Trans-Differentiation And Re-Differentiation Of Somatic Cells And Production Of Cells For Cell Therapies

a somatic cell and transdifferentiation technology, applied in the field of somatic cell transdifferentiation and redifferentiation, can solve the problems of unanticipated plasticity in the ability to transdifferentiate stem cells, the inability to complete the conversion to a fully functional and stable and the inability to fully function and stabilize the different type of cell has never been demonstrated

Inactive Publication Date: 2010-05-13
PAGE RAYMOND +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0012]The present invention utilizes a cell's ability to respond to environmental factors after they have been “primed” to do so in vitro. Priming is achieved by destabilizing cell's cytoskeletal structure, consequently removing the feedback mechanisms between cell's shape and nuclear function. Both, shape and function define the specificity of any cell type. The human cell types used as a source are differentiated somatic cells, such as fibroblasts and keratinocytes from skin biopsies, and leukocytes from blood samples. Cell structure is first destabilized with cytoskeletal inhibitors, consequently their nuclear structure becomes permissive to alteration and upon exposure to conditions that promote or support a desired cell type such that the primed cells acquire this new morphology and function. Primed cells are multipotent and, upon application of factors that induce formation of the central nervous system are capable of differentiating into different neurons, astrocytes, or oligodendrocytes. The result is populations of newly differentiated neuronal cell types genetically identical to the fibroblasts sampled from the donor. The present invention overcomes barriers and limitations to the derivation of patient-specific cells, which are: the need for embryos as a source of embryonic stem cells, histo-incompatibility between the donor and the recipient, the risk of transmitting animal viruses via xenotransplantation, insufficient quantities of cells / tissues for transplantation, and high cost associated with generation of embryos and embryonic stem cells, life-long immunosuppression, and the requirement for repeated treatments.

Problems solved by technology

In addition, some types of stem cells are displaying an unanticipated plasticity in their ability to trans-differentiate into other types of cells when transplanted from their niche into heterologous tissue compartments.
Despite these developments, problems of stem cell accessibility and quantity persist.
However, complete conversion to a fully functional and stable different type of cell has never been demonstrated.

Method used

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  • Trans-Differentiation And Re-Differentiation Of Somatic Cells And Production Of Cells For Cell Therapies
  • Trans-Differentiation And Re-Differentiation Of Somatic Cells And Production Of Cells For Cell Therapies
  • Trans-Differentiation And Re-Differentiation Of Somatic Cells And Production Of Cells For Cell Therapies

Examples

Experimental program
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Effect test

example 1

[0070]Bovine fetal fibroblasts (BFFs) were grown to confluence and seeded onto 100 mm plates at approximately 250,000 cells / plate. Cells were grown in DMEM (Gibco) supplemented with 0.03% L-Glutamine (Sigma), 100 μM non-essential amino acids (Gibco), 10 units / L Penicillin-Streptomycin (Gibco), 154 μM 2-Mercaptoethanol (Gibco) and 15% FBS (HyClone). Four treatments were used:[0071]1. A control grown in the medium described above,[0072]2. DMEM with 2.5 μg / ml CB,[0073]3. DMEM with 5.0 μg / ml CB, and[0074]4. DMEM with 7.5 μg / ml CB.

[0075]Control cells were grown in the presence of DMSO alone to evaluate its effect on priming and trans-differentiation.

[0076]BFFs cultured in treatment 1 began to rapidly divide and grow to confluence as was expected. BFFs cultured in treatment 2 did not undergo cytokinesis, however did undergo nuclear division leading to multinuclear fibroblasts. BFFs cultured in treatments 3 and 4 began to change morphology and by day 2 of treatment began to take on the app...

example 2

[0078]Bovine adult fibroblasts (BAFs) were treated in the manner described for BFFs in Example 1, with priming carried out using 10.0 μg / ml CB for 72 hours. Like BFFs, treatment of the BAFs with the priming agent and culturing them under conditions that induce neural differentiation caused the cells to undergo morphological changes toward a neuronal-like lineage. See FIGS. 3 and 4. Note that BFFs and BAFs acquire different morphologies of a neural type.

example 3

[0079]Transdifferentiation of human neo-natal fibroblasts. Fibroblasts were purchased from Cambrex company (Clonetics cell line # CC-2509) and were expanded in Iscove's Modified Dulbecco's Medium (IMDM, Gibco) supplemented with 20% fetal bovine serum (HyClone) at 37° C. in 5% CO2 and 5% O2. At passage 14, cells were weaned from serum by replacing medium every other day with half the concentration of serum over a 2-week period. When cells had been in the absence of serum for 48 hours, they were seeded at 50% confluency in 24-well dishes. 24 hours after passage, IMDM was removed and replaced with conducive medium (keratinocyte growth medium (KGM, Clonetics) was added to half of the cultures and neuro-progenitor growth medium (NPMM, Clonetics) was added to the other half). After 24 hours in conducive medium, 5 ug / ml cytochalasin B (CB, CalBiochem) was supplemented into half of each media group. Cells were cultured for an additional 72 hours at which point half of all groups were fixed ...

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Abstract

The invention provides a method for effecting the trans-differentiation of a somatic cell, i.e., the conversion of a somatic cell of one cell type into a somatic cell of a different cell type. The method is practiced by culturing a somatic cell in the presence of at least one agent selected from the group consisting of (a) cytoskeletal inhibitors and (b) inhibitors of acetylation, and (c) inhibitors of methylation, and also culturing the cell in the presence of agents or conditions that induce differentiation to a different cell type. The method is useful for producing histocompatible cells for cell therapy.

Description

RELATED APPLICATIONS[0001]This application is a continuation of U.S. Ser. No. 10 / 228,296 filed Aug. 27, 2002, which claims benefit of priority to U.S. Ser. No. 60 / 314,654 filed on Aug. 27, 2001, each of which is incorporated by reference in its entirety herein.FIELD OF THE INVENTION[0002]This application relates to methods for effecting trans-differentiation of somatic cells. Trans-differentiation is the conversion of a cell from one differentiated cell type to another differentiated cell type.BACKGROUND OF THE INVENTION[0003]Stem cells obtained from adults (mesenchymal, hematopoietic, neuronal) are receiving increasing interest as a source of material for cell and tissue transplantation to treat human disease. To a large degree, this interest has been stimulated by findings that report the presence of certain types of stem cells in unexpected tissue compartments in vivo (e.g. neuronal stem cells in bone marrow). In addition, some types of stem cells are displaying an unanticipated ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N5/071C12N5/00C12Q1/02A61K35/12C12N5/02C12N5/079
CPCA61K35/12C12N5/0618C12N2506/1307C12N2501/999C12N2501/70
Inventor PAGE, RAYMONDDOMINKO, TANJAMALCUIT, CHRISTOPHER
Owner PAGE RAYMOND
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