Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse

Lauren L. Daniele, Conception Lillo, Arkady L. Lyubarsky, Sergei S. Nikonov, Nancy Philp, Alan J. Mears, Anand Swaroop, David S. Williams, Edward N Pugh Jr

Research output: Contribution to journalArticle

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Abstract

PURPOSE. To test the hypothesis that Nrl-/- photoreceptors are cones, by comparing them with WT rods and cones using morphological, molecular, histochemical, and electrophysiological criteria. METHODS. The photoreceptor layer of fixed retinal tissue of 4- to 6-week-old mice was examined in plastic sections by electron microscopy, and by confocal microscopy in frozen sections immunolabeled for the mouse UV-cone pigment and colabeled with PNA. Quantitative immunoblot analysis was used to determine the levels of expression of key cone-specific proteins. Single- and paired-flash methods were used to extract the spectral sensitivity, kinetics, and amplification of the a-wave of the ERG. RESULTS. Outer segments of Nrl-/- photoreceptors (∼7 μm) are shorter than those of wild-type (WT) rods (∼25 μm) and cones (∼15 μm); but, like WT cones, they have 25 or more basal discs open to the extracellular space, extracellular matrix sheaths stained by PNA, chromatin "clumping" in their nuclei, and mitochondria two times shorter than rods. Nrl-/- photoreceptors express the mouse UV cone pigment, cone transducin, and cone arrestin in amounts expected, given the relative size and density of cones in the two retinas. The ERG a-wave was used to assay the properties of the photocurrent response. The sensitivity of the Nrl -/- a-wave is at its maximum at 360 run, with a secondary mode at 510 nm having approximately one-tenth the maximum sensitivity. These wavelengths are the λmax of the two mouse cone pigments. The time to peak of the dim-flash photocurrent response was ∼50 ms, more than two times faster than that of rods. CONCLUSIONS. Many morphological, molecular, and electrophysiological features of the Nrl-/- photoreceptors are cone-like, and strongly distinguish these cells from rods. This retina provides a model for the investigation of cone function and cone-specific genetic disease.

Original languageEnglish (US)
Pages (from-to)2156-2167
Number of pages12
JournalInvestigative Ophthalmology and Visual Science
Volume46
Issue number6
DOIs
StatePublished - Jun 2005
Externally publishedYes

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Knockout Mice
Retinal Cone Photoreceptor Cells
Retina
Transducin
Arrestin
Vertebrate Photoreceptor Cells
Inborn Genetic Diseases
Specific Gravity
Extracellular Space
Frozen Sections
Confocal Microscopy
Plastics
Chromatin
Extracellular Matrix
Electron Microscopy
Mitochondria
Proteins

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse. / Daniele, Lauren L.; Lillo, Conception; Lyubarsky, Arkady L.; Nikonov, Sergei S.; Philp, Nancy; Mears, Alan J.; Swaroop, Anand; Williams, David S.; Pugh Jr, Edward N.

In: Investigative Ophthalmology and Visual Science, Vol. 46, No. 6, 06.2005, p. 2156-2167.

Research output: Contribution to journalArticle

Daniele, Lauren L. ; Lillo, Conception ; Lyubarsky, Arkady L. ; Nikonov, Sergei S. ; Philp, Nancy ; Mears, Alan J. ; Swaroop, Anand ; Williams, David S. ; Pugh Jr, Edward N. / Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse. In: Investigative Ophthalmology and Visual Science. 2005 ; Vol. 46, No. 6. pp. 2156-2167.
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T1 - Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse

AU - Daniele, Lauren L.

AU - Lillo, Conception

AU - Lyubarsky, Arkady L.

AU - Nikonov, Sergei S.

AU - Philp, Nancy

AU - Mears, Alan J.

AU - Swaroop, Anand

AU - Williams, David S.

AU - Pugh Jr, Edward N

PY - 2005/6

Y1 - 2005/6

N2 - PURPOSE. To test the hypothesis that Nrl-/- photoreceptors are cones, by comparing them with WT rods and cones using morphological, molecular, histochemical, and electrophysiological criteria. METHODS. The photoreceptor layer of fixed retinal tissue of 4- to 6-week-old mice was examined in plastic sections by electron microscopy, and by confocal microscopy in frozen sections immunolabeled for the mouse UV-cone pigment and colabeled with PNA. Quantitative immunoblot analysis was used to determine the levels of expression of key cone-specific proteins. Single- and paired-flash methods were used to extract the spectral sensitivity, kinetics, and amplification of the a-wave of the ERG. RESULTS. Outer segments of Nrl-/- photoreceptors (∼7 μm) are shorter than those of wild-type (WT) rods (∼25 μm) and cones (∼15 μm); but, like WT cones, they have 25 or more basal discs open to the extracellular space, extracellular matrix sheaths stained by PNA, chromatin "clumping" in their nuclei, and mitochondria two times shorter than rods. Nrl-/- photoreceptors express the mouse UV cone pigment, cone transducin, and cone arrestin in amounts expected, given the relative size and density of cones in the two retinas. The ERG a-wave was used to assay the properties of the photocurrent response. The sensitivity of the Nrl -/- a-wave is at its maximum at 360 run, with a secondary mode at 510 nm having approximately one-tenth the maximum sensitivity. These wavelengths are the λmax of the two mouse cone pigments. The time to peak of the dim-flash photocurrent response was ∼50 ms, more than two times faster than that of rods. CONCLUSIONS. Many morphological, molecular, and electrophysiological features of the Nrl-/- photoreceptors are cone-like, and strongly distinguish these cells from rods. This retina provides a model for the investigation of cone function and cone-specific genetic disease.

AB - PURPOSE. To test the hypothesis that Nrl-/- photoreceptors are cones, by comparing them with WT rods and cones using morphological, molecular, histochemical, and electrophysiological criteria. METHODS. The photoreceptor layer of fixed retinal tissue of 4- to 6-week-old mice was examined in plastic sections by electron microscopy, and by confocal microscopy in frozen sections immunolabeled for the mouse UV-cone pigment and colabeled with PNA. Quantitative immunoblot analysis was used to determine the levels of expression of key cone-specific proteins. Single- and paired-flash methods were used to extract the spectral sensitivity, kinetics, and amplification of the a-wave of the ERG. RESULTS. Outer segments of Nrl-/- photoreceptors (∼7 μm) are shorter than those of wild-type (WT) rods (∼25 μm) and cones (∼15 μm); but, like WT cones, they have 25 or more basal discs open to the extracellular space, extracellular matrix sheaths stained by PNA, chromatin "clumping" in their nuclei, and mitochondria two times shorter than rods. Nrl-/- photoreceptors express the mouse UV cone pigment, cone transducin, and cone arrestin in amounts expected, given the relative size and density of cones in the two retinas. The ERG a-wave was used to assay the properties of the photocurrent response. The sensitivity of the Nrl -/- a-wave is at its maximum at 360 run, with a secondary mode at 510 nm having approximately one-tenth the maximum sensitivity. These wavelengths are the λmax of the two mouse cone pigments. The time to peak of the dim-flash photocurrent response was ∼50 ms, more than two times faster than that of rods. CONCLUSIONS. Many morphological, molecular, and electrophysiological features of the Nrl-/- photoreceptors are cone-like, and strongly distinguish these cells from rods. This retina provides a model for the investigation of cone function and cone-specific genetic disease.

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