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Human Follicular Dendritic Cells Express Prostacyclin Synthase: A Novel Mechanism to Control T Cell Numbers in the Germinal Center ¹

In Yong Lee^*,, Eun-Mi Ko^*,, Sang-Hyun Kim^*, Doo-Il Jeoung^, and Jongseon Choe^2,*,

^* Department of Microbiology and Immunology, Kangwon National University College of Medicine, and Vascular System Research Center, Kangwon National University, Chunchon, Kangwon, Republic of Korea; and Division of Life Sciences, Kangwon National University College of Natural Sciences, Chunchon, Kangwon, Republic of Korea

Stromal cells in the lymphoid organs provide a microenvironment where lymphocytes undergo various biological processes such as development, homing, clonal expansion, and differentiation. Follicular dendritic cells (FDCs) in the primary and secondary follicles of the peripheral lymphoid tissues interact with lymphocytes by contacting directly or producing diffusible molecules. To understand the biological role of human FDC at the molecular level, we developed a mAb, 3C8, that recognizes FDC but not bone marrow-derived cells. Through expression cloning and proteome analysis, we identified the protein that is recognized by 3C8 mAb, which revealed that FDC expresses prostacyclin synthase. The 3C8 protein purified from FDC-like cells indeed displayed the enzymatic activity of prostacyclin synthase and converted PGH₂ into prostacyclin. In addition, prostacyclin significantly inhibited proliferation of T cells but delayed their spontaneous apoptosis. These findings may help explain why T cells constitute only a minor population compared with B cells in the germinal center.

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