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International Immunology, Vol. 14, No. 6, pp. 545-554, June 2002
© 2002 Japanese Society for Immunology

Human macrophage lectin specific for galactose/N-acetylgalactosamine is a marker for cells at an intermediate stage in their differentiation from monocytes into macrophages

Nobuaki Higashi1, Akiko Morikawa1, Kouki Fujioka1, Yuko Fujita1, Yoshihiko Sano1, Megumi Miyata-Takeuchi1, Noriko Suzuki1 and Tatsuro Irimura1

1 Laboratory of Cancer Biology and Molecular Immunology, Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Correspondence to: T. Irimura; E-mail: irimura{at}mol.f.u-tokyo.ac.jp
Transmitting editor: S. Koyasu

We studied the expression of a human macrophage lectin specific for galactose/N-acetylgalactosamine (hMGL) during macrophage differentiation. The expression of hMGL during the in vitro differentiation induced by human serum was examined by immunostaining and Western blotting with a specific mAb, MLD-1, as well as with RT-PCR analysis. hMGL was detected on cells at an intermediate stage of differentiation. These cells were round, slightly larger in size (12.7 ± 0.2 µm) than monocytes (9.8 ± 0.1 µm) and expressed the macrophage marker CD14, but lacked the dendritic cell marker CD1a. The highest levels of expression occurred after 2–4 days of culture. At this time point, MLD-1 prominently stained 20–40% of the cells. Monocytes cultured for 16 h or fully differentiated monocyte-derived macrophages were negative or weak for hMGL expression. Similar transient expression was also observed during granulocyte macrophage colony stimulating factor- or macrophage colony stimulating factor-dependent macrophage differentiation. The lectin was characterized as a functional endocytic receptor for glycosylated macromolecules, since the uptake of carbohydrate polymers was partially inhibited by the addition of MLD-1. The distribution of hMGL+ cells in normal human skin was found by immunostaining to be mainly in the upper dermis distant from vascular structures. More than 90% of the hMGL+ cells were double stained with anti-CD68 mAb and constituted ~20% of the CD68+ cells. We suggest that the dermal hMGL+ cells are a subset of differentiated cells derived from monocytes and that hMGL is a unique marker for cells at an intermediate stage of macrophage differentiation.

Keywords: C-type lectin, dendritic cells, differentiation, endocytosis, macrophages, skin


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