PMID- 25586548 OWN - NLM STAT- MEDLINE DCOM- 20151013 LR - 20181113 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 5 DP - 2015 Jan 14 TI - Concomitant analysis of Helios and Neuropilin-1 as a marker to detect thymic derived regulatory T cells in naive mice. PG - 7767 LID - 10.1038/srep07767 [doi] LID - 7767 AB - Regulatory T (Treg) cells are characterized by the expression of CD4, CD25 and the intracellular Foxp3. However, these markers do not indicate whether Treg cells are thymic derived Treg (tTreg) cells or peripherally induced Treg (pTreg) cells. Recently, Helios and Neuropilin-1 (Nrp1) has been reported as potential markers for tTreg cells. Herein, we used flow cytometry to examine the proportion of CD4(+)CD8(-)CD25(+) Treg cells expressing Helios, Nrp1 and Foxp3 in thymus, pancreatic draining lymph nodes (PDLNs) and spleen of CD-1 mice, and thymus of NOD and C57BL/6 mice. The frequency of Helios(+) cells was higher than that of Nrp1(+) cells in CD4(+)CD8(-)CD25(+) and CD4(+)CD8(-)CD25(+)Foxp3(+) Treg cells in thymus. Interestingly, the proportion of IL-10(+), Ebi3(+)and CTLA-4(+) cells was higher in Helios(+) than Nrp1(+) tTreg cells. The anti-apoptotic activity of Helios(+) tTreg cells was higher in thymus compared to Nrp1(+) tTreg cells. Nrp1 seems to be expressed at a later developmental stage compared to Helios and Foxp3. Furthermore, the expression of Nrp1 in CD4(+)CD25(+) T cells of younger mice did not increase after stimulating them in vitro with anti-CD3 and -CD28. Thus, under these conditions, Helios could be considered a more reliable marker for distinguishing tTreg cells from pTreg cells than Nrp1. FAU - Singh, Kailash AU - Singh K AD - Department of Medical Cell Biology, BMC, Uppsala University, Uppsala, Sweden. FAU - Hjort, Marcus AU - Hjort M AD - Department of Medical Cell Biology, BMC, Uppsala University, Uppsala, Sweden. FAU - Thorvaldson, Lina AU - Thorvaldson L AD - Department of Medical Cell Biology, BMC, Uppsala University, Uppsala, Sweden. FAU - Sandler, Stellan AU - Sandler S AD - Department of Medical Cell Biology, BMC, Uppsala University, Uppsala, Sweden. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20150114 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Biomarkers) RN - 0 (CTLA-4 Antigen) RN - 0 (DNA-Binding Proteins) RN - 0 (Ebi3 protein, mouse) RN - 0 (Minor Histocompatibility Antigens) RN - 0 (Receptors, Cytokine) RN - 0 (Transcription Factors) RN - 0 (Zfpn1a2 protein, mouse) RN - 130068-27-8 (Interleukin-10) RN - 144713-63-3 (Neuropilin-1) SB - IM MH - Animals MH - Apoptosis MH - Biomarkers/metabolism MH - CTLA-4 Antigen/metabolism MH - DNA-Binding Proteins/*metabolism MH - Interleukin-10/metabolism MH - Lymph Nodes/cytology MH - Lymphocyte Count MH - Male MH - Mice, Inbred C57BL MH - Mice, Inbred NOD MH - Minor Histocompatibility Antigens MH - Neuropilin-1/*metabolism MH - Receptors, Cytokine/metabolism MH - Spleen/cytology MH - T-Lymphocytes, Regulatory/*metabolism MH - Thymus Gland/*cytology MH - Transcription Factors/*metabolism PMC - PMC4293597 EDAT- 2015/01/15 06:00 MHDA- 2015/10/16 06:00 PMCR- 2015/01/14 CRDT- 2015/01/15 06:00 PHST- 2014/08/28 00:00 [received] PHST- 2014/12/16 00:00 [accepted] PHST- 2015/01/15 06:00 [entrez] PHST- 2015/01/15 06:00 [pubmed] PHST- 2015/10/16 06:00 [medline] PHST- 2015/01/14 00:00 [pmc-release] AID - srep07767 [pii] AID - 10.1038/srep07767 [doi] PST - epublish SO - Sci Rep. 2015 Jan 14;5:7767. doi: 10.1038/srep07767.