Suppression of hematopoietic activity in tenascin-C-deficient mice

Blood

Volumn 91, Issue 11, 1998, Pages 4074-4083

  Ohta, Masatsugu ^a   Sakai, Takao ^b   Saga, Yumiko ^b   Aizawa, Shin Ichi ^b   Saito, Masaki ^b  

^a HOKKAIDO UNIVERSITY   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

TENASCIN;

ANIMAL CELL; ARTICLE; BONE MARROW CELL; CELL GROWTH; COLONY FORMATION; EXTRACELLULAR MATRIX; GENETIC RECOMBINATION; GROWTH INHIBITION; HEMATOPOIESIS; KNOCKOUT MOUSE; MONONUCLEAR CELL; MOUSE; NONHUMAN; ORGANOGENESIS; PRIORITY JOURNAL; PROTEIN FAMILY; PROTEIN PROTEIN INTERACTION; STEM CELL;

ANIMALS; CELLS, CULTURED; COLONY-FORMING UNITS ASSAY; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HEMATOPOIESIS; HEMATOPOIETIC STEM CELLS; MICE; MICE, INBRED C57BL; MICE, INBRED CBA; MICE, KNOCKOUT; STROMAL CELLS; TENASCIN;

EID: 0032100451     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (50)

1. Gordon MY: Extracellular matrix of the marrow microenvironment. Br J Haematol 70:1, 1988
2. Torok-Storb B: Cellular interactions. Blood 72:373, 1988
3. Russell ES: Hereditary animals of the mouse: A review for geneticists. Adv Genet 20:357, 1979
4. Silvers WK: Steel, flexed-tailed, splotch, and varitint-waddler, in: The Coat Colors of Mice: A Model for Mammalian Gene Action and Interaction. New York, NY, Springer-Verlag, 1979, p 243
5. d) deficient in response to erythropoietin. Ann NY Acad Sci 149:475, 1968
6. d. Blood 26:399, 1965
7. Chabot B, Stephenson DA, Chapman VM, Besmer P, Berstein A: The protooncogene c-kit endoding a transmembrane tyrosine kinase receptor maps to the mouse W locus. Nature 335:88, 1988
8. Geissler EN, Ryan MA, Housman DE: The dominant-white spotting (W) locus of the mouse encodes the c-kit protooncogene. Cell 55:185, 1988
9. Willams DE, Eisenman J, Baird A, Rauch C, Van Ness K, March CJ, Park LS, Martin U, Mochizuki DY, Boswell HS, Burgess GS, Cosman D, Lyman SD: Identification of a ligand for the c-kit proto-oncogene. Cell 63:167, 1990
10. Copeland NG, Gilbert DJ, Cho BC, Donovan PJ, Jenkins NA, Cosman D, Anderson D, Lyman SD, Williams DE: Mast cell growth factor maps near the Steel locus on mouse chromosome 10 and is deleted in a number of Steel alleles. Cell 63:175, 1990
11. Matthews W, Jordan CT, Wiegand GW, Paardoll D, Lemischka IR: A receptor tyrosine kinase specific to hematopoietic stem and progenitor cell-enriched populations. Cell 65:1143, 1991
12. Rosnet O, Marchetto S, deLapeyriere O, Birnbaum D: Murine Flt3, a gene encoding a novel tyrosine kinase receptor of the PDGFR/CSF1R family. Oncogene 6:1641, 1991
13. Lyman SD, James L, Bos TV, de Vries P, Brasel K, Gliniak B, Hollingsworth LT, Picha KS, McKenna HJ, Splett RR, Fletcher FA, Maraskovsky E, Farrah T, Foxworthe D, Williams DE, Beckmann MP: Molecular cloning of a ligand for the flt3/flk-2 tyrosine kinase receptor: A proliferative factor for primitive hematopoietic cells. Cell 75:1157, 1993
14. Mackarehtschian K, Hardin JD, Moore KA, Boast S, Goff SP, Lemischka IR: Targeted disruption of the flk2/flt3 gene leads to deficiencies in primitive hematopoietic progenitors. Immunity 3:147, 1995
15. Shalaby F, Rossant J, Yamaguchi TP, Gertsenstein M, Wu X-F, Breitman ML, Schuh AC: Failure of blood-island formation and vasculogenesis in flk-1-deficient mice. Nature 376:62, 1995
16. Wu H, Liu X, Jaenisch R, Lodish HF: Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor. Cell 83:59, 1995
17. Robb L, Drinkwater CC, Metcalf D, Li R, Köntgen F, Nicola N, Begley G: Hematopoietic and lung abnormalities in mice with a null mutation of the common β subunit of the receptors for granulocyte-macrophage colony-stimulating factor and interleukins 3 and 5. Proc Natl Acad Sci USA 92:9565, 1995
18. Derynck R: TGF-β-receptor-mediated signaling. Trends Biochem Sci 19:548, 1994
19. Ohta M, Greenberger JS, Anklesaria P, Bassols A, Massagué, J: Two forms of transforming growth factor-β distinguished by multipotential haematopoietic progenitor cells. Nature 329:539, 1987
20. Oshima M, Shima H, Taketo MM: TGF-β receptor type II deficiency results in defects of yolk sac hematopoiesis and vasculogenesis. Develop Biol 179:297, 1996
21. Dickson MC, Martin JS, Cousins FM, Kulkarni AB, Karlsson S, Akhurst RJ: Defective haemopoiesis and vasculogenesis in transfroming growth factor-β1 knock out mice. Development 121:1845, 1995
22. Broxmeyer HE, Sherry BS, Lu L, Cooper S, Oh K-O, Tekamp-Olson T, Kwon BS, Cerami A: Enhancing and suppressing effects of recombinant murine macrophage inflammatory proteins on colony formation in vitro by bone marrow myeloid progenitor cells. Blood 76:1110, 1990
23. Cook DN, Beck MA, Coffman TM, Kirby SL, Sheridan JF, Pragnell IB, Smithies O: Requirement of MIP-1α for an inflammatory response to viral infection. Science 269:1583, 1995
24. Hirsch E, Iglesias A, Potocnik AJ, Hartmann U, Fässler R: Impaired migration but not differentiation of hematopoietic stem cells in the absence of β1 integrins. Nature 380:171, 1996
25. Arroyo AG, Yang JT, Rayburn H, Hynes RO: Differential requirements for α4 integrins during fetal and adult hematopoiesis. Cell 85:997, 1996
26. Donehower LA, Harvey M, Slagle BL, McArthur MJ, Montgomery CA Jr, Butel JS, Bradley A: Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours. Nature 356:215, 1992
27. George EL, Georges-Labouesse EN, Patel-King RS, Rayburn H, Hynes RO: Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin. Development 119:1079, 1993
28. Sakai T, Ohta M, Kawakatsu H, Furukawa Y, Saito M: Tenascin-C induction in Whitlock-Witte culture: A relevant role of the thiol moiety in lymphoid-lineage differentiation. Exp Cell Res 217:395, 1995
29. Chiquet-Ehrismann R, Mackie EJ, Pearson CA, Sakakura T: Tenascin: An extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis. Cell 47:131, 1986
30. Erickson HP: Tenascin-C, tenascin-R, and tenascin-X: A family of talented proteins in search of functions. Curr Opin Cell Biol 5:869, 1993
31. Erickson HP, Bourdon MA: Tenascin: An extracellular matrix protein prominent in specialized embryonic tissues and tumors. Annu Rev Cell Biol 5:71, 1989
32. Matsumoto K-I, Saga Y, Ikemura T, Sakakura T, Chiquet-Ehrismann R: The distribution of Tenascin-X is distinct and often reciprocal to that of tenascin-C. J Cell Biol 125:483, 1994
33. Rathjen FG, Wolff JM, Chiquet-Ehrismann R: Restrictin: A chick neural extracellular matrix protein involved in cell attachment copurifies with the cell recognition molecules F11. Development 113:151, 1991
34. Saga Y, Yagi T, Ikawa Y, Sakakura T, Aizawa S: Mice develop normally without tenascin. Gene Dev 6:1821, 1992
35. Forsberg E, Hirsch E, Frohlich L, Meyer M, Ekblom P, Aszodi A, Werner S, Fassler R: Skin wounds and severed nerves heal normally in mice lacking tenascin-C. Proc Natl Acad Sci USA 93:6594, 1996
36. Dexter TM, Allen TD, Lajtha LG: Conditions controlling the proliferation of hematopoietic stem cells in vitro. J Cell Physiol 91:335, 1977
37. Ohta M, Anklesaria P, Wheaton M, Ohara A, Pierce JH, Holland CA, Greenberger JS: Retroviral src gene expression in continuous marrow culture increases the self-renewal capacity of multilineage hematopoietic stem cells. Leukemia 3:206, 1989
38. Greenberger JS: Sensitivity of corticosteroid-dependent, insulin-resistant lipogenesis in marrow preadipocytes of mutation diabetic-obese mice. Nature 275:752, 1978
39. Whitlock CA, Robertson D, Witte ON: Murine B cell lymphopoiesis in long term culture. J Immunol Methods 67:353, 1984
40. Anklesaria P, Klassen V, Sakakeeny MA, FitzGerald TJ, Harrison D, Rybak ME, Greenberger JS: Biological characterization of cloned permanent stromal cell lines from anemic Sl/Sld mice and +/+ littermates. Exp Hematol 15:636, 1987
41. Kincade PW, Lee G, Paige CJ, Scheid MP: Cellular interactions affecting the maturation of murine B lymphocyte precursors in vitro. J Immunol 127:255, 1981
42. Till JE, McCulloch EA: A direct measurement of the radiation sensitivity of normal mouse bone marrow. Radiat Res 14:213, 1961
43. Oike Y, Hiraiwa H, Kawakatsu H, Nishikai M, Okinaka T, Suzuki T, Okada A, Yatani R, Sakakura T: Isolation and characterization of human fibroblast tenascin. An extracellular matrix glycoprotein of interest for developmental studies. Int J Dev Biol 34:309, 1990
44. Ekblom M, Fässler R, Tomasini-Johansson B, Nilsson K, Ekblom P: Downregulation of tenascin expression by glucocorticoids in bone marrow stromal cells and in fibroblasts. J Cell Biol 123:1037, 1993
45. Klein G, Beck S, Müller CA: Tenascin is a cytoadhesive extracellular matrix component of the human hematopoietic microenvironment. J Cell Biol 123:1027, 1993
46. Hemesath TJ, Stefansson K: Expression of tenascin in thymus and thymic nonlymphoid cells. J Immunol 152:422, 1994
47. Ocklind G, Talts J, Fässler R, Mattsson A, Ekblom P: Expression of tenascin in developing and adult mouse lymphoid organs. J Histchem Cytochem 41:1163, 1993
48. Tsai S, Patel V, Beaumont E, Lodish HF, Nathan DG, Sieff CA: Differential binding of erythroid and myeloid progenitors to fibroblasts and fibronectin. Blood 69:1587, 1987
49. Weinstein R, Riordan MA, Wenc K, Kreczko S, Zhou M, Dainiak N: Dual role of fibronectin in hematopoietic differentiation. Blood 73:111, 1989
50. Gordon MY, Riley GP, Watt SM, Greaves MF: Compartmentalization of a haematopoietic growth factor (GM-CSF) by glycosaminoglycans in the bone marrow microenvironment. Nature 326:403, 1987