Isolation and characterization of naïve follicular dendritic cells

• Published in: Molecular immunology Vol. 50; no. 3; pp. 172 - 176
• Main Authors: Usui, Kenta, Honda, Shin-ichiro, Yoshizawa, Yuichi, Nakahashi-Oda, Chigusa, Tahara-Hanaoka, Satoko, Shibuya, Kazuko, Shibuya, Akira
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.03.2012; Elsevier
• Subjects: Animals; B-Cell Activating Factor - immunology; B-Lymphocytes - immunology; BAFF (B cell activating factor TNF family); Cell Culture Techniques - methods; Cell Proliferation; Cell Separation - methods; dendritic cells; Dendritic Cells, Follicular - cytology; FDCs (follicular dendritic cells); flow cytometry; functional properties; humoral immunity; Mice; Mice, Inbred C57BL; neutralizing antibodies; spleen; splenocytes; tumor necrosis factors; FDCs (follicular dendritic cells); BAFF (B cell activating factor TNF family)
• ISSN: 0161-5890; 1872-9142; 1872-9142
• DOI: 10.1016/j.molimm.2011.11.010

► We established a novel method for FDC isolation from the spleen of naïve mice. ► Naïve FDC is can be isolated as by sorting CD45−, FDC-M2+ and ICAM-1+ cells from the spleen by flow cytometry. ► Isolated FDC supported B cells proliferation via BAFF. Follicular dendritic cells (FDC) are specialized antigen-presenting cells to cognate B cells in the follicle of the lymphoid tissues. FDC also support survival and proliferation of the B cells, leading to the germinal center formation. FDC therefore play a central role in humoral immune responses. However, molecular and functional characteristics of FDC are largely unknown, because it is difficult to isolate and analyze FDC due to a very small number of FDC in the lymphoid tissues and the fragility by mechanical and chemical stresses in vitro. In this report, we established a novel method for FDC isolation from the spleen of naïve mice by flow cytometry and analyzed the phenotypical and functional characteristics. The isolated FDC, which accounted for ∼0.2% of the spleen cells of naïve mice, were CD45−, FDC-M2+, and ICAM-1+, and supported the survival and LPS-induced proliferation of B cells. We also showed that a neutralizing antibody against B cell activating factor TNF family (BAFF) suppressed FDC-dependent B cell proliferation in the presence of LPS, but not survival, demonstrating the evidence that FDC-derived BAFF is involved in B cell proliferation.