Neuronal cell cultures as compute substrates
US-2024386258-A1 · Nov 21, 2024 · US
US9896656B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9896656-B2 |
| Application number | US-201414216391-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 17, 2014 |
| Priority date | Mar 15, 2013 |
| Publication date | Feb 20, 2018 |
| Grant date | Feb 20, 2018 |
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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.
Opening claim text (preview).
The invention claimed is: 1. A transplantable innervated smooth muscle construct, comprising: a biocompatible hydrogel substrate comprising at least one of collagen, laminin and heparan sulfate; a population of longitudinal smooth muscle cells of enteric origin formed as a muscle cell sheet on a mold containing a wavy microtopography and disposed in contact with the hydrogel substrate; and a population of neural stem cells initially seeded in the hydrogel and induced to differentiate and innervate the muscle cell sheet. 2. The construct of claim 1 wherein the smooth muscle cell sheet further comprises axially-aligned longitudinal smooth muscle cells. 3. The construct of claim 1 wherein the hydrogel comprises collagen. 4. The construct of claim 1 wherein the hydrogel comprises at least 800 μg/ml of collagen type I. 5. The construct of claim 1 wherein the hydrogel further comprises at least 200 μg/ml of collagen type IV. 6. The construct of claim 1 wherein the hydrogel further comprises at least 5 μg/ml of laminin. 7. The construct of claim 1 wherein the hydrogel is substantially free of laminin. 8. The construct of claim 1 wherein the hydrogel is substantially free of heparan sulfate. 9. The construct of claim 1 wherein the hydrogel comprises a hydrogel sponge with effective pore sizes ranging from 10 nanometers to 10 micrometers. 10. The construct of claim 1 wherein the neural stem cells are differentiated into at least one neuronal subtype. 11. The construct of claim 10 wherein the substrate comprises collagen I and the at least one neuronal subtype comprises cholinergic neurons. 12. The construct of claim 10 wherein the substrate comprises collagen I and collagen IV and the at least one neuronal subtype comprises nitrergic neurons. 13. The construct of claim 10 wherein the substrate comprises laminin and heparan sulfate and the at least one neuronal subtype comprises peptidergic neurons. 14. The construct of claim 10 wherein the substrate is substantially free of laminin and heparan sulfate and the at least one neuronal subtype comprises glial cells.
Collagen; Gelatin · CPC title
Fibronectin; Laminin · CPC title
Glial cells, e.g. astrocytes, oligodendrocytes; Schwann cells · CPC title
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
Substrates of biological origin, e.g. extracellular matrix, decellularised tissue · CPC title
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