Determining the effect of a substance on sequestration, uptake, and accumulation of amyloid in brain cells
View Patent ↗The present invention provides brain cells, such as normal brain cells, apolipoprotein E deficient brain cells, or apoE4 containing brain cells, that are treated with a compound which can modulate integrins and/or integrin receptors to produce increased sequestration of and/or accumulation of and/or uptake of Aβ, and/or changes in cathepsin D content and/or lysosomal dysfunction, and/or microglia activation in the brain cells. The present invention also provides methods for producing such cells and methods for using the cells for screening an agent or substance that modulates the sequestration of and/or accumulation of and/or uptake of Aβ, and/or lysosomal dysfunction, and/or changes in cathepsin D content and/or microglia activation in the brain cells. The method further provides a new therapeutic target, antagonism of glutamate receptors, for the treatment of neurodegenerative diseases which are characterized by inter alia, abnormal amyloid uptake and/or accumulation.
1. A method for determining the effect of a substance on sequestration, uptake or accumulation of amyloid in brain cells, said method comprising:
(A) exposing brain cells in vitro to an integrin antagonist, wherein said antagonist is selected from the group consisting of function blocking anti-β5 subunit integrin antibody, function blocking anti-β1 subunit integrin antibody, an RGD peptide capable of modifying integrin adhesion, RGDS peptide, GRGDS peptide, GRGDSP peptide, GRGDTP peptide and echistatin,
(B) maintaining said cells for a time sufficient to induce sequestration, uptake or accumulation of amyloid in said cells as a result of said antagonist,
(C) adding said substance before, during and/or after said exposing or maintaining; and
(D) determining whether the presence of said substance has an effect on said antagonist induced sequestration, uptake or accumulation of amyloid.
2. The method of claim 1 , wherein sequestration, uptake or accumulation of amyloid increases.
3. The method of claim 2 , wherein said increase is at least about 10% compared to a control.
4. The method of claim 1 , wherein at least one of said sequestration, uptake or accumulation of amyloid decreases.
5. The method of claim 4 , wherein said decrease is at least about 10% compared to a control.
6. The method of claim 1 , wherein the brain cells are in the form of a brain slice.
7. The method of claim 6 , wherein the brain slice is a hippocampal slice, an entorhinal cortex slice, an entorhinohippocampal slice, a neocortex slice, a hypothalamic slice, or a cortex slice.
8. The method of claim 1 , wherein said antagonist is said function blocking anti-α5 subunit integrin antibody or said function blocking anti-β1 subunit integrin antibody.
9. The method of claim 1 , wherein said antagonist is said RGD peptide, RGDS peptide, GRGDS peptide, GRGDTP peptide, GRGDSP peptide or echistatin.
10. The method of claim 1 , wherein the amount of sequestration of amyloid, accumulation of amyloid, or uptake of amyloid, is determined visually.
11. The method of claim 1 , wherein the amount of sequestration of amyloid, accumulation of amyloid, or uptake of amyloid is measured using a capture reagent.
12. The method of claim 10 , wherein the capture reagent is an antibody that binds to amyloid.
13. The method of claim 1 wherein said cells are apolipoprotein E deficient brain cells or apolipoprotein E4 containing brain cells cultured in a medium which selectively increases sequestration of and/or accumulation of and/or uptake of amyloid, and/or lysosomal dysfunction, and/or microglia activation in the brain cells, wherein the brain cells comprise an increased amount of sequestration of and/or accumulation of and/or uptake of amyloid, and/or lysosomal dysfunction, and/or microglia activation compared to a control.
14. The method of claim 1 wherein said substance is added prior to exposing said brain cells to said antagonist.
15. The method of claim 1 , wherein said substance is added to said brain cells simultaneously with said antagonist.
16. A method for determining whether a substance is capable of inhibiting sequestration, uptake or accumulation of amyloid in brain cells, said method comprising:
(A) exposing brain cells in vitro to an integrin antagonist, wherein said antagonist is selected from the group consisting of function blocking anti-α5 subunit integrin antibody, function blocking anti-β1 subunit integrin antibody, an RGD peptide capable of modifying integrin adhesion, RGDS peptide, GRGDS peptide, GRGDSP peptide, GRGDTP peptide and echistatin,
(B) maintaining said cells for a time sufficient to induce sequestration, uptake or accumulation of amyloid one or more characteristics of a neurodegenerative disease in said cells as a result of said antagonist,
(C) adding said substance before, during and/or after said exposing or maintaining; and
(D) determining whether the presence of said substance inhibits one or more of said characteristics sequestration, uptake or accumulation of amyloid in said cells.
17. The method of claim 16 , wherein at least one of said sequestration, uptake or accumulation of amyloid decreases.
18. The method of claim 17 , wherein said decrease is at least about 10% compared to a control.
19. The method of claim 16 , wherein the brain cells are in the form of a brain slice.
20. The method of claim 19 , wherein the brain slice is a hippocampal slice, an entorhinal cortex slice, an entorhinohippocampal slice, a neocortex slice, a hypothalamic slice, or a cortex slice.
21. The method of claim 16 , wherein said antagonist is said function blocking anti-α5 subunit integrin antibody or said function blocking anti-β3 subunit integrin antibody.
22. The method of claim 16 , wherein said antagonist is said RGD peptide, RGDS peptide, GRGDS peptide, GRGDTP peptide, GRGDSP peptide or echistatin.
23. The method of claim 16 , wherein the amount of sequestration of amyloid, accumulation of amyloid, or uptake of amyloid is determined visually.
24. The method of claim 16 , wherein the amount of sequestration of amyloid, accumulation of amyloid, or uptake of amyloid is measured using a capture reagent.
25. The method of claim 24 , wherein the capture reagent is an antibody that binds to amyloid.
26. The method of claim 16 wherein said cells are apolipoprotein E deficient brain cells or apolipoprotein E4 containing brain cells.