Expression of endogenous antimicrobial peptides in normal canine skin

Veterinary Dermatology - Tập 20 Số 1 - Trang 19-26 - 2009
Kyra V. Wingate1, Sheila M. F. Torres1, Kevin A.T. Silverstein2, Julie A. Hendrickson3, Mark S. Rutherford3
1Department of Veterinary Clinical Science, 1365 Gortner Avenue, 337 VMC, University of Minnesota, St. Paul, MN 55108, USA.
2Department of Plant Biology, 1445 Gortner Avenue, 250 BSC, University of Minnesota, St. Paul, MN 55108, USA
3Department of Veterinary and Biomedical Sciences, 1988 Fitch Avenue, 295 AS/VM, University of Minnesota, St. Paul, MN 55108, USA

Tóm tắt

Abstract

The cutaneous barrier contains small, cationic antimicrobial peptides that participate in the innate immunity against a wide variety of pathogens. Despite their immune importance, knowledge of canine defensins and their expression is limited primarily to testicular tissue and their relation to coat colour. Studies have shown that the absence of these antimicrobial peptides contribute to increased secondary infections in humans. The goals of this study were to identify defensin and protease inhibitor peptide genes by performing a computer‐based iterative screen of the canine genome and to determine whether antimicrobial peptides are expressed in normal canine skin. Reverse transcription‐polymerase chain reaction (RT‐PCR) was used to test for the expression of several antimicrobial peptides in the skin of five normal dogs. RNA from testis was used for comparison. The iterative screen identified 65 putative antimicrobial peptide genes on nine chromosomes, the majority clustered on chromosomes 16 and 24. Amplification of normal canine skin cDNAs demonstrated expression of antimicrobial peptide genes in five different body sites. These findings will provide a tool for future studies examining the association between antimicrobial gene expression and cutaneous immunity in dogs.

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Tài liệu tham khảo

10.1111/j.0022-202X.2004.23587.x

10.4049/jimmunol.174.8.4870

10.1038/35106587

10.1128/IAI.00524-06

10.1038/ni1206

10.1038/nri1180

10.1016/j.bbrc.2005.05.125

10.1042/BST0300111

Schalkwijk J, 1999, The trappin gene family: proteins defined by an N‐terminal transglutaminase substrate domain and a C‐terminal four‐disulphide core, The Biochemical Journal, 340, 569, 10.1042/bj3400569

10.1172/JCI118926

10.1111/j.1939-1676.2007.0038.x

10.1097/ACI.0b013e3282a64343

10.1128/IAI.73.5.2611-2620.2005

10.1016/j.dci.2007.03.007

10.1126/science.1147880

10.1093/bioinformatics/14.9.755

10.1111/j.1365-313X.2007.03136.x

10.1093/nar/29.1.159

10.1152/physiolgenomics.00104.2005

10.1042/CS20050115

10.1046/j.0022-202x.2001.01401.x

10.1074/jbc.272.33.20471

10.1007/s00335-005-0158-0

10.1007/s00335-005-0030-2

10.1128/IAI.69.4.2684-2691.2001

10.1038/sj.jid.5700861

10.1152/physiolgenomics.00113.2004

Alkemade JA, 1994, SKALP/elafin is an inducible proteinase inhibitor in human epidermal keratinocytes, Journal of Cell Science, 107, 2335, 10.1242/jcs.107.8.2335

10.1006/bbrc.1998.9069

10.1046/j.1523-1747.1998.00425.x