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SummaryLymphoid tissue inducer (LTi) cells have a well established role in secondary lymphoid tissue development. Here, we report on the heterogeneity of LTi cells based on their CD4 and chemokine receptor expression. The CD4− LTi‐cell population has a similar phenotype to the CD4+ population, with similar chemokine‐receptor‐expressing subsets. In both embryonic and adult spleen the CD4− LTi‐cell population is comparable as a proportion of total splenocytes to its CD4+ counterpart. In contrast, different proportions of CD4+ and CD4− LTi cells are found in different lymph nodes. Both CD4+ and CD4− LTi cells share the anatomical location and are associated with vascular cell adhesion molecule‐1‐positive stromal cells in spleen and lymph nodes. The numbers of both CD4+ and CD4− LTi cells in adult spleen are augmented in the presence of B cells. With the exception of CD4, there is a strong correlation coefficient (0·89) for gene expression between the two populations. Polymerase chain reaction analysis of individual CD4+ and CD4− LTi cells shows that a similar proportion in embryonic and adult spleen co‐expressed both CXCR5 and CCR7 or CXCR5 alone: 84·6% for adult CD4+ and 87·6% for adult CD4−; 95·3% for embryonic CD4+ and 91·5% for embryonic CD4−. Consistently fewer CCR7 single‐positive cells were found in the CD4+ and CD4− fractions in the embryo.

Original publication

DOI

10.1111/j.1365-2567.2007.02750.x

Type

Journal

Immunology

Publisher

Wiley

Publication Date

06/2008

Volume

124

Pages

166 - 174