Methods and compositions for promoting survival and proliferation of endothelial cells and stimulating angiogenesis
The present invention relates to adenovirus E4ORF1 gene and to endothelial cells engineered to express the E4ORF1 gene. The present invention also relates to uses of the E4ORF1 gene, and cells expressing the E4ORF1 gene, and to compositions comprising the E4ORF1 gene, or comprising cells expressing the E4ORF1 gene.
1. A composition comprising a population endothelial cells, wherein the endothelial cells
(a) comprise a recombinant nucleic acid sequence that comprises an E4ORF1 coding sequence under the control of a promoter, and
(b) do not comprise nucleic acid sequences that comprise the entire adenovirus E4 region.
2. The composition of claim 1 , wherein the recombinant nucleic acid sequence is comprised within a lentiviral vector.
3. The composition of claim 1 , wherein the recombinant nucleic acid sequence is comprised within an adenoviral vector.
4. The composition of claim 1 , wherein the recombinant nucleic acid sequence further comprises an antibiotic resistance gene.
5. The composition of claim 1 , wherein the recombinant nucleic acid sequence further comprises a reporter gene or a sequence encoding an expression tag.
6. The composition of claim 5 , wherein the recombinant nucleic acid sequence encodes green fluorescent protein (GFP).
7. The composition of claim 1 , wherein the promoter is selected from the group consisting of a CMV promoter, an SV40 promoter, an RSV promoter, an HIV-Ltr promoter, and an MML promoter.
8. The composition of claim 1 , wherein the promoter is an adenovirus promoter.
9. The composition of claim 1 , wherein the promoter is an inducible promoter.
10. The composition of claim 1 , wherein the E4ORF1 coding sequence is a human adenovirus type 5 coding sequence.
11. The composition of claim 1 , wherein the E4ORF1 coding sequence comprises SEQ ID NO. 1.
12. The composition of claim 1 , wherein the E4ORF1 coding sequence is an E4ORF1 coding sequence from human adenovirus 1, human adenovirus 2, human adenovirus 3, human adenovirus 7, human adenovirus 9, human adenovirus 11, human adenovirus 12, human adenovirus 14, human adenovirus 34, human adenovirus 35, human adenovirus 46, human adenovirus 50, or human adenovirus 52.
13. The composition of claim 1 , where the endothelial cells are selected from the group consisting of: testis endothelial cells, lung endothelial cells, lymphatic endothelial cells, cord blood endothelial cells, umbilical vein endothelial cells, heart endothelial cells, skin endothelial cells, liver endothelial cells, brain endothelial cells, bone endothelial cells, and pancreatic endothelial cells.
14. The composition of claim 1 , further comprising a population of cancer cells, stem cells, or progenitor cells.
15. The composition of claim 14 , wherein the stem cells or progenitor cells are selected from the group consisting of embryonic stem cells, hematopoietic stem or progenitor cells, neural stem or progenitor cells, skin stem or progenitor cells, spermatogonial stem or progenitor cells, and gut stem or progenitor cells.
16. The composition of claim 1 , further comprising a population of hematopoietic stem or progenitor cells.
17. The composition of claim 1 , further comprising Matrigel.
18. The composition of claim 1 , further comprising a physiological saline solution or a carrier solution suitable for administration to a living subject.
19. A method of inducing angiogenesis in vivo, the method comprising administering a composition according to claim 1 to a subject in need thereof.
20. A method of inducing wound healing in vivo, the method comprising administering a composition according to claim 1 to a subject in need thereof.
21. A method for maintaining or expanding cancer cells, stem cells or progenitor cells in vitro, the method comprising:
a. contacting cancer cells, stem cells or progenitor cells in vitro with conditioned medium, wherein the condition medium is derived from a culture of E4ORF1-expressing endothelial cells that do not contain or express nucleic acid sequences that comprise the entire adenovirus E4 region,
thereby maintaining or expanding the cancer cells, stem cells or progenitor cells in vitro.
22. A method of maintaining or expanding cancer cells, stem cells or progenitor cells in vitro, the method comprising:
b. culturing a population of cancer cells, stem cells or progenitor cells in vitro in a culture vessel that comprises a population of E4ORF1-expressing endothelial cells, wherein the endothelial cells do not contain or express nucleic acid sequences that comprise the entire adenovirus E4 region,
thereby maintaining or expanding the cancer cells, stem cells or progenitor cells in vitro.