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Updated: Jul 7, 2026

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
Published on: June 22, 2016
[Inhibitory Effect of CCL20 on CD4+ CD25+ regulatory T cell development in mouse thymus]
Xian-An Shao1, Fu-Hua Yuang, Yong Wang
1Centre of Clinical Molecular Medicine, PLA 123 Hospital, Bengbu 233015, Anhui Province, China. XAshao@126.com
Insights
Chemokine CCL20 plays a crucial role in the development of CD4(+)CD25(+) thymocytes. Interfering with CCL20 significantly downregulates these cells, offering insights into regulatory T cell development.
Area of Science:
- Immunology
- Developmental Biology
- Cell Biology
Context:
- Investigating the role of chemokine CCL20 in thymocyte development.
- Utilizing fetal thymus organ culture for in vitro studies.
- Analyzing thymocyte phenotypes using flow cytometry.
Purpose:
- To elucidate the function of chemokine CCL20 in the differentiation of CD4(+)CD25(+) thymocytes.
- To compare in vitro thymocyte development with in vivo processes.
- To assess the impact of CCL20 interference on CD4(+)CD25(+) T cell populations.
Summary:
- Fetal mouse thymus lobes cultured in vitro demonstrated developmental patterns of CD4(+)CD25(+) thymocytes mirroring in vivo development.
- Interference with chemokine CCL20 led to a significant decrease in the percentage of CD4(+)CD25(+) T cells.
- These findings suggest CCL20 is vital for the development of CD4(+)CD25(+) thymocytes.
Impact:
- Provides a better understanding of the development of naturally arising CD4(+)CD25(+) regulatory T cells.
- Highlights the regulatory role of CCL20 in T cell differentiation within the thymus.
- Offers potential targets for modulating immune responses.
Abstract:
The aim of this study was to investigate the roles of chemokine CCL20 in development of CD4(+)CD25(+) thymocytes by means of fetal thymus organ culture. Fetal mouse thymus lobes were removed at the fetus age of 14.5 days and cultured in complete RPMI 1640 with 20% FBS in vitro. Phenotypes of the thymocytes were analyzed by FACS and the number of cells per lobe was counted. The results revealed that from day 14.5 to day 19, the absolute and relative numbers of the CD4(+)CD25(+) thymocytes varied similarly as their development as in vitro culture at 6 days. Data showed that during the 6 days in vitro culture the CD4(+)CD25(+) cell percentage out of CD4(+) cells was 58.29%, 12.14%, 6.08%, 17.78%, 9.06%, 4.04% and the CD4(+)CD25(+) cell percentage out of CD25(+) cells was 3.75%, 10.81%, 17.20%, 51.93%, 61.64%, 80.06%. All these data indicated similar characters to their development in vivo. Moreover, at interference with CCL20, the percentage of CD4(+)CD25(+) T cells in thymocytes significantly decreased at the 3 and 6 days from 3.24+/-0.18 and 3.96+/-0.24 to 1.27+/-0.11 (p<0.001) and 1.76+/-0.22 (p<0.001) respectively. It is concluded that the development of CD4(+)CD25(+) thymocytes is similar both in vitro and in vivo, interfering with CCL20 significantly downregulate the expression of CD4(+)CD25(+) T cells. The above data may help to understand the development of naturally arising CD4(+)CD25(+) regulatory T cells.
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