Temporal effects in porcine skin following bromine vapor exposure

References

• Sagi A, Baruchin AM, Ben-Yakar Y, Kon M, Eyal A, Mahler D. Burns caused by bromine and some of its compounds. Burns Incl Therm Inj 1985; 11(5):343–350.
   PubMedGoogle Scholar
• Dillman JF, III Hege, AI, Phillips CS, Orzolek LD, Sylvester AJ, Bossone C, Henemyre-Harris C, Kiser RC, Choi YW, Schlager JJ, Sabourin CL. Microarray analysis of mouse ear tissue exposed to bis-(2-chloroethyl) sulfide: gene expression profiles correlate with treatment efficacy and an established clinical endpoint. J Pharmacol Exp Ther 2006; 317(1):76–87.
   PubMed Web of Science ®Google Scholar
• McDougal JN, Garrett CM, Amato CM, Berberich SJ. Effects of brief cutaneous JP-8 jet fuel exposures on time course of gene expression in the epidermis. Toxicol Sci 2007; 95(2):495–510.
   PubMed Web of Science ®Google Scholar
• McDougal JN, Garrett CM. Gene expression and target tissue dose in the rat epidermis after brief JP-8 and JP-8 aromatic and aliphatic component exposures. Toxicol Sci 2007; 97(2):569–581.
   PubMed Web of Science ®Google Scholar
• Price JA, Rogers JV, McDougal JN, Shaw MQ, Reid FM, Kiser RC, Graham JS. Gene expression analysis of bromine-induced burns in porcine skin. Toxicol Lett 2008; 182(1-3):69–78.
   PubMed Web of Science ®Google Scholar
• Price JA, Rogers JV, McDougal JN, Shaw MQ, Reid FM, Graham JS. Transcriptional changes in porcine skin at 7 days following sulfur mustard and thermal burn injury. Cutan Ocul Toxicol 2009; 28(3):129–140.
   PubMed Web of Science ®Google Scholar
• Rogers JV, Garrett CM, McDougal JN. Gene expression in rat skin induced by irritating chemicals. J Biochem Mol Toxicol 2003; 17(3):123–137.
   PubMed Web of Science ®Google Scholar
• Rogers JV, Choi YW, Kiser RC, Babin MC, Casillas RP, Schlager JJ, Sabourin CL. Microarray analysis of gene expression in murine skin exposed to sulfur mustard. J Biochem Mol Toxicol 2004; 18(6):289–299.
   PubMed Web of Science ®Google Scholar
• Rogers JV, McDougal JN, Price JA, Reid FM, Graham JS. Transcriptional responses associated with sulfur mustard and thermal burns in porcine skin. Cutan Ocul Toxicol 2008; 27(3):135–160.
   PubMed Web of Science ®Google Scholar
• Rogers JV, Price JA, McDougal JN. A review of transcriptomics in cutaneous chemical exposure. Cutan Ocul Toxicol 2009; 28(4):157–70.
   PubMed Web of Science ®Google Scholar
• Rogers JV, Price JA, Shaw MQ, Reid F, Kiser RC, Graham JS. An Assessment of transcriptional changes in porcine skin exposed to bromine vapor. Journal of Biochemical and Molecular Toxicology 2010; In press.
   Web of Science ®Google Scholar
• Graham JS, Reid FM, Smith JR, Stotts RR, Tucker ES, Shumaker SM, Niemuth NA, Janny SJ. A cutaneous full-thickness liquid sulfur mustard burn model in weanling swine: clinical pathology and urinary excretion of thiodiglycol. J Appl Toxicol 2000; 20 Suppl 1:S161–S172.
   PubMedGoogle Scholar
• Graham JS, Schomacker KT, Glatter RD, Briscoe CM, Braue EH, Jr., Squibb KS. Efficacy of laser debridement with autologous split-thickness skin grafting in promoting improved healing of deep cutaneous sulfur mustard burns. Burns 2002; 28(8):719–730.
   PubMed Web of Science ®Google Scholar
• Graham JS, Stevenson RS, Mitcheltree LW, Simon M, Hamilton TA, Deckert RR, Lee RB. Improved wound healing of cutaneous sulfur mustard injuries in a weanling pig model. J Burns Wounds 2006; 5: e7.
   PubMedGoogle Scholar
• Reid FM, Graham J, Niemuth NA, Singer AW, Janny SJ, Johnson JB. Sulfur mustard-induced skin burns in weanling swine evaluated clinically and histopathologically. J Appl Toxicol 2000; 20 Suppl 1:S153–S160.
   PubMedGoogle Scholar
• Rice P, Brown RF, Lam DG, Chilcott RP, Bennett NJ. Dermabrasion–a novel concept in the surgical management of sulphur mustard injuries. Burns 2000; 26(1):34–40.
   PubMed Web of Science ®Google Scholar
• Perry MR, Reed B, Sparks G, Kiser RC, Reid FM, Graham JS. Bromine vapor cutaneous exposure system for weanling pigs. Toxicologist 2009; 108:S290.
   Google Scholar
• Curreri PW, Asch MJ, Pruitt BA. The treatment of chemical burns: specialized diagnostic, therapeutic, and prognostic considerations. J Trauma 1970; 10(8):634–642.
   PubMed Web of Science ®Google Scholar
• Kim IH, Seo SH. Occupational chemical burns caused by bromine. Contact Dermatitis 1999; 41(1):43.
   PubMed Web of Science ®Google Scholar
• Singer A, Sagi A, Ben MP, Rosenberg L. Chemical burns: our 10-year experience. Burns 1992; 18(3):250–252.
   PubMed Web of Science ®Google Scholar
• Enoch S, Grey JE, Harding KG. ABC of wound healing. Non-surgical and drug treatments. BMJ 2006; 332(7546):900–903.
   PubMed Web of Science ®Google Scholar
• DiPietro LA. Wound healing: the role of the macrophage and other immune cells. Shock 1995; 4(4):233–240.
   PubMed Web of Science ®Google Scholar
• Gillitzer R, Goebeler M. Chemokines in cutaneous wound healing. J Leukoc Biol 2001; 69(4):513–521.
   PubMed Web of Science ®Google Scholar
• Werner S, Grose R. Regulation of wound healing by growth factors and cytokines. Physiol Rev 2003; 83(3):835–870.
   PubMed Web of Science ®Google Scholar
• Wagener FA, van Beurden HE, von den Hoff JW, Adema GJ, Figdor CG. The heme-heme oxygenase system: a molecular switch in wound healing. Blood 2003; 102(2):521–528.
   PubMed Web of Science ®Google Scholar
• Hanselmann C, Mauch C, Werner S. Haem oxygenase-1: a novel player in cutaneous wound repair and psoriasis? Biochem J 2001; 353(Pt 3):459–466.
   PubMedGoogle Scholar
• Jazwa A, Loboda A, Golda S, Cisowski J, Szelag M, Zagorska A, Sroczynska P, Drukala J, Jozkowicz A, Dulak J. Effect of heme and heme oxygenase-1 on vascular endothelial growth factor synthesis and angiogenic potency of human keratinocytes. Free Radic Biol Med 2006; 40(7):1250–1263.
   PubMed Web of Science ®Google Scholar
• Kampfer H, Kolb N, Manderscheid M, Wetzler C, Pfeilschifter J, Frank S. Macrophage-derived heme-oxygenase-1: expression, regulation, and possible functions in skin repair. Mol Med 2001; 7(7):488–498.
   PubMed Web of Science ®Google Scholar
• Pae HO, Ae HY, Chai KY, Chung HT. Heme oxygenase-1 attenuates contact hypersensitivity induced by 2,4-dinitrofluorobenzene in mice. Immunopharmacol Immunotoxicol 2008; 30(2):207–216.
   PubMed Web of Science ®Google Scholar
• Listopad J, Asadullah K, Sievers C, Ritter T, Meisel C, Sabat R, Docke WD. Heme oxygenase-1 inhibits T cell-dependent skin inflammation and differentiation and function of antigen-presenting cells. Exp Dermatol 2007; 16(8):661–670.
   PubMed Web of Science ®Google Scholar
• Patil K, Bellner L, Cullaro G, Gotlinger KH, Dunn MW, Schwartzman ML. Heme oxygenase-1 induction attenuates corneal inflammation and accelerates wound healing after epithelial injury. Invest Ophthalmol Vis Sci 2008; 49(8):3379–3386.
   PubMed Web of Science ®Google Scholar
• Willis D, Moore AR, Frederick R, Willoughby DA. Heme oxygenase: a novel target for the modulation of the inflammatory response. Nat Med 1996; 2(1):87–90.
   PubMed Web of Science ®Google Scholar
• Tedder TF, Li X, Steeber DA. The selectins and their ligands: adhesion molecules of the vasculature. Adv Mol Cell Biol 1999; 28:65–111.
   Google Scholar
• Yukami T, Hasegawa M, Matsushita Y, Fujita T, Matsushita T, Horikawa M, Komura K, Yanaba K, Hamaguchi Y, Nagaoka T, Ogawa F, Fujimoto M, Steeber DA, Tedder TF, Takehara K, Sato S. Endothelial selectins regulate skin wound healing in cooperation with L-selectin and ICAM-1. J Leukoc Biol 2007; 82(3):519–531.
   PubMed Web of Science ®Google Scholar
• Nagaoka T, Kaburagi Y, Hamaguchi Y, Hasegawa M, Takehara K, Steeber DA, Tedder TF, Sato S. Delayed wound healing in the absence of intercellular adhesion molecule-1 or L-selectin expression. Am J Pathol 2000; 157(1):237–247.
   PubMed Web of Science ®Google Scholar
• Subramaniam M, Saffaripour S, Van De Water L, Frenette PS, Mayadas TN, Hynes RO, Wagner DD. Role of endothelial selectins in wound repair. Am J Pathol 1997; 150(5):1701–1709.
   PubMed Web of Science ®Google Scholar
• Lowry SF. Cytokine mediators of immunity and inflammation. Arch Surg 1993; 128(11):1235–1241.
   PubMed Web of Science ®Google Scholar
• Paquet P, Ribbens C, Pierard GE. Epidermal interleukin-8 and its receptor CXCR2 in drug-induced toxic epidermal necrolysis. Clin Exp Dermatol 2007; 32(6):728–732.
   PubMed Web of Science ®Google Scholar
• Gyulai R, Hunyadi J, Kenderessy-Szabo A, Kemeny L, Dobozy A. Chemotaxis of freshly separated and cultured human keratinocytes. Clin Exp Dermatol 1994; 19(4):309–311.
   PubMed Web of Science ®Google Scholar
• Michel G, Kemeny L, Peter RU, Beetz A, Ried C, Arenberger P, Ruzicka T. Interleukin-8 receptor-mediated chemotaxis of normal human epidermal cells. FEBS Lett 1992; 305(3):241–243.
   PubMed Web of Science ®Google Scholar
• Rennekampff HO, Hansbrough JF, Kiessig V, Dore C, Sticherling M, Schroder JM. Bioactive interleukin-8 is expressed in wounds and enhances wound healing. J Surg Res 2000; 93(1):41–54.
   PubMed Web of Science ®Google Scholar
• Tuschil A, Lam C, Haslberger A, Lindley I. Interleukin-8 stimulates calcium transients and promotes epidermal cell proliferation. J Invest Dermatol 1992; 99(3):294–298.
   PubMed Web of Science ®Google Scholar
• Blumenfeld I, Ullmann Y, Laufer D, Livne E. Enhancement of Burn Healing By Growth Factors and IL-8. Annals of Burns and Fire Disasters 2000; 13 (4): 220–225.
   Google Scholar
• Pastore S, Mascia F, Mariotti F, Dattilo C, Girolomoni G. Chemokine networks in inflammatory skin diseases. Eur J Dermatol 2004; 14(4):203–208.
   PubMed Web of Science ®Google Scholar
• Ali S, Palmer AC, Banerjee B, Fritchley SJ, Kirby JA. Examination of the function of RANTES, MIP-1alpha, and MIP-1beta following interaction with heparin-like glycosaminoglycans. J Biol Chem 2000; 275(16):11721–11727.
   PubMed Web of Science ®Google Scholar
• Stasikowska O, Wagrowska-Danilewicz M. Chemokines and chemokine receptors in glomerulonephritis and renal allograft rejection. Med Sci Monit 2007; 13(2):RA31–RA36.
   PubMed Web of Science ®Google Scholar
• Suresh P, Wanchu A. Chemokines and chemokine receptors in HIV infection: role in pathogenesis and therapeutics. J Postgrad Med 2006; 52(3):210–217.
   PubMed Web of Science ®Google Scholar
• Weber C, Weber KS, Klier C, Gu S, Wank R, Horuk R, Nelson PJ. Specialized roles of the chemokine receptors CCR1 and CCR5 in the recruitment of monocytes and T(H)1-like/CD45RO(+) T cells. Blood 2001; 97(4):1144–1146.
   PubMed Web of Science ®Google Scholar
• Kaesler S, Bugnon P, Gao JL, Murphy PM, Goppelt A, Werner S. The chemokine receptor CCR1 is strongly up-regulated after skin injury but dispensable for wound healing. Wound Repair Regen 2004; 12(2):193–204.
   PubMed Web of Science ®Google Scholar
• Canavese M, Altruda F, Silengo L. Therapeutic efficacy and immunological response of CCL5 antagonists in models of contact skin reaction. PLoS One 2010; 5(1):e8725.
   PubMedGoogle Scholar
• Cascieri MA, Springer MS. The chemokine/chemokine-receptor family: potential and progress for therapeutic intervention. Curr Opin Chem Biol 2000; 4(4):420–427.
   PubMed Web of Science ®Google Scholar
• Horuk R. BX471: a CCR1 antagonist with anti-inflammatory activity in man. Mini Rev Med Chem 2005; 5(9):791–804.
   PubMed Web of Science ®Google Scholar
• Lederman MM, Penn-Nicholson A, Cho M, Mosier D. Biology of CCR5 and its role in HIV infection and treatment. JAMA 2006; 296(7):815–826.
   PubMed Web of Science ®Google Scholar
• Machado RR, Soares DM, Proudfoot AE, Souza GE. CCR1 and CCR5 chemokine receptors are involved in fever induced by LPS (E. coli) and RANTES in rats. Brain Res 2007; 1161:21–31.
   PubMed Web of Science ®Google Scholar
• Pease JE, Horuk R. CCR1 antagonists in clinical development. Expert Opin Investig Drugs 2005; 14(7):785–796.
   PubMed Web of Science ®Google Scholar