Plasticity of Human Stem Cells in the Fetal Sheep Model of Human Stem Cell Transplantation

International Journal of Hematology

Volumn 79, Issue 1, 2004, Pages 1-6

  Almeida Porada, Graqa ^a   Porada, Christopher ^a   Zanjani, Esmail D ^a  

^a UNIVERSITY OF NEVADA   (United States)

Author keywords

In utero transplantation; In vivo model; Plasticity; Stem cells; Transdifferentiation

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; CELL DAMAGE; CELL DIFFERENTIATION; CONTROLLED STUDY; EVALUATION; EXPERIMENTAL MODEL; FETUS; FETUS LIVER; GENETIC ANALYSIS; GESTATIONAL AGE; HUMAN; IMMUNE RESPONSE; NONHUMAN; PLASTICITY; REVIEW; SHEEP; STEM CELL TRANSPLANTATION; TISSUE SPECIFICITY;

EID: 0842300402     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02983526     Document Type: Review

References (58)

1. Lagasse E, Connors H, Al-Dhalimy M, et al. Purified hematopoietic stem cells can differentiate into hepatocytes in vivo. Nat Med. 2000;6:1229-1234.
2. Petersen BE, Bowen WC, Patrene KD, et al. Bone marrow as a potential source of hepatic oval cells. Science. 1999;284:1168-1170.
3. Theise ND, Badve S, Saxena R, et al. Derivation of hepatocytes from bone marrow cells of mice after radiation-induced myeloablation. Hepatology. 2000;31:235-240.
4. Krause DS, Theise ND, Collector MI, et al. Multi-organ, multi-lineage engraftment by a single bone marrow-derived stem cell. Cell. 2001;105:369-377.
5. Wagers AJ, Sherwood RI, Christensen JL, Weissman IL. Little evidence for developmental plasticity of adult hematopoietic stem cells. Science. 2002;297:2256-2259.
6. Wang X, Montini E, Al-Dhalimy M, Lagasse E, Finegold M, Grompe M. Kinetics of liver repopulation after bone marrow transplantation. Am J Pathol. 2002;161:565-574.
7. Mallet VO, Mitchell C, Mezey E, et al. Bone marrow transplantation in mice leads to a minor population of hepatocytes that can be selectively amplified in vivo. Hepatology. 2002;35:799-804.
8. Wang X, Ge S, McNamara G, Hao QL, Crooks GM, Nolta JA. Albumin-expressing hepatocyte-like cells develop in the livers of immune-deficient mice that received transplants of highly purified human hematopoietic stem cells. Blood. 2003;101:4201-4208.
9. Theise ND, Nimmakayalu M, Gardner R, et al. Liver from bone marrow in humans. Hepatology. 2000;32:11-16.
10. Alison MR, Poulsom R, Jeffery R, et al. Hepatocytes from nonhepatic adult stem cells. Nature. 2000;406:257.
11. Korbling M, Katz RL, Khanna A, et al. Hepatocytes and epithelial cells of donor origin in recipients of peripheral-blood stem cells. N Engl J Med. 2002;346:738-746.
12. Danet GH, Luongo JL, Butler G, et al. C1qRp defines a new human stem cell population with hematopoietic and hepatic potential. Proc Natl Acad Sci U S A. 2002;99:10441-10445.
13. Schwartz RE, Reyes M, Koodie L, et al. Multipotent adult progenitor cells from bone marrow differentiate into functional hepatocyte-like cells. J Clin Invest. 2002;109:1291-1302.
14. Almeida-Porada G, El Shabrawy D, Porada C, Zanjani ED. Differentiative potential of human metanephric mesenchymal cells. Exp Hematol. 2002;30:1454-1462.
15. Ferrari G, Cusella-De Angelis G, Coletta M, et al. Muscle regeneration by bone marrow-derived myogenic progenitors. Science. 1998;279:1528-1530.
16. Bjornson CRR, Rietze RL, Reynolds BA, et al. Turning brain into blood: a hematopoietic fate adopted by adult neural stem cells in vivo. Science. 1999;283:534-537.
17. Bittner RE, Popoff I, Shorny S, et al. Dystrophin expression in heterozygous mdx/+ mice indicates imprinting of X chromosome inactivation by parent-of-origin-, tissue-, strain- and position-dependent factors. Anat Embryol (Berl). 1997;195:175-182.
18. Gussoni E, Soneoka Y, Strickland CD, et al. Dystrophin expression in the mdx mouse restored by stem cell transplantation. Nature. 1999;401:390-394.
19. Clarke DL, Johansson CB, Wilbertz J, et al. Generalized potential of adult neural stem cells. Science. 2000;288:1660-1663.
20. Watt FM. Epidermal stem cells: markers, patterning and the control of stem cell fate. Philos Trans R Soc Lond B Biol Sci. 1998;353:831-837.
21. Ormerod EJ, Rudland PS. Regeneration of mammary glands in vivo from isolated mammary ducts. J Embryol Exp Morphol. 1986;96:229-243.
22. Seale P, Rudnicki MA. A new look at the origin, function, and "stem-cell" status of muscle satellite cells. Dev Biol. 2000;218:115-124.
23. Gage FH, Ray J, Fisher LJ. Isolation, characterization, and use of stem cells from the CNS. Annu Rev Neurosci. 1995;18:159-192.
24. Eriksson PS, Perfilieva E, Bjork-Eriksson T, et al. Neurogenesis in the adult human hippocampus. Nat Med. 1998;4:1313-1317.
25. Block GD, Locker J, Bowen WC, et al. Population expansion, clonal growth, and specific differentiation patterns in primary cultures of hepatocytes induced by HGF/SF, EGF and TGFα in a chemically defined (HGM) medium. J Cell Biol. 1996;132:1133-1149.
26. Reid GM, Tervit HM. Sudden infant death syndrome: near weightlessness and delayed neural transformation. Med Hypotheses. 1996;46:383-387.
27. Serova LV. The maternal-fetal system as an object for the study of mechanisms of the physiologic effect of weightlessness [in Russian]. Kosm Biol Aviakosm Med. 1987;21:63-66.
28. Wood C. Weightlessness: its implications for the human fetus. J Obstet Gynaecol Br Commonw. 1970;77:333-336.
29. Susse HJ, Wurterle A. The shifting center of gravity in the growing fetus [in German]. Zentralbl Gynakol. 1967;89:980-984.
30. Hammond TG, Benes E, O'Reilly KC, et al. Mechanical culture conditions effect gene expression: gravity-induced changes on the space shuttle. Physiol Genomics. 2000;3:163-173.
31. de Groot RP, Rijken PJ, den Hertog J, et al. Microgravity decreases c-fos induction and serum response element activity. J Cell Sci. 1990;97:33-38.
32. de Groot RP, Rijken PJ, den Hertog J, et al. Nuclear responses to protein kinase C signal transduction are sensitive to gravity. Exp Cell Res. 1991;197:87-90.
33. Walther I, Pippia P, Meloni MA, et al. Simulated microgravity inhibits the genetic expression of interleukin-2 and its receptor in mitogen-activated T lymphocytes. FEBS Lett. 1998;436:115-118.
34. Hammond TG, Lewis FC, Goodwin TJ, et al. Gene expression in space. Nat Med. 1999;5:359.
35. Stein GS, van Wijnen AJ, Stein JL, et al. Implications for interrelationships between nuclear architecture and control of gene expression under microgravity conditions. FASEB J. 1999;13:157-166.
36. Margolis L, Hatfill S, Chuaqui R, et al. Long term organ culture of human prostate tissue in a NASA-designed rotating wall bioreactor. J Urol. 1999;161:290-297.
37. Akins RE, Schroedl NA, Gonda SR, et al. Neonatal rat heart cells cultured in simulated microgravity. In Vitro Cell Dev Biol Anim. 1997;33:337-343.
38. Zanjani ED, Pallavicini MG, Ascensao JL, et al. Engraftment and long-term expression of human fetal hematopoietic stem cells in sheep following transplantation in utero. J Clin Invest. 1992;89:1178-1188.
39. Civin CI, Almeida-Porada G, Lee M-J, Olweus J, Terstappen LWMM, Zanjani ED. Sustained, retransplantable, multilineage engraftment of highly purified adult human bone marrow stem cells in vivo. Blood. 1996;88:4102-4109.
40. Yin AH, Miragi AS, Zanjani ED, et al. AC133, A novel marker for human hematopoietic stem and progenitor cells. Blood. 1997;90:5002-5012.
41. Shimizu Y, Ogawa M, Kobayashi M, Almeida-Porada G, Zanjani ED. Engraftment of cultured human hematopoietic cells in sheep. Blood. 1998;91:3688-3692.
42. + cells. Exp Hematol. 1998;26:353-360.
43. Giesert C, Almeida-Porada G, Scheffold A, Kanz L, Zanjani ED, Buhring HJ. The monoclonal antibody W7C5 defines a novel surface antigen on hematopoietic stem cells. Ann N Y Acad Sci. 2001;938:175-183.
44. + cells from bone marrow. Exp Hematol. 2000;28:1071-1079.
45. Almeida-Porada G, Hoffman R, Manalo P, et al. Detection of human cells in human/sheep chimeric lambs with in vitro human stroma-forming potential. Exp Hematol. 1996;24:482-487.
46. +/- cells in vivo [abstract]. Blood. 2000;96:494a.
47. Almeida-Porada G, Crapnell K, Porada C, et al. Transplantation of human neuronal stem cells into fetal sheep give rise to hematopoietic cells in vivo [abstract]. Blood. 1999;94:129a.
48. Almeida-Porada G, Crapnell K, Porada C, et al. In vivo hematopoietic potential of human neuronal stem cells. Exp Hematol. 2000;28:61a.
49. Reyes M, Lund T, Lenvik T, Aguiar D, Koodie L, Verfaillie CM. Purification and ex vivo expansion of postnatal human marrow mesodermal progenitor cells. Blood. 2000;98:2615-2625.
50. Liechty KW, MacKenzie, TC, Shaaban AF, et al. Human mesenchymal stem cells engraft and demonstrate site-specific differentiation after in utero transplantation in sheep. Nat Med. 2000;6:1282-1286.
51. Kopen GC, Prockop DJ, Phinney DG. Marrow stromal cells migrate throughout forebrain and cerebellum, and they differentiate into astrocytes after injection into neonatal mouse brains. Proc Natl Acad Sci U S A. 1999;96:10711-10716.
52. Sanchez-Ramos J, Song S, Cardozo-Pelaez F, et al. Adult bone marrow stromal cells differentiate into neural cells in vitro. Exp Neurol. 2000;164:247-256.
53. Woodbury D, Schwarz EJ, Prockop DJ, Black IB. Adult rat and human bone marrow stromal cells differentiate into neurons. J Neurosci Res. 2000;61:364-370.
54. Pittenger MF, Mackay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284:143-147.
55. Mackay AM, Beck SC, Murphy JM, Barry FP, Chichester CO, Pittenger MF. Chondrogenic differentiation of cultured human mesenchymal stem cells from marrow. Tissue Eng. 1998;4:415-428.
56. Almeida-Porada G, Porada C, El Shabrawy D, Simmons PJ, Zanjani ED. Human marrow stromal cells (MSC) represent a latent pool of stem cells capable of generating long-term hematopoietic cells [abstract]. Blood. 2001;98:713a.
57. Almeida-Porada G, El Shabrawy D, Porada C, Ascensao JL, Zanjani ED. Clonally derived marrow stromal cells (MSC) populations are able to differentiate into blood, liver and skin cells [abstract]. Blood. 2001;98:791a.
58. Wang X, Willenbring H, Akkari Y, et al. Cell fusion is the principal source of bone-marrow-derived hepatocytes. Nature. 2003;422:897-901.