Mollicone R, Candelier J J, Mennesson B, Couillin P, Venot A P, Oriol R
INSERM U. 178, Villejuif, France.
Carbohydr Res. 1992 Apr 10;228(1):265-76. doi: 10.1016/s0008-6215(00)90564-0.
The use of synthetic trisaccharides as acceptors led to the definition of five main (1----3)-alpha-L-fucosyltransferase activity patterns in human adult tissues: (I). Myeliod cells, granulocytes, monocytes, and lymphoblasts, transfer an alpha-L-fucopyranosyl group to O-3 of a 2-acetamido-2-deoxy-D-glucosyl residue of H blood-group Type 2 oligosaccharide [alpha-L-Fucp-(1----2)-beta-D-Galp-(1----4)-beta-D-GlcpNAc----R] with Mn2+ as activator. (II) Brain has the same acceptor specificity pattern as myeloid cells, but can also use Co2+ as activator. (III) Plasma and liver transfer an alpha-L-furopyranosyl group to H blood-group Type 2 and to sialyl-N-acetyllactosamine [alpha-NeuAc-(2----3)-beta-D-Galp-(1----4)-beta-D-GlcpNAc----R]. (IV) Intestine, gall bladder, kidney, and milk have the same activity as (III), but also transfer an alpha-L-fucopyranosyl group to O-4 of a 2-acetamido-2-deoxy-D-glucose residue of H blood-group Type 1 [alpha-L-Fucp-(1----2)-beta-D-Galp-(1----3)-beta-D-GlcpNAc----R] and sialyl Type 1 [alpha-NeuAc-(1----3)-beta-D-Galp-(1----3)-beta-D-GlcpNAc----R]. (V) Stomach mucosa is not able to use sialyl-N-acetyllactosamine, but can transfer an alpha-L-fucopyranosyl group to the other Type 1 and Type 2 acceptors. Unlike in adult tissue, a single myeloid-like pattern of (1----3)-alpha-L-fucosyltransferase activity was found at early stages of development in all tissues tested. This embryonic enzyme is later progressively replaced by enzymes or mixtures of enzymes having the corresponding adult patterns of enzyme expression. All lymphoblastoid cell lines and half of the tumor epithelial cell lines tested expressed the myeloid-like pattern of enzyme found in normal embryonic tissues. The remaining tumor epithelial cell lines expressed different forms of (1----3/4)-alpha-L-fucosyltransferase acceptor specificity patterns.
使用合成三糖作为受体,确定了人类成人组织中五种主要的(1→3)-α-L-岩藻糖基转移酶活性模式:(I)髓样细胞、粒细胞、单核细胞和成淋巴细胞,以Mn2+作为激活剂,将一个α-L-岩藻吡喃糖基转移至H血型2型寡糖[α-L-Fucp-(1→2)-β-D-Galp-(1→4)-β-D-GlcpNAc→R]的2-乙酰氨基-2-脱氧-D-葡萄糖基残基的O-3位。(II)脑具有与髓样细胞相同的受体特异性模式,但也可使用Co2+作为激活剂。(III)血浆和肝脏将一个α-L-岩呋喃糖基转移至H血型2型寡糖和唾液酸化N-乙酰乳糖胺[α-NeuAc-(2→3)-β-D-Galp-(1→4)-β-D-GlcpNAc→R]。(IV)小肠、胆囊、肾脏和乳汁具有与(III)相同的活性,但也将一个α-L-岩吡喃糖基转移至H血型1型[α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc→R]和唾液酸化1型[α-NeuAc-(1→3)-β-D-Galp-(1→3)-β-D-GlcpNAc→R]的2-乙酰氨基-2-脱氧-D-葡萄糖残基的O-4位。(V)胃黏膜不能利用唾液酸化N-乙酰乳糖胺,但可将一个α-L-岩吡喃糖基转移至其他1型和2型受体。与成人组织不同,在所有测试组织的发育早期均发现单一的髓样样(1→3)-α-L-岩藻糖基转移酶活性模式。这种胚胎酶后来逐渐被具有相应成人酶表达模式的酶或酶混合物所取代。所有测试的淋巴母细胞系和一半的肿瘤上皮细胞系表达正常胚胎组织中发现的髓样样酶模式。其余的肿瘤上皮细胞系表达不同形式的(1→3/4)-α-L-岩藻糖基转移酶受体特异性模式。