Andrezej Ptasznik - Philadelphia PA Alberti Hayek - La Jolla CA Gillian M. Beattie - Poway CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12N 506
US Classification:
435377, 375366
Abstract:
This invention pertains to the discovery that inhibition of phosphatidylinositol 3-kinase (PI3K) in human fetal undifferentiated cells induces morphological and functional endocrine differentiation. This is associated with an increase in mRNA levels of insulin, glucagon, and somatostatin, as well as an increase in the insulin protein content and secretion response to secretagogues. Blockade of PI3K also increases the proportion of pluripotent precursor cells coexpressing multiple hormones and the total number of terminally differentiated cells originating from these precursor cells.
Development And Use Of Human Pancreatic Cell Lines
Fred Levine - Del Mar CA, US Sijian Wang - Dallas TX, US Gillian Beattie - Poway CA, US Alberto Hayek - La Jolla CA, US
International Classification:
A61K048/00 C12N015/867 C12N005/08
US Classification:
424/093210, 435/456000, 435/366000, 435/320100
Abstract:
This invention relates to cell lines, particularly mammalian cell lines, established by transforming the cells with vectors, preferably retroviral vectors, containing two or more oncogenes under the control of one or more inducible promoters and/or genetic elements. Also within the scope of the invention are human cell lines with extended in vitro lifespan, transformed by vectors containing one or more oncogenes under the control of one or more, preferably exogenous, inducible promoters and/or genetic elements. The vectors may additionally contain gene(s) encoding for desired gene product(s). Also disclosed are insulin producing human pancreatic cell lines useful for transplantation into human diabetic patients.
Gillian Beattie - San Diego CA, US Alberto Hayek - La Jolla CA, US Anthony Montgomery - Cardiff CA, US
Assignee:
Regents of the University of California
International Classification:
A61K045/00 C12N005/08
US Classification:
424/093700, 435/366000
Abstract:
The present invention provides a method of culturing cells on a matrix. The present invention includes islet cells cultured in a 3-D configuration in the presence of a fibrin matrix support. Induction of -cell proliferation with HGF/SF is also provided.
Compositions And Methods For Growth Of Embryonic Stem Cells
Alberto Hayek - La Jolla CA, US Gillian Beattie - San Diego CA, US Ana Lopez - San Diego CA, US
International Classification:
A61K 45/00 C12N 5/08 A61P 35/00
US Classification:
424 937, 435374, 435366
Abstract:
The present invention relates to methods, compositions, and kits for maintenance of the undifferentiated state and/or pluripotency in stem cells, including embryonic stem (ES) cells. It also relates to stem cells that have been maintained in an undifferentiated state. The present invention provides these aspects using culture medium enriched with a TGFβ family member protein, an FGF family member protein, and/or nicotinamide, without using fibroblast feeder layers, conditioned media, or leukemia inhibitory factor.
Method Of Stimulating Proliferation And Differentiation Of Human Fetal Pancreatic Cells Ex Vivo
Jeffrey Rubin - Rockville MD Alberto Hayek - La Jolla CA Gillian M. Beattie - Poway CA Timo P. J. Otonkoski - La Jolla CA
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC Whittler Institute for Diabetes and Endocrinology - La Jolla CA
International Classification:
C12N 500 C12N 502
US Classification:
4352402
Abstract:
A method of inducing the proliferation and/or differentiation of human fetal pancreatic cells entails contacting such cells in primary culture with Hepatocyte Growth Factor/Scatter Factor, thereby inducing a proliferation of. beta. -epithelial cells, an increase in the number of. beta. -epithelial cells which form islet-like cell clusters, and an increase in insulin production per cell. The method provides increased numbers of functional islet-like cell clusters for transplantation, for example, into Type 1 diabetic patients. The method can be scaled up so as to provide clinically useful numbers of cells for transplantation.
Culturing Human Pancreatic Endocrine Cells In Medium Containing Extracellular Matrix From Human Bladder Carcinoma Cells
Gillian M. Beattie - Poway CA Alberto Hayek - La Jolla CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12N 508 C12N 506 C12N 1100
US Classification:
435366
Abstract:
Human pancreatic endocrine cells are proliferated without loss of hormone function in a culture medium containing extracellular matrix from bladder carcinoma cell lines in the substantial absence of hepatocyte growth factor/scatter factor. Proliferation is preferably carried out in the substantial absence of any peptide growth factors and nicotinamide. The cells may be proliferated in a monolayer on a solid substrate. Islets and islet-like cell clusters are proliferated without loss of insulin-secreting function by incubation in a medium containing extracellular matrix from a human bladder carcinoma cell line, preferably cell line ATCC HTB-9.
Human Pancreatic Cell Lines: Developments And Uses
Fred Levine - Del Mar CA Sijian Wang - San Diego CA Gillian M. Beattie - Poway CA Alberto Hayek - La Jolla CA
Assignee:
Regents of The University of California - Oakland CA
International Classification:
C12N 500 C12N 508 C12N 522 C12N 1563
US Classification:
435325
Abstract:
This invention relates to cell lines, particularly mammalian cell lines, established by transforming the cells with vectors, preferably retroviral vectors, containing two or more oncogenes under the control of one or more inducible promoters and/or genetic elements. Also within the scope of the invention are human cell lines with extended in vitro lifespan, transformed by vectors containing one or more oncogenes under the control of one or more, preferably exogenous, inducible promoters and/or genetic elements. The vectors may additionally contain gene(s) encoding for desired gene product(s). Also disclosed are insulin producing human pancreatic cell lines useful for transplantation into human diabetic patients.
Gillian M. Beattie - Poway CA Douglas A. Lappi - Del Mar CA J. Andrew Baird - San Diego CA Alberto Hayek - La Jolla CA
Assignee:
The Salk Institute for Biological Studies - La Jolla CA The Whittier Institute for Diabetes & Endocrinology - San Diego CA
International Classification:
C12N 506 C12N 508
US Classification:
4352402
Abstract:
The addition of basic FGF-saporin mitotoxins selectively elminates fibroblastoids from human islets in culture and increases the ability of such islets to release insulin under basal and stimulated conditions. When such islets are attached to an extracellular matrix, in particular BCEM, the proliferation of islet cells is favored, and the ability of islets cultured in such manner to release insulin is further increased. Moreover, supplementation of the culture media with high glucose or insulin further improves the functioning of the human islets, resulting in augmented insulin release. Combinations of such procedures offer a novel approach towards the establishment of viable human islet cell monolayers for clinical and laboratory research.
Isbn (Books And Publications)
Women And Marriage in Paul And His Early Interpreters