a1–a5) Whole cell reconstructions of biplexiform melanopsin ganglion
cells with each type of ORD morphology at P12. Images are depth-coded so that
black represents dendrites or somas in the GCL and IPL, blue represents
dendrites or somas in the INL, and green represents dendrites that stratify in
the OPL. Both M1 and M1d cells are known to have dendrites that stratify in the
S1 plexus, so arrows indicate dendrites that can be seen in both the whole cell
tracings and the confocal images of the S1 plexus to the right. From top to
bottom: M1 with an unbranched ORD, M1 with a branched ORD, M1d with an
unbranched ORD, M1d with a branched ORD, and M1d with an ORD in the OPL as well
as an ORD in the INL. b1–b5) Confocal optical sections (0.50 μm)
of the melanopsin-immunopositive S1 plexus (magenta). Arrows indicate dendrites
in the S1 plexus that can also be seen in the respective whole cell tracings in
the first column. c1–c5) Confocal optical sections (0.50 μm) of
the melanopsin-immunopositive S1 plexus (magenta). Dendrites that are present in
both the whole cell tracing and the S1 plexus have been highlighted for clarity.
Arrows indicate dendrites in the S1 plexus that can also be seen in their
respective whole cell tracings in the first column. d1–d5) A single
optical section (0.50 μm) generated from a series of confocal images
masked to correct for the imperfect flatness of the retina. Immunopositive
melanopsin ORDs stratifying in the OPL (magenta). e1–e5) 3D projections
of confocal z-stacks (magenta=melanopsin, green=VGLUT1) to show
the 21 biplexiform nature of a subset of M1 and M1d melanopsin ganglion cells.
a1–d5 scale bars: 50 μm; e1–e5 scale bar: 25
μm.