Arap1 Loss Causes RPE Phagocytic Dysfunction and Subsequent Photoreceptor Death

Shao, A.; Jacobo Lopez, A.; Chen, J.; Tham, A.; Javier, S.; Quiroz, A.; Frick, S.; Levine, E. M.; Lloyd, K. C. K.; Leonard, B. C.; Murphy, C. J.; Glaser, T. M.; Moshiri, A.

doi:10.1101/2021.08.09.455745

bioRxiv · 10.1101/2021.08.09.455745

Arap1 Loss Causes RPE Phagocytic Dysfunction and Subsequent Photoreceptor Death

Shao, A.·Jacobo Lopez, A.·Chen, J.·Tham, A.·Javier, S.·Quiroz, A.·Frick, S.·Levine, E. M.·Lloyd, K. C. K.·Leonard, B. C.·Murphy, C. J.·Glaser, T. M.·Moshiri, A.

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Abstract

PurposeArap1 is an Arf-directed GTPase-activating protein (GAP) shown to modulate actin cytoskeletal dynamics by regulating Arf and Rho family members. We have previously shown that Arap1-/- mice develop photoreceptor degeneration similar to the human condition retinitis pigmentosa (RP), corroborated by fundus examination, histopathology, and ERG analysis. However, Arap1 expression was not detected in photoreceptors, but in Muller Glia and retinal pigment epithelium (RPE), suggesting a non-cell-autonomous mechanism for degeneration. The aim of this study was to elucidate the role of retinal Arap1 in photoreceptor maintenance. MethodsAlbino Arap1-/- mice were generated via breeding pigmented Arap1-/- mice onto a Tyr-/- C57BL/6J background. Conditional knockout (cKO) mice were generated for Muller Glia/RPE, Muller Glia, and RPE via targeting Cralbp, Glast, and Vmd2 promoters, respectively, to drive Cre recombinase expression to knock out Arap1. Mice were analyzed by fundus photography, optical coherence tomography (OCT), histology, and immunohistochemistry. Arap1 binding partners were assayed by affinity purification mass spectrometry. ResultsVmd2-Cre Arap1tm1c/tm1c and Cralbp-Cre Arap1tm1c/tm1c mice, but not Glast-Cre Arap1tm1c/tm1c mice, recapitulated the photoreceptor degeneration phenotype originally observed in germline Arap1-/- mice. These findings were corroborated by fundus exam, OCT, and histological analysis. Mass spectrometry analysis of ARAP1 co-immunoprecipitation identified putative binding partners of ARAP1, revealing numerous interactants involved in phagocytosis, cytoskeletal composition, intracellular trafficking, and endocytosis. Quantification of rod outer segment (OS) phagocytosis in vivo demonstrated a clear phagocytic defect in Arap1-/- mice compared to Arap1+/+ littermate controls while cone phagocytosis was preserved. ConclusionsArap1 expression, specifically in RPE, is necessary for photoreceptor survival due to its indispensable function in RPE phagocytosis. We propose a model in which Arap1 regulates G-protein function for nonmuscle myosin II targeting during phagocytosis. This novel role of Arap1 is important for further understanding of both the diversity of its functions and the complex molecular regulation of RPE phagocytosis.

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Shao, A., Jacobo Lopez, A., Chen, J., Tham, A., Javier, S., Quiroz, A., Frick, S., Levine, E. M., Lloyd, K. C. K., Leonard, B. C., Murphy, C. J., Glaser, T. M., Moshiri, A.. 2021-08-10. Arap1 Loss Causes RPE Phagocytic Dysfunction and Subsequent Photoreceptor Death. https://doi.org/10.1101/2021.08.09.455745

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