Method for inducing dopaminergic neuron progenitor cells

US11473058B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11473058-B2
Application numberUS-201414916696-A
CountryUS
Kind codeB2
Filing dateSep 4, 2014
Priority dateSep 5, 2013
Publication dateOct 18, 2022
Grant dateOct 18, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides a method for producing dopaminergic neuron progenitor cells from pluripotent stem cells, which method comprises the steps of: (i) performing adherent culture of pluripotent stem cells on an extracellular matrix in a medium containing a reagent(s) selected from the group consisting of BMP inhibitor, TGFβ inhibitor, SHH signal-stimulating agent, FGF8, and GSK3β inhibitor; (ii) collecting Corin- and/or Lrtm1-positive cells from the cells obtained in Step (i) using a substance which binds to Corin and/or a substance which binds to Lrtm1; and (iii) performing suspension culture of the cells obtained in Step (ii) in a medium containing a neurotrophic factor.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for producing dopaminergic neuron progenitor cells from pluripotent stem cells, said method comprising the steps of: (a) culturing pluripotent stem cells on an extracellular matrix in a medium containing a BMP inhibitor and a TGFβ inhibitor for at least one day, wherein said extracellular matrix is laminin or a fragment(s) thereof; (b) replacing the medium from Step (a) with a medium containing a BMP inhibitor, a TGFβ inhibitor, a SHH signal-stimulating agent, and FGF8 and further culturing the cells for at least one day; (c) replacing the medium from Step (b) with a medium containing a BMP inhibitor, a TGFβ inhibitor, a SHH signal-stimulating agent, FGF8, and a GSK3β inhibitor and further culturing the cells for at least one day; (d) replacing the medium from Step (c) with a medium containing a BMP inhibitor and a GSK3β inhibitor and further culturing the cells for at least one day; and (e) suspending the cells obtained in Step (d); (f) collecting Corin- and/or leucine-rich repeats and transmembrane domains 1 (Lrtm1) positive cells from the cells obtained in Step (e) using an antibody that binds to Corin and/or an antibody that binds to Lrtm1; and (g) culturing the cells obtained in Step (f) in suspension in a medium containing a neurotrophic factor, wherein Step (g) is carried out for at least 7 days, and wherein Steps (a)-(e) are performed within 10 to 21 days. 2. The method according to claim 1 , wherein said neurotrophic factor is BDNF and GDNF. 3. The method according to claim 1 , wherein the medium in Step (g) further comprises B27 supplement, ascorbic acid, and dibutyryl cyclic AMP. 4. The method according to claim 1 , wherein said Steps (a-e) is carried out for 12 days to 21 days. 5. The method according to claim 1 , wherein said Step (g) is carried out for 14 days to 30 days. 6. The method according to claim 1 , wherein said extracellular matrix is laminin 511E8. 7. The method according to claim 1 , wherein said BMP inhibitor is selected from the group consisting of Chordin, Noggin, Follistatin, Dorsomorphin and LDN193189, wherein said TGFβ inhibitor is selected from the group consisting of Lefty-1, SB431542, SB202190, SB505124, NPC30345, SD093, SD908, SD208, LY2109761, LY364947, LY580276 and A83-01, wherein said SHH signal-stimulating agent is selected from the group consisting of SHH, Hh-Ag1.5, SAG, 20a-hydroxycholesterol and purmorphamine, and wherein said GSK3β inhibitor is selected from the group consisting of BIO, 6-bromoindirubin-3′-oxime, SB216763, GSK-3β inhibitor VII, L803-mts and CHIR99021. 8. The method according to claim 1 , wherein said BMP inhibitor is LDN193189, wherein said TGFβ inhibitor is A83-01, wherein said SHH signal-stimulating agent is purmorphamine, and wherein said GSK3β inhibitor is CHIR99021.

Assignees

Inventors

Classifications

  • from embryonic cells · CPC title

  • Neurons · CPC title

  • Transforming growth factor beta (TGF-β) · CPC title

  • A61K35/30Primary

    Nerves; Brain; Eyes; Corneal cells; Cerebrospinal fluid; Neuronal stem cells; Neuronal precursor cells; Glial cells; Oligodendrocytes; Schwann cells; Astroglia; Astrocytes; Choroid plexus; Spinal cord tissue · CPC title

  • from non-embryonic pluripotent stem cells · CPC title

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What does patent US11473058B2 cover?
The present invention provides a method for producing dopaminergic neuron progenitor cells from pluripotent stem cells, which method comprises the steps of: (i) performing adherent culture of pluripotent stem cells on an extracellular matrix in a medium containing a reagent(s) selected from the group consisting of BMP inhibitor, TGFβ inhibitor, SHH signal-stimulating agent, FGF8, and GSK3β inhi…
Who is the assignee on this patent?
Univ Kyoto, Univ Osaka, Eisai R&D Man Co Ltd
What technology area does this patent fall under?
Primary CPC classification A61K35/30. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Oct 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).