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Updated: Jan 7, 2026

Ex vivo Imaging of T Cells in Murine Lymph Node Slices with Widefield and Confocal Microscopes
Published on: July 15, 2011
IL-7 promotes naïve T cell motility to enable T cell scanning of dendritic cells in the LN
Janie R Byrum1, Kimberly A Morrissey1, David J Torres2
1Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, MSC 08 4660, 1 University of New Mexico, Albuquerque, NM 87131, USA.
Abstract:
IL-7 is a key regulator of naïve T cell homeostasis including T cell development, survival, and proliferation. IL-7 is highly expressed in lymph nodes (LNs), and we investigated the potential for IL-7 to drive naïve T cell movement in LNs. We show that IL-7 can mediate high speed T cell movement in vitro and in LNs. Downstream of IL-7R, T cell motility requires JAK1/3 and STAT5 activation, but mTOR signaling is not required. Using computational modeling and imaging of T cell motion in lymph nodes through two photon microscopy, we find that IL-7R-mediated motility accounts for T cell localization near DCs in the LN, suggesting that IL-7 can regulate naive T cell contacts with DCs. These data demonstrate a novel role for the IL-7/IL-7R pathway in controlling rapid T cell motility, showing that IL-7/IL-7R mediated T cell motion can facilitate efficient T cell-DC interactions in the LN.
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