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Prepublished online as a Blood First Edition Paper on April 24, 2003; DOI 10.1182/blood-2003-03-0836.
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Blood, 1 September 2003, Vol. 102, No. 5, pp. 1678-1685
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
Impaired selectin-ligand biosynthesis and reduced inflammatory responses in -1,4-galactosyltransferase-Ideficient mice
Masahide Asano,
Susumu Nakae,
Norihiro Kotani,
Naoki Shirafuji,
Aya Nambu,
Noriyoshi Hashimoto,
Hiroto Kawashima,
Mayumi Hirose,
Masayuki Miyasaka,
Seiichi Takasaki, and
Yoichiro Iwakura
From the Department of Transgenic Animal Science, Graduate School of
Medical Science, Kanazawa University; Center for Experimental Medicine,
Department of Biochemistry, and Department of Advanced Medical Science,
Institute of Medical Science, University of Tokyo; and Laboratory of Molecular
and Cellular Recognition, Osaka University Graduate School of Medicine,
Japan.
Selectins recognize ligands containing carbohydrate chains such as sialyl
Lewis x (sLex) that are mainly presented at the terminus of
N-acetyl lactosamine repeats on core 2 O-glycans. Several
glycosyltransferases act successively to extend the N-acetyl
lactosamine repeats and to synthesize sLex, and
-1,4-galactosyltransferase ( 4GalT) plays a key role in these
processes. Recently isolated 6 4GalT genes are candidates, but
their individual roles, including those in selectin-ligand biosynthesis,
remain to be elucidated. More than 80% of the core 2 O-glycans on the
leukocyte membrane glycoproteins of 4GalT-Ideficient mice lacked
galactose residues in -1,4 linkage, and soluble P-selectin binding to
neutrophils and monocytes of these mice was significantly reduced, indicating
an impairment of selectin-ligand biosynthesis. 4GalT-Ideficient
mice exhibited blood leukocytosis but normal lymphocyte homing to peripheral
lymph nodes. Acute and chronic inflammatory responses, including the contact
hypersensitivity (CHS) and delayed-type hypersensitivity (DTH) responses, were
suppressed, and neutrophil infiltration into inflammatory sites was largely
reduced in these mice. Our results demonstrate that 4GalT-I is a major
galactosyltransferase responsible for selectin-ligand biosynthesis and that
inflammatory responses of 4GalT-Ideficient mice are impaired
because of the defect in selectin-ligand biosynthesis.

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