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INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE

The cellular events in the ear skin and draining lymph node during the induction of contact sensitivity to 2-ethoxy methylene-5-oxazolone (oxazolone) have been studied in three strains of mice. The principal findings in the skin during the first 24 hr were invasion of polymorphs and destruction of p...

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Autores principales: de Sousa, Maria A. B., Parrott, Delphine M. V.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1969
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138717/
https://www.ncbi.nlm.nih.gov/pubmed/5343430
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author de Sousa, Maria A. B.
Parrott, Delphine M. V.
author_facet de Sousa, Maria A. B.
Parrott, Delphine M. V.
author_sort de Sousa, Maria A. B.
collection PubMed
description The cellular events in the ear skin and draining lymph node during the induction of contact sensitivity to 2-ethoxy methylene-5-oxazolone (oxazolone) have been studied in three strains of mice. The principal findings in the skin during the first 24 hr were invasion of polymorphs and destruction of pilosebaceous units, in both intact and thymectomized mice. Subsequently, the dermal cellular infiltrate increased and there was acanthosis of the epidermis. No lymphocytes were seen in the dermis or penetrating the epidermal basal cell layer in thymectomized mice. During the first 24 hr in the draining node, polymorphs and macrophages bearing a pigment with staining properties similar to melanin were seen in the marginal and medullary sinuses, in intact and thymectomized mice. Major differences, however, were revealed during 2–4 days when massive proliferation of large pyroninophilic blast cells occurred in the thymus-dependent area of the nodes from intact mice only. On testing, there was a prompt, measurable increase in ear thickness only in intact mice. This increase reached a peak at 24 hr — typical of a delayed type reaction. At testing, the ears from intact mice showed epidermal vesiculation and a considerable dermal cellular infiltrate with a substantial number of lymphocytes. This was in contrast with the completely quiescent appearance of the ear skin of thymectomized mice. Finally, we have discussed the use of the mouse as an experimental tool for studying contact sensitivity and have analyzed the role of the thymus-derived lymphocyte and the site where it becomes sensitized, in the light of current theory on the origin of cells and site where sensitization takes place in cell-mediated reactions.
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spelling pubmed-21387172008-04-17 INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE de Sousa, Maria A. B. Parrott, Delphine M. V. J Exp Med Article The cellular events in the ear skin and draining lymph node during the induction of contact sensitivity to 2-ethoxy methylene-5-oxazolone (oxazolone) have been studied in three strains of mice. The principal findings in the skin during the first 24 hr were invasion of polymorphs and destruction of pilosebaceous units, in both intact and thymectomized mice. Subsequently, the dermal cellular infiltrate increased and there was acanthosis of the epidermis. No lymphocytes were seen in the dermis or penetrating the epidermal basal cell layer in thymectomized mice. During the first 24 hr in the draining node, polymorphs and macrophages bearing a pigment with staining properties similar to melanin were seen in the marginal and medullary sinuses, in intact and thymectomized mice. Major differences, however, were revealed during 2–4 days when massive proliferation of large pyroninophilic blast cells occurred in the thymus-dependent area of the nodes from intact mice only. On testing, there was a prompt, measurable increase in ear thickness only in intact mice. This increase reached a peak at 24 hr — typical of a delayed type reaction. At testing, the ears from intact mice showed epidermal vesiculation and a considerable dermal cellular infiltrate with a substantial number of lymphocytes. This was in contrast with the completely quiescent appearance of the ear skin of thymectomized mice. Finally, we have discussed the use of the mouse as an experimental tool for studying contact sensitivity and have analyzed the role of the thymus-derived lymphocyte and the site where it becomes sensitized, in the light of current theory on the origin of cells and site where sensitization takes place in cell-mediated reactions. The Rockefeller University Press 1969-10-01 /pmc/articles/PMC2138717/ /pubmed/5343430 Text en Copyright © 1969 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
de Sousa, Maria A. B.
Parrott, Delphine M. V.
INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title_full INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title_fullStr INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title_full_unstemmed INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title_short INDUCTION AND RECALL IN CONTACT SENSITIVITY : CHANGES IN SKIN AND DRAINING LYMPH NODES OF INTACT AND THYMECTOMIZED MICE
title_sort induction and recall in contact sensitivity : changes in skin and draining lymph nodes of intact and thymectomized mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138717/
https://www.ncbi.nlm.nih.gov/pubmed/5343430
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