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公开(公告)号:US20180080009A1
公开(公告)日:2018-03-22
申请号:US15558473
申请日:2016-03-17
发明人: Hideyuki OKANO , Seiji SHIOZAWA , Fumihiko KISA
IPC分类号: C12N5/074
CPC分类号: C12N5/0696 , C12N5/10 , C12N15/09 , C12N2501/01 , C12N2501/20 , C12N2501/60 , C12N2501/602 , C12N2501/603 , C12N2501/605 , C12N2501/606
摘要: To produce and/or maintain naïve pluripotent stem cells capable of highly expressing genes important for maintaining an undifferentiated state, which could not be achieved by known methods for producing pluripotent stem cells. The present invention can produce naïve pluripotent stem cells capable of maintaining an undifferentiated state by introducing and allowing transient expression of six genes (Oct3/4, Klf4, c-Myc, Sox2, Nanog, and Klf2) among the so-called initializing factors, and further performing culturing in a medium containing LIF, an MEK inhibitor, a GSK3 inhibitor, a cAMP production promoter, a TGF-β inhibitor and a PKC inhibitor. Thus, the problem of the present invention can be solved.
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公开(公告)号:US20200325453A1
公开(公告)日:2020-10-15
申请号:US16917464
申请日:2020-06-30
发明人: Hideyuki OKANO , Seiji Shiozawa , Fumihiko Kisa
摘要: To produce and/or maintain naïve pluripotent stem cells capable of highly expressing genes important for maintaining an undifferentiated state, which could not be achieved by known methods for producing pluripotent stem cells. The present invention can produce naïve pluripotent stem cells capable of maintaining an undifferentiated state by introducing and allowing transient expression of six genes (Oct3/4, Klf4, c-Myc, Sox2, Nanog, and Klf2) among the so-called initializing factors, and further performing culturing in a medium containing LIF, an MEK inhibitor, a GSK3 inhibitor, a cAMP production promoter, a TGF-β inhibitor and a PKC inhibitor. Thus, the problem of the present invention can be solved.
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公开(公告)号:US20230203439A1
公开(公告)日:2023-06-29
申请号:US18116415
申请日:2023-03-02
申请人: JSR Corporation , KEIO UNIVERSITY
发明人: Mitsuru ISHIKAWA , Hideyuki OKANO
CPC分类号: C12N5/0622 , C12N15/86 , C12N2501/60 , C12N2506/45 , C12N2740/15043
摘要: A method is provided for producing oligodendrocyte-like cells, including (A) increasing abundances of oligodendrocyte transcription factor 2 (OLIG2) mutant and SRY-box transcription factor 10 (SOX10) in human pluripotent stein cells and (B) culturing the human pluripotent stem cells in which the abundances of the OLIG2 mutant and the SOX10 are increased and consequently differentiating the human pluripotent stem cells into oligodendrocyte-like cells, in which the OLIG2 mutant lacks a serine residue of wild-type OLIG2 at position 147, or the serine residue of the wild-type OLIG2 at position 147 is substituted with an amino acid other than serine.
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公开(公告)号:US20240279605A1
公开(公告)日:2024-08-22
申请号:US18648566
申请日:2024-04-29
申请人: JSR CORPORATION , KEIO UNIVERSITY
IPC分类号: C12N5/0793
CPC分类号: C12N5/0619 , C12N2500/36 , C12N2501/13 , C12N2513/00
摘要: A culture method includes culturing a spheroid of a human neural cell-like cell in the presence of a tau protein aggregate and culturing a culture product in a culture medium containing 5 μg/mL or greater of a lipid, in which the lipid is one or more selected from the group consisting of a glycerolipid, a glycerophospholipid, and a sphingolipid. The culture method includes culturing a spheroid of a human neural cell-like cell in the presence of a tau protein aggregate and culturing a culture product in a culture medium containing a neurotrophic factor.
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公开(公告)号:US20240252546A1
公开(公告)日:2024-08-01
申请号:US18561077
申请日:2022-05-27
申请人: KEIO UNIVERSITY
发明人: Hideyuki OKANO , Yoshitaka KASE
IPC分类号: A61K35/30 , C12N5/0793 , G01N33/50
CPC分类号: A61K35/30 , C12N5/0619 , G01N33/5058 , C12N2501/734 , C12N2503/00 , C12N2506/45
摘要: A neurite outgrowth promotion kit containing a γ-secretase inhibitor or a GADD45G expression vector, in which the neurite outgrowth promotion kit is used for significantly promoting neurite outgrowth of nerve cells as compared with a control, by acting on a neurosphere to induce differentiation of the neurosphere into nerve cells; a method for producing a neurosphere for treatment of spinal cord injury, which includes a step of using the above-described neurite outgrowth promotion kit on a neurosphere derived from a pluripotent stem cell; a neurosphere for treatment of spinal cord injury; and a method for selecting a neurosphere for treatment of spinal cord injury and a method for screening a neurite outgrowth-promoting agent.
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公开(公告)号:US20220326225A1
公开(公告)日:2022-10-13
申请号:US17709903
申请日:2022-03-31
发明人: Hirokazu TANABE , Setsu ENDOH , Hitoshi MASUYAMA , Euikyung SHIN , Koichi SAITO , Hideyuki OKANO , Sumihiro MAEDA
IPC分类号: G01N33/50 , C12Q1/6897 , C12N5/0793 , C12N15/62 , C12N15/11 , C12N9/22 , C12N15/86 , C07K14/47
摘要: Objects to be achieved are to provide a nerve cell with which it is possible to visualize and quantify the intracellular tau without using the exogenous promoter and to provide a pluripotent stem cell with which the nerve cell can be produced, to provide a method of screening a substance, including using the pluripotent stem cell or nerve cell described above, and a substance screened by the above method, and to provide a kit including a targeting vector and a gRNA.
There is provided a pluripotent stem cell including a DNA encoding a reporter molecule, the DNA being introduced adjacent to an endogenous tau gene such that a tau protein is expressed as a fusion protein fused with a reporter molecule.-
公开(公告)号:US20200299643A1
公开(公告)日:2020-09-24
申请号:US16086206
申请日:2017-03-27
申请人: KEIO UNIVERSITY
发明人: Hideyuki OKANO , Wado AKAMATSU , Koki FUJIMORI , Takuya MATSUMOTO , Naoko KUZUMAKI , Fumihiko KISA
IPC分类号: C12N5/0797 , C12N5/10
摘要: A culture medium for inducing a pluripotent stem cell into a differentiation-promoted pluripotent stem cell, the medium including a Glycogen synthase kinase 3β (GSK3β) inhibitor, a Bone morphogenic protein (BMP) signaling inhibitor, and a Transforming growth factor (TGF)-β inhibitor as active ingredients.
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公开(公告)号:US20170340586A1
公开(公告)日:2017-11-30
申请号:US15544419
申请日:2016-01-13
申请人: Keio University
发明人: Makoto HOSOYA , Masato FUJIOKA , Hideyuki OKANO , Kaoru OGAWA , Tatsuo MATSUNAGA
IPC分类号: A61K31/155 , G01N33/50 , A61K31/439
CPC分类号: A61K31/436 , A61K31/155 , A61K31/439 , A61P27/16 , G01N33/5044 , G01N2510/00
摘要: An object of the present invention is to provide novel apoptosis inhibitors and therapeutic agents for inner ear hearing impairment. As a pharmaceutical agent for this purpose, biguanide compounds represented by the following structural formula (I) or a rapamycin derivative represented by the following structural formula (II) as an active ingredient is provided: wherein R1 to R7 are each independently selected from a hydrogen atom, a halogen atom, or a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, a 5- or 6-membered heteroaryl group, or a 5- or 6-membered non-aromatic heterocyclic group, each of which may have a substituent selected from a halogen atom, a cyano group, a C1-6 alkyl group, a C1-6 alkoxy group, a C1-6 alkoxy carbonyl group, a C3-8 cycloalkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, and a phenyl group; wherein R1 is a C1-6 alkyl or a C3-6 alkynyl, R2 is H, —CH2-OH or —CH2—CH2OH, and X is ═O, (H, H) or (H, OH).
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公开(公告)号:US20220380725A1
公开(公告)日:2022-12-01
申请号:US17773784
申请日:2020-11-05
申请人: JSR Corporation , KEIO UNIVERSITY
摘要: According to a production method for a brain organoid, comprising a step 1 of carrying out suspension culture of human pluripotent stem cells having a mutation in at least one or more base sequences in an exon selected from the group consisting of an exon 9, an exon 10, an exon 11, an exon 12, and an exon 13 of a microtubule-associated protein tau (MAPT) gene, and having a mutation in at least one or more base sequences in an intron 10 of the MAPT gene, it is possible to produce a brain organoid having a phosphorylated 3-repeat tau protein and a phosphorylated 4-repeat tau protein.
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公开(公告)号:US20220127567A1
公开(公告)日:2022-04-28
申请号:US17275395
申请日:2019-09-09
申请人: KEIO UNIVERSITY
发明人: Satoru MORIMOTO , Zhi ZHOU , Hideyuki OKANO
摘要: A method for producing astrocytes includes a step of dissociating an embryoid body into single cells and suspension-culturing the cells in a serum-free medium containing basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF) to obtain a neural stem cell mass, and a step of dissociating the neural stem cell mass into single cells and adhesion-culturing the cells in a serum-free medium to obtain a cell population containing astrocytes.
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