Advertisement
Research Article Free access | 10.1172/JCI115498
Department of Anatomy, University of California, San Francisco 94143-0452.
Find articles by Huang, K. in: JCI | PubMed | Google Scholar
Department of Anatomy, University of California, San Francisco 94143-0452.
Find articles by Geoffroy, J. in: JCI | PubMed | Google Scholar
Department of Anatomy, University of California, San Francisco 94143-0452.
Find articles by Singer, M. in: JCI | PubMed | Google Scholar
Department of Anatomy, University of California, San Francisco 94143-0452.
Find articles by Rosen, S. in: JCI | PubMed | Google Scholar
Published November 1, 1991 - More info
Lymphocytes enter lymph nodes by first adhering to high endothelial venules, an adhesive event mediated by a lectinlike lymphocyte receptor (L-selectin). Previously, it was shown with an in vitro assay that lymphocytes preferentially adhere to myelin-rich regions in brain sections. Here, using a recombinant form of L-selectin as an immunohistochemical reagent, we demonstrate potential ligands for L-selectin in myelinated regions of the central but not the peripheral nervous system. Using several antibodies and phorbol ester downmodulation of the receptor, we establish that L-selectin on human lymphocytes has a primary involvement in lymphocyte adherence to the myelinated regions. On mouse lymphocytes, the contribution of L-selectin appears to be partial. These findings raise the possibility that leukocyte targeting to myelin-rich regions, via a L-selectin dependent mechanism, may be a factor in the pathogenesis of certain central nervous system demyelinating diseases.
Images.