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Phospholipid phosphatase-related protein type 5 (PLPPR5) is a membrane protein belonging to the phospholipid phosphatase-related (PLPPR) family, characterized by six transmembrane domains and evolutionary relation to phosphatidic acid phosphatases. It is predominantly expressed in the nervous system—especially in dendritic compartments postnatally—and is involved in promoting the formation of filopodia, neurite outgrowth, and dendritic spines. PLPPR5 acts independently of canonical CDC42/formin-mediated pathways and can reduce lysophosphatidic acid (LPA)-induced RhoA/ROCK signaling, thereby antagonizing neurite retraction. Mutations or altered expression are associated with specific neurodevelopmental syndromes such as Barre-Lieou syndrome and Bardet-Biedl syndrome 10. Currently, PLPPR5 is not directly targeted by any approved drugs but may be implicated in future research on neural repair, regeneration, or plasticity-related disorders.
Not currently targeted by drugs; overexpression studies implicate alteration of cytoskeletal and signaling pathways; possible modulation of Rho/ROCK pathway
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