Distribution of CD31 on CD4 T-Cells from Cord Blood, Peripheral Blood and Tonsil at Different Stages of Differentiation
Raul Ruiz-Hernandez1, Antoni Jou2, Cecilia Cabrera1, Ferdinand Noukwe1, Josep deHaro3, Francesc Borras4, Julia Blanco1, Marco Fernandez5, Bonaventura Clotet1, Lidia Ruiz1, Margarita Bofill*, 1, 6
Identifiers and Pagination:Year: 2010
First Page: 19
Last Page: 26
Publisher Id: TOIJ-3-19
Article History:Received Date: 24/11/2009
Revision Received Date: 18/12/2009
Acceptance Date: 24/12/2009
Electronic publication date: 5/3/2010
Collection year: 2010
open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
CD31+ is a marker for recent thymic emigrants. Nevertheless it is present in a proportion of memory cells. We looked at the distribution of CD31 on CD4 T-cell subpopulations. In cord blood, CD31 was present in the majority of the CD45RAhighhigh and 60% of the CD45RAlow cells, and in adults over 70% of “true” naive and in 5 - 10% of all memory subpopulations (central memory, effector memory, follicular helper and T regulatory cells). No major differences were seen in the distribution of chemokine receptors between CD31+ and CD31 - populations within the näive cells nor the memory populations except for CCR3 and CCR9, which were preferentially expressed in the CD31+ memory cells. The CD31 distribution and cytokine receptors was similar between HIV negative and positive individuals, and between adult blood and tonsils. There was a correlation between the levels of TRECs and the percentages of CD31 in all samples studied.