Neural progenitor cell differentiation

Patent metadata

Field	Value
Publication number	US-10377985-B2
Application number	US-201815875717-A
Country	US
Kind code	B2
Filing date	Jan 19, 2018
Priority date	Mar 15, 2013
Publication date	Aug 13, 2019
Grant date	Aug 13, 2019

Abstract

Differentiation and stability of neural stem cells can be enhanced by in vitro or in vivo culturing with one or more extracellular matrix (ECM) compositions, such as collagen I, IV, laminin and/or a heparan sulfate proteoglycan. In one aspect of the invention, adult mammalian enteric neuronal progenitor cells can be induced to differentiate on various substrates derived from components or combinations of neural ECM compositions. Collagen I and IV supported neuronal differentiation and extensive glial differentiation individually and in combination. Addition of laminin or heparan sulfate to collagen substrates unexpectedly improved neuronal differentiation, increasing neuron number, branching of neuronal processes, and initiation of neuronal network formation. In another aspect, neuronal subtype differentiation was affected by varying ECM compositions in hydrogels overlaid on intestinal smooth muscle sheets. The matrix compositions of the present invention can be used to tissue engineer transplantable innervated GI smooth muscle constructs to remedy aganglionic disorders.

First claim

The invention claimed is:

1. A method of preparing an innervated smooth muscle construct, the method comprising:
obtaining a population of longitudinal smooth muscle cells;
culturing the longitudinal smooth muscle cells to form a uniaxially-aligned smooth muscle sheet;
obtaining a population of neural stem cells
and
co-culturing the neural stem cells and the uniaxially-aligned smooth muscle sheet on a hydrogel substrate comprising at least one of collagen, laminin and heparan sulfate.

2. The method of claim 1 wherein the step of culturing the longitudinal smooth muscle cells further comprises culturing the muscle cells on a mold containing a wavy microtopography to form the uniaxially-aligned smooth muscle sheet.

3. The method of claim 1 wherein the hydrogel comprises collagen.

4. The method of claim 1 wherein the hydrogel comprises at least 800 μg/ml of collagen type I.

5. The method of claim 4 , wherein the hydrogel comprises between about 800 μg/ml and about 1600 μg/ml collagen I.

6. The method of claim 1 wherein the hydrogel further comprises at least 200 μg/ml of collagen type IV.

7. The method of claim 1 wherein the hydrogel further comprises at least 5 μg/ml of laminin.

8. The method of claim 1 wherein the hydrogel is substantially free of laminin.

9. The method of claim 1 wherein the hydrogel is substantially free of heparan sulfate.

10. The method of claim 1 wherein the method further comprises administering the construct to a patient.

11. The method of claim 10 , wherein the step of administering the construct further comprises implanting the construct into the patient.

12. The method of claim 11 wherein the construct comprises a hydrogel sponge with effective pore sizes ranging from 10 nanometers to 10 micrometers.

Assignees

• Univ Wake Forest Health Sciences

Inventors

• Bitar Khalil

Classifications

• C12N5/0622

  Glial cells, e.g. astrocytes, oligodendrocytes; Schwann cells · CPC title

• C12N2533/52

  Fibronectin; Laminin · CPC title

• C12N2533/90

  Substrates of biological origin, e.g. extracellular matrix, decellularised tissue · CPC title

• A61K35/34

  Muscles; Smooth muscle cells; Heart; Cardiac stem cells; Myoblasts; Myocytes; Cardiomyocytes (vascular smooth muscle A61K35/44) · CPC title

• C12N5/0619 Primary

  Neurons · CPC title