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Updated: Aug 23, 2026
Retroviral Overexpression of CXCR4 on Murine B-1a Cells and Adoptive Transfer for Targeted B-1a Cell Migration to the Bone Marrow and IgM Production
Published on: May 31, 2020
CXCR3 marks CD4+ memory T lymphocytes that are competent to migrate across a human brain microvascular endothelial
Melissa K Callahan1, Katherine A Williams, Pia Kivisäkk
1Department of Neurosciences, Cleveland Clinic Foundation, NC 30 Lerner Research Institute, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Abstract:
Chemokines and their receptors may be implicated in leukocyte ingress into brain during inflammation observed during the course of multiple sclerosis (MS). To address receptor modulation on CD4+ memory T lymphocytes during diapedesis, we used an in vitro model of the blood-brain barrier (BBB). We found that only memory (CD45RO+) cells transmigrated and type 3 CXC chemokine receptor (CXCR3) was enriched on transmigrated cells. CXCR3 depletion of the input population did not affect transmigration capability. CXCR3 reemerged on CXCR3 depleted cells independently of endothelial cell exposure, but was susceptible to incubation at 4 degrees C, indicating receptor recycling. We propose that CXCR3 serves as a surface marker for cells that have the capacity to cross the BBB, but does not play an essential role in extravasation.
