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. Author manuscript; available in PMC: 2015 Jul 17.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2005 Jun;46(6):2156–2167. doi: 10.1167/iovs.04-1427

Table 1.

Features of Nrl–/– Photoreceptors Compared with Those of WT Mouse Rods and Cones

Feature Nrl–/– Photoreceptors WT Cones WT Rods Figure (Current Study)
Ultrastructure
    OS length (μm) 7.3 ± 1.3 (21) 13.4 ± 0.7* 23.6 ± 0.4* Fig. 2
    OS width (μm) 1.2 ± 0.3 (21) 1.2 ± 0.03* 1.4 ± 0.1* Fig. 2
    OS volume (μm3) 8.3 14 36
    Open discs up to 30 >15* 5-7* Fig. 2
    Mitochondrial length (μm) 0.94 ± 0.38 (50) 1.31 ± 0.7 (13)* 2.20 ± 0.7 (15) Fig. 2
Histological
    Chromatin clumping Yes Yes No Fig. 1
    PNA-stained OS sheath Yes Yes No Fig. 3
Molecular
    MUV Yes Yes No Figs. 3-5
    Gtα2 Yes Yes No Fig. 5
    mCarr Yes Yes No Fig. 5
    Arrestin Yes Yes, low level Yes
ERG a-wave
    λmax (nm) 360 360 500 Fig. 6
    tpeak (ms) ≈50 unknown 140§ Fig. 7

The first column gives a list of the features on which Nrl–/– photoreceptors, WT rods, and WT cones are compared. Entries summarize data from this investigation or from previously published work. Error terms are standard deviations; numbers following in parentheses give sample size.

*

Carter-Dawson and LaVail.28

Mears et al.5

Craft and Zhu, personal communication, 2004.

§

Hetling and Pepperberg,41 who used the paired-flash method to extract rod responses from WT mice, as was used in the present study in Nrl–/– mice.