Proteomics demonstration that histone H4 is a colchicine-induced retro-modulator of growth and alkaline phosphatase activity in hair follicle dermal papilla culture

Journal of Proteomics

Volumn 74, Issue 6, 2011, Pages 805-816

  Hsia, Ching Wu ^a   Shui, Hao Ai ^b   Wang, Chih Yuan ^c   Yu, Hui Ming ^d   Ho, Ming Yi ^d   Cheng, Kur Ta ^a   Tseng, Min Jen ^e  

^a TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^b NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^d GENOMICS RESEARCH CENTER   (Taiwan)

^e NATIONAL CHUNG CHENG UNIVERSITY   (Taiwan)

Author keywords

Alopecia; Colchicine; Conditioned medium; Dermal papilla cell; Histone H4; Secretome

Indexed keywords

ALKALINE PHOSPHATASE; COLCHICINE; HISTONE H4; TRYPSIN;

ARTICLE; CELL CULTURE; CELL PROLIFERATION; CONTROLLED STUDY; DOWN REGULATION; GROWTH INHIBITION; HAIR DISEASE; HAIR FOLLICLE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; IN VIVO STUDY; MOLECULAR WEIGHT; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEOMICS; SKIN CELL; ULTRAFILTRATION; WESTERN BLOTTING;

ALKALINE PHOSPHATASE; ANIMALS; CELLS, CULTURED; COLCHICINE; DERMIS; HAIR FOLLICLE; HISTONES; RATS; VIBRISSAE;

EID: 79955477070     PISSN: 18743919     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jprot.2011.02.026     Document Type: Article

References (39)

1. Inamatsu M., Tochio T., Makabe A., Endo T., Oomizu S., Kobayashi E., et al. Embryonic dermal condensation and adult dermal papilla induce hair follicles in adult glabrous epidermis through different mechanisms. Dev Growth Differ 2006, 48:73-86.
2. Stenn K.S., Paus R. Controls of hair follicle cycling. Physiol Rev 2001, 81:449-494.
3. Schmidt-Ullrich R., Paus R. Molecular principles of hair follicle induction and morphogenesis. Bioessays 2005, 27:247-261.
4. Rosenquist T.A., Martin G.R. Fibroblast growth factor signaling in the hair growth cycle: expression of the fibroblast growth factor receptor and ligand genes in the murine hair follicle. Dev Dyn 1996, 205:379-386.
5. Schneider M.R., Schmidt-Ullrich R., Paus R. The hair follicle as a dynamic miniorgan. Curr Biol 2009, 19:R132-R142.
6. Botchkareva N.V., Ahluwalia G., Shander D. Apoptosis in the hair follicle. J Invest Dermatol 2006, 126:258-264.
7. Handjiski B.K., Eichmüller S., Hofmann U., Czarnetzki B.M., Paus R. Alkaline phosphatase activity and localization during the murine hair cycle. Br J Dermatol 1994, 131:303-310.
8. Hendrix S., Handjiski B., Peters E.M., Paus R. A guide to assessing damage response pathways of the hair follicle: lessons from cyclophosphamide-induced alopecia in mice. J Invest Dermatol 2005, 125:42-51.
9. Jahoda C.A. Induction of follicle formation and hair growth by vibrissa dermal papillae implanted into rat ear wounds: vibrissa-type fibres are specified. Development 1992, 115:1103-1109.
10. Weinberg W.C., Goodman L.V., George C., Morgan D.L., Ledbetter S., Yuspa S.H., et al. Reconstitution of hair follicle development in vivo: determination of follicle formation, hair growth, and hair quality by dermal cells. J Invest Dermatol 1993, 100:229-236.
11. Hastie S.B. Interactions of colchicine with tubulin. Pharmacol Ther 1991, 51:377-401.
12. Li Z., Davis G.S., Mohr C., Nain M., Gemsa D. Inhibition of LPS-induced tumor necrosis factor-alpha production by colchicine and other microtubule disrupting drugs. Immunobiology 1996, 195:624-639.
13. Harms M. Alopecia and hair changes following colchicine therapy. Hautarzt 1980, 31:161-163.
14. Ataş B., Caksen H., Tuncer O., Kirimi E., Akgün C., Odabaş D. Four children with colchicine poisoning. Hum Exp Toxicol 2004, 23:353-356.
15. Jahoda C.A., Oliver R.F. Vibrissa dermal papilla cell aggregative behaviour in vivo and in vitro. J Embryol Exp Morphol 1984, 79:211-224.
16. Matsuzaki T., Yoshizato K. Role of hair papilla cells on induction and regeneration processes of hair follicles. Wound Repair Regen 1998, 6:524-530.
17. Lü Z.F., Cai S.Q., Wu J.J., Zheng M. Biological characterization of cultured dermal stem cells and hair follicle regeneration in vitro and in vivo. Chin Med J (Engl) 2006, 119:275-281.
18. Foitzik K., Spexard T., Nakamura M., Halsner U., Paus R. Towards dissecting the pathogenesis of retinoid-induced hair loss: all-trans retinoic acid induces premature hair follicle regression (catagen) by upregulation of transforming growth factor-β2 in the dermal papilla. J Invest Dermatol 2005, 124:1119-1126.
19. Wolff J., Knipling L. Colchicine binding by the "isolated" beta-monomer of tubulin. J Biol Chem 1995, 270:16809-16812.
20. Kaidbey K.H. Hair growth inhibition as a method of screening drugs for local antimitotic activity. J Invest Dermatol 1977, 68:70-72.
21. Harris H. The human alkaline phosphatases: what we know and what we don't know. Clin Chim Acta 1990, 186:133-150.
22. Coburn S.P., Slominski A., Mahuren J.D., Wortsman J., Hessle L., Millan J.L. Cutaneous metabolism of vitamin B-6. J Invest Dermatol 2003, 120:292-300.
23. Berstine E.G., Hooper M.L., Grandchamp S., Ephrussi B. Alkaline phosphatase activity in mouse teratoma. Proc Natl Acad Sci USA 1973, 70:3899-3903.
24. Hahnel A.C., Rappolee D.A., Millan J.L., Manes T., Ziomek C.A., Theodosiou N.G., et al. Two alkaline phosphatase genes are expressed during early development in the mouse embryo. Development 1990, 110:555-564.
25. Sidhu K.S., Tuch B.E. Derivation of three clones from human embryonic stem cell lines by FACS sorting and their characterization. Stem Cells Dev 2006, 15:61-69.
26. Iida M., Ihara S., Matsuzaki T. Hair cycle-dependent changes of alkaline phosphatase activity in the mesenchyme and epithelium in mouse vibrissal follicles. Dev Growth Differ 2007, 49:185-195.
27. McElwee K.J., Kissling S., Wenzel E., Huth A., Hoffmann R. Cultured peribulbar dermal sheath cells can induce hair follicle development and contribute to the dermal sheath and dermal papilla. J Invest Dermatol 2003, 121:1267-1275.
28. Pemberton A.D., Brown J.K. In vitro interactions of extracellular histones with LDL suggest a potential pro-atherogenic role. PLoS ONE 2010, 5:e9884.
29. Pemberton A.D., Brown J.K., Inglis N.F. Proteomic identification of interactions between histones and plasma proteins: implications for cytoprotection. Proteomics 2010, 10:1484-1493.
30. Henriquez J.P., Casar J.C., Fuentealba L., Carey D.J., Brandan E. Extracellular matrix histone H1 binds to perlecan, is present in regenerating skeletal muscle and stimulates myoblast proliferation. J Cell Sci 2002, 115:2041-2051.
31. Mishra B., von der Ohe M., Schulze C., Bian S., Makhina T., Loers G., et al. Functional role of the interaction between polysialic acid and extracellular histone H1. J Neurosci 2010, 30:12400-12413.
32. Watabe Y., Kuramochi H., Furuya Y., Inagaki N., Seino S., Kimura S., et al. Identification of histone H2A.X as a growth factor secreted by an androgen-independent subline of mouse mammary carcinoma cells. J Biol Chem 1996, 271:25126-25130.
33. Cho J.H., Park I.Y., Kim H.S., Lee W.T., Kim M.S., Kim S.C. Cathepsin D produces antimicrobial peptide parasin I from histone H2A in the skin mucosa of fish. FASEB J 2002, 16:429-431.
34. Louters L.L., Henriksen E.J., Tipton C.M. Histone H4 stimulates glucose transport activity in rat skeletal muscle. Biochem J 1993, 295:549-553.
35. Louters L.L., Michele D.E., Pearson J.D. Histone H4 stimulates glucose uptake through the insulin receptor. Biochimie 1996, 78:39-45.
36. Hariton-Gazal E., Rosenbluh J., Graessmann A., Gilon C., Loyter A. Direct translocation of histone molecules across cell membranes. J Cell Sci 2003, 116:4577-4586.
37. Lee D.Y., Huang C.M., Nakatsuji T., Thiboutot D., Kang S.A., Monestier M., et al. Histone H4 is a major component of the antimicrobial action of human sebocytes. J Invest Dermatol 2009, 129:2489-2496.
38. Kleine T.J., Gladfelter A., Lewis P.N., Lewis S.A. Histone-induced damage of a mammalian epithelium: the conductive effect. Am J Physiol 1995, 268:C1114-C1125.
39. Xu J., Zhang X., Pelayo R., Monestier M., Ammollo C.T., Semeraro F., et al. Extracellular histones are major mediators of death in sepsis. Nat Med 2009, 15:1318-1321.