MODULATING BONE MORPHOGENIC PROTEIN (BMP) SIGNALING IN THE TREATMENT OF ALZHEIMER'S DISEASE
Methods and compositions are provided for the treatment of Alzheimer's Disease (AD) by administering to a patient a therapeutically effective amount of an agent that inhibits signaling mediated by a bone morphogenetic protein type 1A receptor (BMPR-1A) or bone morphogenetic protein type 2 receptor (BMPR-2). Also provided are methods and compositions to increase the rate of neural stem cell self-renewal.
1 . A method of treating a subject having Alzheimer's Disease (AD), the method comprising administering to the subject a therapeutically effective amount of an agent that inhibits signaling by BMPR-1A, BMPR-2, or both BMPR-1A and BMPR-2.
2 . A method of increasing the rate of self-renewal of a stem cell, the method comprising contacting the stem cell with an agent that inhibits signaling by BMPR-1A, BMPR-2, or both BMPR-1A and BMPR-2.
3 . The method of claim 1 , which is a method of increasing the rate of neural stem cell self-renewal in the subject.
4 . The method of claim 1 , wherein the agent:
(a) inhibits expression of a BMPR-1A mRNA or protein;
(b) binds a BMPR-1A protein; and/or
(c) inhibits interaction between a BMP protein and a BMPR-1A.
5 . The method of claim 1 , wherein the agent:
(a) inhibits expression of a BMPR-2 mRNA or protein;
(b) binds a BMPR-2 protein; and/or
(c) inhibits interaction between a BMP protein and a BMPR-2.
6 . The method of claim 1 , wherein the agent is a nucleic acid.
7 . The method of claim 6 , wherein the agent is a small interfering RNA (siRNA) or a short hairpin RNA (shRNA) that targets BMPR-1A, BMPR-2A, or both BMPR-1A and BMPR-2.
8 . The method of claim 6 , wherein the agent is an antisense oligonucleotide (ASO) that targets BMPR-1A, BMPR-2A, or both BMPR-1A and BMPR-2.
9 . The method of claim 6 , wherein the agent is a guide RNA (gRNA).
10 . The method of claim 1 , wherein the agent is a protein or an aptamer.
11 . The method of claim 10 , wherein the agent is an antibody.
12 . The method of claim 11 , wherein the agent is a blocking or neutralizing antibody that binds specifically to BMPR-1A, BMPR-2A, or both BMPR-1A and BMPR-2.
13 . The method of claim 2 , wherein the stem cell is a neural stem cell or a neural progenitor cell.
14 . A method of preparing a medicament for treating Alzheimer's Disease (AD) or increasing neural stem cell self-renewal in a subject in need thereof, the method comprising:
identifying a compound that is effective as an agent to inhibit signaling by BMPR-1A, BMPR-2, or both BMPR-1A and BMPR-2 on neural stem cells, and
compounding a therapeutically effective amount of the compound with a pharmaceutically acceptable excipient so as to produce the medicament.
15 . The method of claim 14 , wherein the agent:
(a) inhibits expression of a BMPR-1A mRNA or protein;
(b) binds a BMPR-1A protein; and/or
(c) inhibits interaction between a BMP protein and a BMPR-1A.
16 . The method of claim 14 , wherein the agent:
(a) inhibits expression of a BMPR-2 mRNA or protein;
(b) binds a BMPR-2 protein; and/or
(c) inhibits interaction between a BMP protein and a BMPR-2.
17 . The method of claim 14 , wherein the agent is a nucleic acid selected from a small interfering RNA (siRNA), a short hairpin RNA (shRNA), an antisense oligonucleotide (ASO) and a guide RNA (gRNA), wherein the nucleic acid targets BMPR-1A, BMPR-2A, or both BMPR-1A and BMPR-2.
18 . The method of claim 14 , wherein the agent is a blocking or neutralizing antibody that binds specifically to BMPR-1A, BMPR-2A, or both BMPR-1A and BMPR-2.
19 . A unit dose of a medicament prepared according to the method of claim 14 , wherein formulation of the medicament and the amount of the agent contained in the unit dose are selected such that the unit dose is effective in treating Alzheimer's Disease (AD) in a subject in need thereof.
20 . A unit dose of a medicament prepared according to the method of claim 14 , wherein formulation of the medicament and the amount of the agent contained in the unit dose are selected such that the unit dose is effective in increasing the rate of neural stem cell self-renewal in a subject in need thereof.