the majority of rod precursors, those born on or after embryonic day 19 (E19), the onset of rhodopsin expression was strongly correlated temporally with cell cycle withdrawal. For these precursors, the lag between the terminal mitosis and rhodopsin expression was measured to be 5.5–6.5 d on average. By contrast, for rod precursors born before E19, the lag was measured to be significantly longer, averaging from 8.5 to 12.5 d. In addition, these early-born rod precursors seemed to initiate rhodopsin expression in a manner that was not correlated temporally with the terminal mitosis. In these cells, onset of rhodopsin expression appeared approximately synchronous with later-born cells, suggesting a synchronous recruitment to the rod cell fate induced by environmental signals. To examine this possibility, experiments in which the early-born precursors were exposed to a late environment were conducted, using a reaggregate culture system. In these experiments, the early-born precursors appeared remarkably uninfluenced by the late environment with respect to both rod determination and the kinetics of rhodopsin expression. These results support the idea that intrinsically distinct populations of rod precursors constitute the two phases of rod development and that the behavior exhibited by the early-born precursors is intrinsically programmed.