High-throughput screening assay for cholesterol inhibitors and inhibitors identified thereby
The present invention provides a high-throughput screening assay to identify test agents as cholesterol inhibitors via mutant NCP1 mammalian cells. Also provided are cholesterol inhibiting agents identified in accordance with this assay and methods for using such agents to inhibit cholesterol accumulation in cells.
1. A high-throughput screening assay for identification of cholesterol inhibitors comprising exposing mutant NPC1 mammalian cells to a test agent, measuring a sterol efflux level in media of the mutant NPC1 mammalian cells exposed to the test agent, and comparing the measured level to a sterol efflux level in mutant NPC1 cells not exposed to the test agent, wherein an increase in the measured sterol efflux level in the mutant NPC1 cells exposed to the test agent as compared to the level in mutant NPC1 cells not exposed to the test agent is indicative of the test agent being a cholesterol inhibitor.
2. The method of claim 1 wherein the mutant NPC1 cells comprise CHO CT43 or CT60 cells.
3. The method of claim 1 wherein sterol efflux levels are measured via a pulse chase protocol.
4. A high-throughput screening assay for identification of cholesterol inhibitors comprising exposing mutant NPC1 mammalian cells to a test agent, measuring a sterol efflux level in media of the mutant NPC1 mammalian cells exposed to the test agent, and comparing the measured level to a sterol efflux level in parenteral cells not exposed to the test agent, wherein a measured sterol efflux level in the mutant NPC1 cells exposed to the test agent equal to the sterol efflux level in parenteral cells test agent is indicative of the test agent being a cholesterol inhibitor.
5. The method of claim 1 wherein the mutant NPC1 cells comprise CHO CT43 or CT60 cells and the parenteral cells comprise CHO 25RA cells.
6. The method of claim 4 wherein sterol efflux levels are measured via a pulse chase protocol.