Blood-derived small Dot cells reduce scar in wound healing

Experimental Cell Research

Volumn 314, Issue 7, 2008, Pages 1529-1539

  Kong, Wuyi ^a   Li, Shaowei ^a   Longaker, Michael T ^a   Lorenz, H Peter ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Blood derived; E cadherin; Integrin 1; Stem cells; Transplantation; Wound healing

Indexed keywords

ATAXIN 1; BETA1 INTEGRIN; CD31 ANTIGEN; CD34 ANTIGEN; CD45 ANTIGEN; HERMES ANTIGEN; MICROSOMAL AMINOPEPTIDASE; STEM CELL FACTOR RECEPTOR; UVOMORULIN;

ANIMAL EXPERIMENT; ARTICLE; CELL ISOLATION; CELL MIGRATION; CELL PROLIFERATION; CELL TRANSPLANTATION; CONTROLLED STUDY; FEMALE; IN VITRO STUDY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCAR; SKIN CELL; WOUND HEALING;

MUS;

EID: 40949147340     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yexcr.2008.01.022     Document Type: Article

References (41)

1. Adzick N.S., Harrison M.R., Glick P.L., Beckstead J.H., Villa R.L., Scheuenstuhl H., and Goodson III W.H. Comparison of fetal, newborn, and adult wound healing by histologic, enzyme-histochemical, and hydroxyproline determinations. J. Pediatr. Surg. 20 (1985) 315-319
2. Longaker M.T., Whitby D.J., Adzick N.S., Crombleholme T.M., Langer J.C., Duncan B.W., Bradley S.M., Stern R., Ferguson M.W., and Harrison M.R. Studies in fetal wound healing, VI. Second and early third trimester fetal wounds demonstrate rapid collagen deposition without scar formation. J. Pediatr. Surg. 25 (1990) 63-86 discussion 68-9
3. Lorenz H.P., and Adzick N.S. Scarless skin wound repair in the fetus. West. J. Med. 159 (1993) 350-355
4. Soo C., Beanes S.R., Hu F.Y., Zhang X., Dang C., Chang G., Wang Y., Nishimura I., Freymiller E., Longaker M.T., Lorenz H.P., and Ting K. Ontogenetic transition in fetal wound transforming growth factor-beta regulation correlates with collagen organization. Am. J. Pathol. 163 (2003) 2459-2476
5. Jones P.H., and Watt F.M. Separation of human epidermal stem cells from transit amplifying cells on the basis of differences in integrin function and expression. Cell 73 (1993) 713-724
6. Rendl M., Lewis L., and Fuchs E. Molecular dissection of mesenchymal-epithelial interactions in the hair follicle. PLoS Biol. 3 (2005) e331
7. Tumbar T., Guasch G., Greco V., Blanpain C., Lowry W.E., Rendl M., and Fuchs E. Defining the epithelial stem cell niche in skin. Science 303 (2004) 359-363
8. Levy V., Lindon C., Harfe B.D., and Morgan B.A. Distinct stem cell populations regenerate the follicle and interfollicular epidermis. Dev. Cell 9 (2005) 855-861
9. Trempus C.S., Morris R.J., Bortner C.D., Cotsarelis G., Faircloth R.S., Reece J.M., and Tennant R.W. Enrichment for living murine keratinocytes from the hair follicle bulge with the cell surface marker CD34. J. Invest. Dermatol. 120 (2003) 501-511
10. Yang A., Kaghad M., Caput D., and McKeon F. On the shoulders of giants: p63, p73 and the rise of p53. Trends Genet. 18 (2002) 90-95
11. Toma J.G., McKenzie I.A., Bagli D., and Miller F.D. Isolation and characterization of multipotent skin-derived precursors from human skin. Stem Cells 23 (2005) 727-737
12. Medina R.J., Kataoka K., Takaishi M., Miyazaki M., and Huh N.H. Isolation of epithelial stem cells from dermis by a three-dimensional culture system. J. Cell. Biochem. 98 (2006) 174-184
13. Shizuru J.A., Negrin R.S., and Weissman I.L. Hematopoietic stem and progenitor cells: clinical and preclinical regeneration of the hematolymphoid system. Annu. Rev. Med. 56 (2005) 509-538
14. Wagers A.J., Christensen J.L., and Weissman I.L. Cell fate determination from stem cells. Gene Ther. 9 (2002) 606-612
15. Ferrari G., Cusella-De Angelis G., Coletta M., Paolucci E., Stornaiuolo A., Cossu G., and Mavilio F. Muscle regeneration by bone marrow-derived myogenic progenitors. Science 279 (1998) 1528-1530
16. Mezey E., Chandross K.J., Harta G., Maki R.A., and McKercher S.R. Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow. Science 290 (2000) 1779-1782
17. Lagasse E., Connors H., Al-Dhalimy M., Reitsma M., Dohse M., Osborne L., Wang X., Finegold M., Weissman I.L., and Grompe M. Purified hematopoietic stem cells can differentiate into hepatocytes in vivo. Nat. Med. 6 (2000) 1229-1234
18. Sata M., Saiura A., Kunisato A., Tojo A., Okada S., Tokuhisa T., Hirai H., Makuuchi M., Hirata Y., and Nagai R. Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. Nat. Med. 8 (2002) 403-409
19. Wagers A.J., Sherwood R.I., Christensen J.L., and Weissman I.L. Little evidence for developmental plasticity of adult hematopoietic stem cells. Science 297 (2002) 2256-2259
20. Balsam L.B., Wagers A.J., Christensen J.L., Kofidis T., Weissman I.L., and Robbins R.C. Haematopoietic stem cells adopt mature haematopoietic fates in ischaemic myocardium. Nature 428 (2004) 668-673
21. Roybon L., Ma Z., Asztely F., Fosum A., Jacobsen S.E., Brundin P., and Li J.Y. Failure of transdifferentiation of adult hematopoietic stem cells into neurons. Stem Cells 24 (2006) 1594-1604
22. Jiang Y., Jahagirdar B.N., Reinhardt R.L., Schwartz R.E., Keene C.D., Ortiz-Gonzalez X.R., Reyes M., Lenvik T., Lund T., Blackstad M., Du J., Aldrich S., Lisberg A., Low W.C., Largaespada D.A., and Verfaillie C.M. Pluripotency of mesenchymal stem cells derived from adult marrow. Nature 418 (2002) 41-49
23. D'Ippolito G., Diabira S., Howard G.A., Menei P., Roos B.A., and Schiller P.C. Marrow-isolated adult multilineage inducible (MIAMI) cells, a unique population of postnatal young and old human cells with extensive expansion and differentiation potential. J. Cell Sci. 117 (2004) 2971-2981
24. Kogler G., Sensken S., Airey J.A., Trapp T., Muschen M., Feldhahn N., Liedtke S., Sorg R.V., Fischer J., Rosenbaum C., Greschat S., Knipper A., Bender J., Degistirici O., Gao J., Caplan A.I., Colletti E.J., Almeida-Porada G., Muller H.W., Zanjani E., and Wernet P. A new human somatic stem cell from placental cord blood with intrinsic pluripotent differentiation potential. J. Exp. Med. 200 (2004) 123-135
25. Chiavegato A., Bollini S., Pozzobon M., Callegari A., Gasparotto L., Taiani J., Piccoli M., Lenzini E., Gerosa G., Vendramin I., Cozzi E., Angelini A., Iop L., Zanon G.F., Atala A., De Coppi P., and Sartore S. Human amniotic fluid-derived stem cells are rejected after transplantation in the myocardium of normal, ischemic, immuno-suppressed or immuno-deficient rat. J. Mol. Cell. Cardiol. 42 (2007) 746-759
26. Holden C. Stem cells. Controversial marrow cells coming into their own?. Science 315 (2007) 760-761
27. Rizvi A.Z., Swain J.R., Davies P.S., Bailey A.S., Decker A.D., Willenbring H., Grompe M., Fleming W.H., and Wong M.H. Bone marrow-derived cells fuse with normal and transformed intestinal stem cells. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 6321-6325
28. Zavadil J., and Bottinger E.P. TGF-beta and epithelial-to-mesenchymal transitions. Oncogene 24 (2005) 5764-5774
29. Nishida M., Kawai K., Tanaka M., Tegoshi T., and Arizono N. Expression of E-cadherin in human mast cell line HMC-1. APMIS 111 (2003) 1067-1074
30. Abbruscato T.J., and Davis T.P. Protein expression of brain endothelial cell E-cadherin after hypoxia/aglycemia: Influence of astrocyte contact. Brain Res. 842 (1999) 277-286
31. Borkowski T.A., Van Dyke B.J., Schwarzenberger K., McFarland V.W., Farr A.G., and Udey M.C. Expression of E-cadherin by murine dendritic cells: E-cadherin as a dendritic cell differentiation antigen characteristic of epidermal Langerhans cells and related cells. Eur. J. Immunol. 24 (1994) 2767-2774
32. Larue L., Ohsugi M., Hirchenhain J., and Kemler R. E-cadherin null mutant embryos fail to form a trophectoderm epithelium. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 8263-8267
33. Batlle E., Sancho E., Franci C., Dominguez D., Monfar M., Baulida J., and Garcia De Herreros A. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cells. Nat. Cell Biol. 2 (2000) 84-89
34. Boor P.J., and Ferrans V.J. Ultrastructural alterations in allylamine cardiovascular toxicity. Late myocardial and vascular lesions. Am. J. Pathol. 121 (1985) 39-54
35. Hu K., Wu C., Mars W.M., and Liu Y. Tissue-type plasminogen activator promotes murine myofibroblast activation through LDL receptor-related protein 1-mediated integrin signaling. J. Clin. Invest. 117 (2007) 3821-3832
36. Nagasawa T., Hirota S., Tachibana K., Takakura N., Nishikawa S., Kitamura Y., Yoshida N., Kikutani H., and Kishimoto T. Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1. Nature 382 (1996) 635-638
37. Mohle R., Bautz F., Rafii S., Moore M.A., Brugger W., and Kanz L. The chemokine receptor CXCR-4 is expressed on CD34+ hematopoietic progenitors and leukemic cells and mediates transendothelial migration induced by stromal cell-derived factor-1. Blood 91 (1998) 4523-4530
38. Lapidot T., Dar A., and Kollet O. How do stem cells find their way home?. Blood 106 (2005) 1901-1910
39. Schenk S., Mal N., Finan A., Zhang M., Kiedrowski M., Popovic Z., McCarthy P.M., and Penn M.S. Monocyte chemotactic protein-3 is a myocardial mesenchymal stem cell homing factor. Stem Cells 25 (2007) 245-251
40. Caussinus E., and Gonzalez C. Induction of tumor growth by altered stem-cell asymmetric division in Drosophila melanogaster. Nat. Genet. 37 (2005) 1125-1129
41. Pardal R., Clarke M.F., and Morrison S.J. Applying the principles of stem-cell biology to cancer. Nat. Rev., Cancer 3 (2003) 895-902