IP Library Granted Patent US 9,932,556
Granted Patent B2
US 9,932,556 · App. 14/515,884 · Granted Apr 3, 2018

Method for in vitro differentiation of blood circulating cells into neuronal-like cells and applications thereof

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Quick Facts
Patent No.
US 9,932,556
App. No.
14/515,884
Granted
Apr 3, 2018
Kind
B2
Abstract

The present invention relates to a method for in vitro differentiation of a population of blood circulating cells, such as monocytes and preferably pluripotent macrophages derived therefrom, into cells displaying functional and phenotypic neuronal characteristics. The invention further encompasses neuronal-like cells obtainable according to the present method, compositions comprising said cells, and applications thereof.

Claims (20)

1. A method for in vitro differentiation of a population of pluripotent macrophages into a population of functional neuronal-like cells, wherein:

1) a population of pluripotent macrophages is grown in a culture medium; and

2) exogenous factors BHA (Butylated hydroxyanisole), RA (Retinoic Acid), IGF-1 (Insulin growth factor-1), and NT-3 (Neurotrophin) are added to the culture medium of step 1),

wherein said pluripotent macrophages express the CD11B and CD14 surface antigen markers.

2. The method according to claim 1 , comprising the prior step of differentiating a population of monocytes into a population of pluripotent macrophages.

3. The method according to claim 1 , comprising the prior step of differentiating a population of monocytes into a population of pluripotent macrophages,

wherein the differentiation of said population of monocytes into said population of pluripotent macrophages is obtained by:

a) growing a population of monocytes in a culture medium; and

b) adding the exogenous factor M-CSF (Macrophage colony-stimulating factor) to the medium of step a).

4. The method according to claim 1 , wherein the exogenous factors of step 2) are sequentially added to the culture medium of step 1), in the following order:

i) BHA (Butylated hydroxyanisole);

ii) RA (Retinoic acid); and

iii) IGF-1 (Insulin growth factor-1) and NT-3 (Neurotrophin-3).

5. The method according to claim 4 , further comprising the step of: iv) adding at least one agent capable of stimulating calcium influx to the medium of step iii).

6. The method according to claim 4 , wherein the BHA (Butylated hydroxyanisole) final concentration in step i) is comprised between about 50 nM and about 200 nM.

7. The method according to claim 4 , wherein the RA (Retinoic Acid) final concentration in step ii) is comprised between about 10 μM and about 20 μM.

8. The method according to claim 4 , wherein:

the IGF-1 (Insulin growth factor-1) final concentration in step iii) is comprised between about 5 ng/ml and about 250 ng/ml; and

the NT-3 (Neurotrophin-3) final concentration in step iii) is of up to about 30 ng/ml.

9. The method according to claim 4 , wherein said BHA (Butylated hydroxyanisole) final concentration is adjusted before step iii) to a concentration comprised between about 50 μM and about 100 μM.

Assignments (3)
CHANGE OF NAME Recorded May 12, 2022
From: UNIVERSITE DE PARIS
To: UNIVERSITÉ PARIS CITÉ
Reel/Frame 059988/0388 →
MERGER Recorded May 12, 2022
From: UNIVERSITE PARIS DESCARTES
To: UNIVERSITE DE PARIS
Reel/Frame 060044/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2015
From: HOSMALIN, ANNE; FEUILLET, VINCENT; KREBS, MARIE-ODILE; JAY, THERESE; BELLON, ALFREDO
To: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS); UNIVERSITE PARIS DESCARTES; INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM); ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS
Reel/Frame 034965/0825 →