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Antigen-Independent Maturation of CD2, CD11a/CD18, CD44, and CD58 Expression on Thymic Emigrants in Fetal and Postnatal Sheep

Identifieur interne : 00D414 ( Main/Curation ); précédent : 00D413; suivant : 00D415

Antigen-Independent Maturation of CD2, CD11a/CD18, CD44, and CD58 Expression on Thymic Emigrants in Fetal and Postnatal Sheep

Auteurs : Deborah A. Witherden [Australie] ; Nevin J. Abernethy [France] ; Wayne G. Kimpton [Nouvelle-Zélande] ; Ross N. P. Cahill [Nouvelle-Zélande]

Source :

RBID : PMC:2275959

Abstract

We have compared the expression of CD2, CD11a/CD18, CD44, and CD58 on αβ and γδT cells emigrating from the fetal and postnatal thymus. We report that both γδ and the CD4+ CD8- and CD4-CD8+ subsets of αβ T cells express mature levels of the adhesion molecules CD11a/CD18, CD44, and CD58 upon emigration from the thymus. Whereas CD44 is up-regulated on γδ+ thymocytes prior to export, down-regulation of both CD11a/CD18 and CD58 occurs prior to emigration from the thymus, suggesting that down-regulation of these molecules may be a final maturational step taken by developing γδ T cells before their export from the thymus. In contrast, there is continued up-regulation of CD2 on αβ and γδ T cells upon emigration from the thymus and as they move into the mature peripheral T-cell pool. There was also a marked reduction in the number of CD2+γδ T cells exported during fetal development that was associated with a marked reduction in the percentage of CD22+ γδ thymocytes exported. The postthymic maturation of CD2 and the other changes in adhesion-molecule expression appear to be independent of extrinsic antigen, as the same changes were observed in the antigen-free environment of the fetus as in the postnatal lamb, which has been exposed to extrinsic antigen. It thus appears that these changes in adhesion-molecule expression are as a result of the normal maturation pathway from a developing thymocyte to a mature peripheral T cell.


Url:
DOI: 10.1155/1995/35075
PubMed: 8770559
PubMed Central: 2275959

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PMC:2275959

Le document en format XML

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<addr-line>The University of Melbourne</addr-line>
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<name sortKey="Abernethy, Nevin J" sort="Abernethy, Nevin J" uniqKey="Abernethy N" first="Nevin J." last="Abernethy">Nevin J. Abernethy</name>
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<p>We have compared the expression of CD2, CD11a/CD18, CD44, and CD58 on
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T cells emigrating from the fetal and postnatal thymus. We report that both
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CD8
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and CD4
<sup>-</sup>
CD8
<sup>+</sup>
subsets of
<italic>αβ</italic>
T cells express mature levels of the adhesion molecules CD11a/CD18, CD44, and CD58 upon emigration from the thymus. Whereas CD44 is up-regulated on
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thymocytes prior to export, down-regulation of both CD11a/CD18 and CD58 occurs prior to emigration from the thymus, suggesting that down-regulation of these molecules may be a final maturational step taken by developing
<italic>γδ</italic>
T cells before their export from the thymus. In contrast, there is continued up-regulation of CD2 on
<italic>αβ</italic>
and
<italic>γδ</italic>
T cells upon emigration from the thymus and as they move into the mature peripheral T-cell pool. There was also a marked reduction in the number of CD2
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<italic>γδ</italic>
T cells exported during fetal development that was associated with a marked reduction in the percentage of CD2
<sup>2+</sup>
<italic>γδ</italic>
thymocytes exported. The postthymic maturation of CD2 and the other changes in adhesion-molecule expression appear to be independent of extrinsic antigen, as the same changes were observed in the antigen-free environment of the fetus as in the postnatal lamb, which has been exposed to extrinsic antigen. It thus appears that these changes in adhesion-molecule expression are as a result of the normal maturation pathway from a developing thymocyte to a mature peripheral T cell.</p>
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