Expression of foxp3 in edited cd34+ cells
US-2024117352-A1 · Apr 11, 2024 · US
US2016333316A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016333316-A1 |
| Application number | US-201515110004-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 9, 2015 |
| Priority date | Jan 9, 2014 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
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The present invention provides a method of inducing microglia cells from blood cells, comprising culturing the blood cells in the presence of interleukin-34 (IL-34) and granulocyte-macrophage colony stimulating factor (GM-CSF).
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1 . A method of inducing microglial cells from blood cells, comprising culturing the blood cells in the presence of interleukin-34 (IL-34) and granulocyte-macrophage colony stimulating factor (GM-CSF). 2 . A method of producing microglial cells, comprising culturing blood cells in the presence of interleukin-34 (IL-34) and granulocyte-macrophage colony stimulating factor (GM-CSF), and collecting microglial cells from the culture. 3 . The method of claim 1 or 2 , wherein the blood cells are human peripheral monocytes. 4 . The method of claim 1 or 2 , wherein a concentration of IL-34 is 1-200 ng/ml. 5 . The method of claim 1 or 2 , wherein a concentration of GM-CSF is 1-200 ng/ml. 6 . A microglial cell obtained by the method claim 1 . 7 . A kit for inducing microglial cells from blood cells, comprising interleukin-34 (IL-34) and granulocyte-macrophage colony stimulating factor (GM-CSF). 8 . A method of screening a therapeutic drug for a psychiatric disease or a neurodegenerative disease, comprising the steps of: causing the microglial cell according to claim 6 to make contact with a candidate substance to measure a cellular activity of the cell; and using the obtained measurement result as an indicator. 9 . The method according to claim 8 , wherein the cellular activity is at least one selected from the group consisting of phagocytosis, proliferation capacity, viability, neurite elongation capability, cytokine production, morphological changes and differentiation capacity. 10 . The method according to claim 8 or 9 , wherein the psychiatric disease or neurodegenerative disease is at least one selected from the group consisting of schizophrenia, mood disorder, dementia, autism, amyotrophic lateral sclerosis (ALS), Parkinson's disease, Huntington's chorea, prion diseases, multiple sclerosis, and physical diseases. 11 . The method according to claim 10 , wherein the physical diseases are autoimmune disorders, atopic disorders or diabetes. 12 . A method of evaluating a responsiveness of a therapeutic drug for a psychiatric disease or a neurodegenerative disease, comprising the steps of: causing the microglial cell according to claim 6 to make contact with a candidate substance to measure a cellular activity of the cell; and using the obtained measurement result as an indicator. 13 . The method according to claim 11 , wherein the cellular activity is at least one selected from the group consisting of phagocytosis, proliferation capacity, viability, neurite elongation capability, cytokine production, morphological changes and differentiation capacity. 14 . The method according to claim 12 , wherein the psychiatric disease or neurodegenerative disease is at least one selected from the group consisting of schizophrenia, mood disorder, dementia, autism, amyotrophic lateral sclerosis (ALS), Parkinson's disease, Huntington's chorea, prion diseases, multiple sclerosis, and physical diseases. 15 . A kit for screening or evaluating a therapeutic drug for a psychiatric disease or a neurodegenerative disease, comprising a microglial cell according to claim 6 . 16 . A pharmaceutical composition for treating a psychiatric disease or a neurodegenerative disease, comprising a microglial cell according to claim 6 .
Anti-Parkinson drugs · CPC title
Drugs for disorders of the nervous system · CPC title
Neurological disorders · CPC title
from monocytes, from macrophages · CPC title
Psychoses; Psychiatry · CPC title
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