Abstract:Background: Pronounced asymmetric changes in ocular globe size during eye development have been observed in a number of species ranging from humans to lizards. In contrast, largely symmetric changes in globe size have been described for other species such as rodents. We propose that asymmetric changes in the three-dimensional structure of the developing eye correlate with the types of retinal remodeling needed to produce areas of high photoreceptor density. As a test of this idea, we systematically examined th… Show more
“…2 of Rasys et al (2021b)). By late stage 3, an increase in the number of cells dividing in the central region of the retina is observed, and by stage 4, a slight mounding to the retina (i.e., increased neural retina thickness) is detected centrally (data not shown; see Anolis Eye Development poster from Rasys et al (2021a)). As the embryo enters stage 5 of development, the eye has grown considerably in overall size and regional differences in both morphology and the relative numbers of mitotic figures become clearly evident (Fig.…”
Section: Cell Proliferation and Retina Laminationmentioning
confidence: 91%
“…This change in length is accompanied by a regional decrease in the cellular density of the neural retina, which is noticeable as a thinning of the GCL (Rasys et al, 2021a). By stage 15 the ocular globe begins to retract, concomitant with regional increases in cellular density (Rasys et al, 2021a). By the time of hatching, the GCL is 4-6 cells deep in all retinal regions except that of the central fovea, which is devoid of ganglion cells due to lateral displacement (Fig.…”
Section: Neurogenesis Of Retina Cell-typesmentioning
confidence: 98%
“…We began by looking at the development of the foveae of the retina. Formation of the foveae occur during the last week of embryonic development in anoles, between stages 16-18; it is during this time period that the eye is actively undergoing ocular retraction (Rasys et al, 2021a). As the foveae form, they do so through the lateral displacement of the retina nuclear layers and the movement of photoceptor cells towards the foveal centers.…”
Section: Fovea Formation and Retinal Remodelingmentioning
confidence: 99%
“…Anole embryos develop over a 30-33 day period when incubated at 28˚C. Embryos were collected from eggs at various timepoints after egg lay and removed from their egg shells following the protocol described by Rasys et al (2021a) and staged according to Sanger et al, 2008guidelines (Sanger et al, 2008b. Eyes were collected from 4 plus embryos from each developmental stage.…”
Section: Staging and Dissectionmentioning
confidence: 99%
“…Therefore, we are developing the brown anole lizard (Anolis sagrei) as a foveated model system for research (Rasys et al, 2021a, Rasys et al, 2019a, Rasys et al, 2019b, Rasys et al, 2021b. This lizard has a bifoveated retina, possessing a large prominent central fovea and second, much shallower, temporal fovea (Rasys et al, 2021a, Fite and Lister, 1981, Makaretz and Levine, 1980, Sannan et al, 2018, Underwood, 1970, Walls, 1942. Remarkably, during embryonic development anole eyes undergo dynamic changes in their ocular shape (Rasys et al, 2021a).…”
Background. The fovea, a pit in the retina, is believed to be important for high-acuity vision and is a feature found in the eyes of humans and a limited number of vertebrate species that include certain primates, birds, lizards, and fish. At present, model systems currently used for ocular research lack a foveated retina and studies investigating fovea development have largely been limited to histological and molecular studies in primates. As a result, progress towards understanding the mechanisms involved in regulating fovea development in humans is limited and is completely lacking in other, non-primate, vertebrates. To address this knowledge gap, we provide here a detailed histological atlas of retina and fovea development in the bifoveated Anolis sagrei lizard, a novel reptile model for fovea research. We also further test the hypothesis that retinal remodeling, which leads to fovea formation and photoreceptor cell packing, is related to asymmetric changes in eye shape.
Results. Anole retina development follows the conventional spatiotemporal patterning observed in most vertebrates, where retina neurogenesis begins within the central retina, progresses throughout the temporal retina, and concludes in the nasal retina. One exception to this general rule is that areas that give rise to the fovea undergo retina differentiation prior to the rest of the retina. We find that retina thickness changes dynamically during periods of ocular elongation and retraction. During periods of ocular elongation, the retina thins, while during retraction it becomes thicker. Ganglion cell layer mounding is also observed in the temporal fovea region just prior to pit formation.
Conclusions. Anole retina development parallels that of humans, including the onset and progression of retinal neurogenesis followed by changes in ocular shape and retinal remodeling that leads to pit formation in the retina. We propose that anoles are an excellent model system for fovea development research.
“…2 of Rasys et al (2021b)). By late stage 3, an increase in the number of cells dividing in the central region of the retina is observed, and by stage 4, a slight mounding to the retina (i.e., increased neural retina thickness) is detected centrally (data not shown; see Anolis Eye Development poster from Rasys et al (2021a)). As the embryo enters stage 5 of development, the eye has grown considerably in overall size and regional differences in both morphology and the relative numbers of mitotic figures become clearly evident (Fig.…”
Section: Cell Proliferation and Retina Laminationmentioning
confidence: 91%
“…This change in length is accompanied by a regional decrease in the cellular density of the neural retina, which is noticeable as a thinning of the GCL (Rasys et al, 2021a). By stage 15 the ocular globe begins to retract, concomitant with regional increases in cellular density (Rasys et al, 2021a). By the time of hatching, the GCL is 4-6 cells deep in all retinal regions except that of the central fovea, which is devoid of ganglion cells due to lateral displacement (Fig.…”
Section: Neurogenesis Of Retina Cell-typesmentioning
confidence: 98%
“…We began by looking at the development of the foveae of the retina. Formation of the foveae occur during the last week of embryonic development in anoles, between stages 16-18; it is during this time period that the eye is actively undergoing ocular retraction (Rasys et al, 2021a). As the foveae form, they do so through the lateral displacement of the retina nuclear layers and the movement of photoceptor cells towards the foveal centers.…”
Section: Fovea Formation and Retinal Remodelingmentioning
confidence: 99%
“…Anole embryos develop over a 30-33 day period when incubated at 28˚C. Embryos were collected from eggs at various timepoints after egg lay and removed from their egg shells following the protocol described by Rasys et al (2021a) and staged according to Sanger et al, 2008guidelines (Sanger et al, 2008b. Eyes were collected from 4 plus embryos from each developmental stage.…”
Section: Staging and Dissectionmentioning
confidence: 99%
“…Therefore, we are developing the brown anole lizard (Anolis sagrei) as a foveated model system for research (Rasys et al, 2021a, Rasys et al, 2019a, Rasys et al, 2019b, Rasys et al, 2021b. This lizard has a bifoveated retina, possessing a large prominent central fovea and second, much shallower, temporal fovea (Rasys et al, 2021a, Fite and Lister, 1981, Makaretz and Levine, 1980, Sannan et al, 2018, Underwood, 1970, Walls, 1942. Remarkably, during embryonic development anole eyes undergo dynamic changes in their ocular shape (Rasys et al, 2021a).…”
Background. The fovea, a pit in the retina, is believed to be important for high-acuity vision and is a feature found in the eyes of humans and a limited number of vertebrate species that include certain primates, birds, lizards, and fish. At present, model systems currently used for ocular research lack a foveated retina and studies investigating fovea development have largely been limited to histological and molecular studies in primates. As a result, progress towards understanding the mechanisms involved in regulating fovea development in humans is limited and is completely lacking in other, non-primate, vertebrates. To address this knowledge gap, we provide here a detailed histological atlas of retina and fovea development in the bifoveated Anolis sagrei lizard, a novel reptile model for fovea research. We also further test the hypothesis that retinal remodeling, which leads to fovea formation and photoreceptor cell packing, is related to asymmetric changes in eye shape.
Results. Anole retina development follows the conventional spatiotemporal patterning observed in most vertebrates, where retina neurogenesis begins within the central retina, progresses throughout the temporal retina, and concludes in the nasal retina. One exception to this general rule is that areas that give rise to the fovea undergo retina differentiation prior to the rest of the retina. We find that retina thickness changes dynamically during periods of ocular elongation and retraction. During periods of ocular elongation, the retina thins, while during retraction it becomes thicker. Ganglion cell layer mounding is also observed in the temporal fovea region just prior to pit formation.
Conclusions. Anole retina development parallels that of humans, including the onset and progression of retinal neurogenesis followed by changes in ocular shape and retinal remodeling that leads to pit formation in the retina. We propose that anoles are an excellent model system for fovea development research.
Positive allometry of signalling traits has often been taken as evidence for sexual selection. However, few studies have explored interspecific differences in allometric scaling relationships among closely related species that vary in their degree of ecological similarity.
Anolis
lizards possess an elaborate retractable throat fan called a dewlap that is used for visual communication and differs greatly in size and colour among species. We observed that
Anolis
dewlaps demonstrate positive allometry: relative dewlap size increases with body size. We also observed that coexisting species are divergent in signal size allometries, while convergent species—similar in other aspects of ecology, morphology and behaviour—typically share similar dewlap allometric scaling relationships. These patterns suggest that dewlap scaling relationships may follow the same pattern as other traits in the anole radiation, where ecologically different sympatric species have evolved a suite of divergent traits.
Background: Anterior eye development has been explored in different vertebrate species ranging from fish to mammals. However, missing from this diverse group is a representative of reptiles. A promising candidate to fill this void is the brown anole, Anolis sagrei, which is easily raised in the laboratory and for which genome editing techniques exist. Here we provide a detailed histological analysis of the development of the anterior structures of the eye in A. sagrei, which include the cornea, iris, ciliary body, lens, trabecular meshwork, and sclera ossicles.
Results: Development of the anterior segment in Anoles proceeds as for other vertebrates with the lens forming first followed by the cornea, then the iris, ciliary body, trabecular meshwork, and sclera ossicles. The onset of these latter structures occurs first temporally than nasally. Unlike the eyes of mammals and birds, anoles possess a remarkably thin cornea, flat ciliary body, and a trabecular meshwork that lacks an obvious Schlemm's canal.
Conclusions: This study highlights several features present in anoles and represents an important step towards understanding reptile eye development.
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