Avian induced pluripotent stem cells and their use

a technology of stem cells and avian genus, which is applied in the direction of genetically modified cells, skeletal/connective tissue cells, antibody medical ingredients, etc., can solve the problems of not being able to produce non-mammal ipscs, not being able to meet the needs of mammalian species, and not being able to efficiently undergo directed in vitro differentiation. , to achieve the effect of accelerating recovery rate, reducing the number of cells, and improving survival

Inactive Publication Date: 2014-12-11
UNIV OF GEORGIA RES FOUND INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0045]In a further embodiment, a method referred to as the aiPSC/aiPGC virus exposure survival and recovery assay is used to determine the resistance of cells in a sample. In this assay a sample of resistant aiPSCs or resistant aiPGCs which have been exposed previously to a disease agent (e.g. ND virus) is plated, exposed to the disease agent and then measured to determine viability. Resistant cells evidence higher cell numbers at earlier points in time and a more rapid increase in cell numbers over time at la

Problems solved by technology

Additionally, many of these avian lines have not been shown to robustly undergo directed in vitro differentiation into multiple lineages with phenotypic characteristic similar to mammalian pluripotent cells.
Generating non-mammal iPSCs faces other challenges and difficulties.
This is not possible in mammalian species.
Correct development of these cells is essential and perturbation in their development often leads to reproductive failure and disease.

Method used

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  • Avian induced pluripotent stem cells and their use
  • Avian induced pluripotent stem cells and their use
  • Avian induced pluripotent stem cells and their use

Examples

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EXAMPLES / RESULTS

Quail Pluripotent Stem Cells

[0285]qiPSCs Display Morphological Characteristics Consistent with a Pluripotent Cell Type

[0286]The generation of qiPSCs was initiated by testing the lentiviral transduction efficiency of isolated (QEF) (FIG. 1A) with an eGFP reporter construct using both GeneJammer and TransDux transduction reagents. A 20 MOI transduction with Transdux resulted in the highest efficiency with 40.5% (GFP) positive cells (S. FIG. 1). QEFs were then transduced with the six human pluripotency genes hPOU5F1, hNANOG, hSOX2, hLIN28, hC-MYC and hKLF4 driven by the elongation factor 1-alpha (EF1-α) promoter with each construct in individual lentiviral vectors. After 24 hrs, cells were replated on feeder cells in stem cell expansion medium.

[0287]Colonies were observed beginning 6 days after transduction with irregular shaped borders and fibroblast-like cell morphology (FIG. 1B). These initial colonies failed to proliferate and expand indicating that these colonies w...

example

Chicken Induced Pluripotent Stem Cells Using a Non Integrating System

[0342]The benefits of non integrating systems are the following: The molecular basis of reprogramming has been revealed by exogenous expression of combinations of transcription factors described in prior examples for quail and chicken, described above. Induction of reprogramming was carried by these factors is mostly carried out by co-infection with retroviral or lentiviral vectors. The main problems of the retrovirus-based method are oncogenicity and mutagenesis. Chimeric mice derived from iPSCs as well as their offspring developed tumors, probably because of reactivation of the proviral cMyc oncogene. Even though three-factor (Oct4, Sox2, and Klf4) iPSC-derived animals did not develop tumors, ectopic expression of any one of these genes may have deleterious consequences. For instance, ectopic expression of Oct4 in skin and intestine causes tumor development. Overexpression of Klf4 induces dysplasia in skin.

[0343]...

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Abstract

The present invention relates to the production of avian induced pluripotent stem cells from non-pluripotent somatic cells, including embryonic fibroblasts and adult somatic cells. In this method, avian (including quail or chicken) somatic cells are reprogrammed into a state closely resembling embryonic stem cells including the expression of key stem cell markers alkaline phosphatase, etc. by transfecting/transducing the non-stem cells with genes (preferably using a non-integrating vector as otherwise described herein or alternatively an integrating vector, such a lentiviral vector, retroviral vector or inducible lentiviral vector, among others) which express at least nanog, Lin28 and cMyc. In preferred aspects of the invention, the transfected/transduced vectors express nanog, Lin28, cMyc, Oct 4 (POU5F1 or PouV), SOX2 and KLF4. The induced stem cells which are produced contribute to all 3 germ layers, the trophectoderm and in certain aspects, the gonad in chimeric offspring.

Description

RELATED APPLICATIONS AND GRANT SUPPORT[0001]This application is a continuation-in-part application claiming the benefit of priority of international application PCT / US2012 / 041873, filed 11 Jun., 2012, entitled “Avian Induced Pluripotent Stem Cells and Their Use”, which claims the benefit of priority of provisional application Ser. No. 61 / 495,499, filed Jun. 10, 2011 entitled “Avian Induced Pluripotent Stem Cells Generate Live Quail-chicken Chimeras and Undergo Advanced In Vitro Differentiation” the contents of each of said applications being incorporated by reference in their entirety herein.FIELD OF THE INVENTION[0002]The present invention relates to the production of avian induced pluripotent stem cells from non-pluripotent somatic cells, including embryonic fibroblasts and adult somatic cells. In this method, avian (including quail or chicken) somatic cells are reprogrammed into a state closely resembling embryonic stem cells including the expression of key stem cell markers alka...

Claims

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Application Information

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IPC IPC(8): A01K67/027
CPCA01K67/0275C12N2501/60C12N2501/602C12N2501/605C12N2501/608C12N2502/99C12N2506/1307A01K67/0271A01K2207/12A01K2227/30A01K2267/02C12N2760/16111C12N2760/18111C12N2999/007C12N5/0696C12N2501/603C12N2506/02
Inventor STICE, STEVEN L.WEST, FRANKLINLU, YANGQING
Owner UNIV OF GEORGIA RES FOUND INC
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