Inhibition of the β3 subunit of L-type Ca
View Patent ↗The present invention provides reagents and methods for identifying inhibitors of the L-type Ca 2+ channel β 3 protein, which has been demonstrated to be involved in calcium signaling, insulin secretion, and glucose homeostasis. The invention also provides therapeutics and methods for treating a subject with one or more of diabetes, insulin resistance, impaired insulin secretion, and impaired glucose homeostasis, involving the use of inhibitors of an L-type Ca 2+ channel β 3 subunit to provide a benefit to the subject.
1. A method for identifying inhibitors of the L-type Ca 2+ channel β 3 protein, comprising:
a) contacting recombinant host cells with a calcium indicator that emits detectable signals in the presence of calcium, wherein the recombinant host cells have been transfected with a recombinant expression vector comprising nucleic acid control sequences operatively linked to an L-type Ca 2+ channel β 3 protein-encoding nucleic acid sequence, wherein the contacting occurs under conditions to promote expression of the L-type Ca 2+ channel β 3 protein and wherein the host cell does not possess functional β 3 protein-containing L-type Ca 2+ channels after expression of the L-type Ca 2+ channel β 3 protein;
b) treating the host cells with one or more test compounds, wherein the treating occurs before, simultaneous with, or after the contacting of the host cells with the calcium indicator;
c) stimulating the recombinant host cells with an amount of ATP that is effective to increase intracellular calcium concentration release from cellular stores; and
d) detecting signals from the calcium indicator in the recombinant host cells, wherein a test compound-induced increase in the signals from the calcium indicator in the recombinant host cells as compared to a control indicates that the test compound promotes release of calcium from intracellular stores, and wherein the test compound is an inhibitor of the L-type Ca 2+ channel β 3 protein.
2. The method of claim 1 , wherein the method is used to identify compounds for use in treating one or more disorders selected from the group consisting of diabetes, insulin resistance, impaired insulin secretion, and impaired glucose homeostasis.
3. The method of claim 1 wherein the recombinant host cells are mammalian cells.
4. The method of claim 3 wherein the recombinant host cells are human cells.
5. The method of claim 1 wherein the L-type Ca 2+ channel β 3 protein-encoding nucleic acid sequence encodes the protein of SEQ ID NO:6.
6. The method of claim 5 , wherein the recombinant host cells are human cells.
7. The method of claim 6 , wherein the method is used to identify compounds for use in treating one or more disorders selected from the group consisting of diabetes, insulin resistance, impaired insulin secretion, and impaired glucose homeostasis.
8. The method of claim 6 , wherein step (c) comprises stimulating the recombinant host cells with between 1 μM and 100 μM ATP.