Literature DB >> 4050973

Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. I. Quantitative histopathology; PMN, basophil, and mononuclear cell survival; and unbound (serum) protein content.

A M Dannenberg, P J Pula, L H Liu, S Harada, F Tanaka, R F Vogt, A Kajiki, K Higuchi.   

Abstract

When applied topically to the skin of rabbits in vivo, sulfur mustard (SM), the vesicant used in World War I, produced a slowly developing inflammatory response, which peaked in size at 1 and 2 days, ulcerated within 3 days, and reepithelialized by 10 days. Histologically, basophils and polymorphonuclear leukocytes (PMNs) were common in both early and late lesions, and the crust over the ulcers was composed of dead epidermal cells, fibrin, and large numbers of PMNs. Healing occurred under the crust by migration of epidermal cells from the margins of the lesions and from the hair follicles. In organ culture, the lesion explants survived well, and reepithelialization even took place. Their excellent survival enabled us to compare the life spans of the infiltrating leukocytes within an inflammatory site. PMNs within the explants began disappearing during the first day of culture, and almost all had disappeared by 3 days. In contrast, over half of the basophils and the mononuclear cells within the explants were still present after 3 days of culture. The 1-, 2-, 3-, 6-, and 10-day (1.0-sq cm) SM lesion biopsies showed a 30-45% increase in weight (when compared with normal skin), presumably due to the extravasation of serum proteins and the fluids retained by them. When the biopsies were organ-cultured for 3 days, the 1-, 2-, and 3-day lesions lost weight, and the 6- and 10-day lesions (and normal skin) gained weight. These weight differences were not due to the amount of unbound protein extractable into the culture fluids, because both the early lesions and the late lesions contained about the same amount of unbound protein. The most likely explanation for these weight differences is that the newly formed ground substances of late lesions absorbed culture fluid, because the ground substance had changed from the sol state of acute inflammation (in which it was extractable) back to its normal gel state (in which it was not extractable). The unbound protein extractable into the culture fluids was mostly of serum origin. This protein averaged 1.9 mg for 1.0 sq cm normal skin explants (with a mean weight of 215 mg), and 6.4 mg for 1-day SM lesions (with a mean weight of 313 mg). Because rabbit serum contains about 60 mg protein/ml, these figures indicate that normal skin contained about 15% (unbound) serum by weight.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 4050973      PMCID: PMC1888029     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  24 in total

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Authors:  S L James; D G Colley
Journal:  J Reticuloendothel Soc       Date:  1975-11

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Authors:  E P BEAVEN; A J COX
Journal:  J Invest Dermatol       Date:  1965-03       Impact factor: 8.551

3.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

Review 4.  Cell-to-cell interactions in the secretion of enzymes of connective tissue breakdown, collagenase and proteoglycan-degrading neutral proteases. A review.

Authors:  G Vaes
Journal:  Agents Actions       Date:  1980-12

5.  The artificial granuloma 1: in vitro lymphokine production by pulmonary artificial hypersensitivity granulomas.

Authors:  L Carrick; D L Boros
Journal:  Clin Immunol Immunopathol       Date:  1980-11

Review 6.  Protein inhibitors of proteinases.

Authors:  M Laskowski; I Kato
Journal:  Annu Rev Biochem       Date:  1980       Impact factor: 23.643

7.  The secretion of migration inhibitory factor by intact schistosome egg granulomas maintained in vitro.

Authors:  D L Boros; K S Warren; R P Pelley
Journal:  Nature       Date:  1973-11-23       Impact factor: 49.962

8.  The effect of synovial tissue on the breakdown of articular cartilage in organ culture.

Authors:  H B Fell; R W Jubb
Journal:  Arthritis Rheum       Date:  1977 Sep-Oct

9.  The pathogenic role of pemphigus antibodies and proteinase in epidermal acantholysis.

Authors:  S Morioka; K Naito; H Ogawa
Journal:  J Invest Dermatol       Date:  1981-05       Impact factor: 8.551

10.  Hepatic fibrosis in schistosomiasis: egg granulomas secrete fibroblast stimulating factor in vitro.

Authors:  D J Wyler; S M Wahl; L M Wahl
Journal:  Science       Date:  1978-10-27       Impact factor: 47.728

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  14 in total

1.  Two-compartment model for rabbit skin organ culture.

Authors:  A A Rutten; B G Béquet-Passelecq; H B Koëter
Journal:  In Vitro Cell Dev Biol       Date:  1990-04

2.  Electron microscopic study of guinea pig skin exposed to sulphur mustard.

Authors:  R S Chauhan; L V Murthy; S C Pant
Journal:  Bull Environ Contam Toxicol       Date:  1995-07       Impact factor: 2.151

3.  Chemotactic factors released in culture by intact developing and healing skin lesions produced in rabbits by the irritant sulfur mustard.

Authors:  F Tanaka; A M Dannenberg; K Higuchi; M Nakamura; P J Pula; T E Hugli; R G Discipio; D L Kreutzer
Journal:  Inflammation       Date:  1997-04       Impact factor: 4.092

4.  Sulfur mustard induced mast cell degranulation in mouse skin is inhibited by a novel anti-inflammatory and anticholinergic bifunctional prodrug.

Authors:  Laurie B Joseph; Gabriella M Composto; Roberto M Perez; Hong-Duck Kim; Robert P Casillas; Ned D Heindel; Sherri C Young; Carl J Lacey; Jaya Saxena; Christophe D Guillon; Claire R Croutch; Jeffrey D Laskin; Diane E Heck
Journal:  Toxicol Lett       Date:  2017-11-07       Impact factor: 4.372

5.  Effect of sulphur mustard on mouse skin--an electron microscopic evaluation.

Authors:  R S Chauhan; L V Murthy; R C Malhotra
Journal:  Bull Environ Contam Toxicol       Date:  1993-09       Impact factor: 2.151

6.  Proteases released in organ culture by acute dermal inflammatory lesions produced in vivo in rabbit skin by sulfur mustard: hydrolysis of synthetic peptide substrates for trypsin-like and chymotrypsin-like enzymes.

Authors:  K Higuchi; A Kajiki; M Nakamura; S Harada; P J Pula; A L Scott; A M Dannenberg
Journal:  Inflammation       Date:  1988-08       Impact factor: 4.092

7.  Expression of proliferative and inflammatory markers in a full-thickness human skin equivalent following exposure to the model sulfur mustard vesicant, 2-chloroethyl ethyl sulfide.

Authors:  Adrienne T Black; Patrick J Hayden; Robert P Casillas; Diane E Heck; Donald R Gerecke; Patrick J Sinko; Debra L Laskin; Jeffrey D Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2010-09-16       Impact factor: 4.219

8.  Inflammatory mediators and modulators release in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. II. Evans blue dye experiments that determined the rates of entry and turnover of serum protein in developing and healing lesions.

Authors:  S Harada; A M Dannenberg; A Kajiki; K Higuchi; F Tanaka; P J Pula
Journal:  Am J Pathol       Date:  1985-10       Impact factor: 4.307

Review 9.  Mechanisms mediating the vesicant actions of sulfur mustard after cutaneous exposure.

Authors:  Michael P Shakarjian; Diane E Heck; Joshua P Gray; Patrick J Sinko; Marion K Gordon; Robert P Casillas; Ned D Heindel; Donald R Gerecke; Debra L Laskin; Jeffrey D Laskin
Journal:  Toxicol Sci       Date:  2009-10-15       Impact factor: 4.849

10.  Toxic effects of sulfur mustard on respiratory epithelial cells in culture.

Authors:  M Chevillard; P Lainee; P Robineau; E Puchelle
Journal:  Cell Biol Toxicol       Date:  1992 Apr-Jun       Impact factor: 6.691

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