Telen M J
Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Transfus Clin Biol. 1995;2(4):291-301. doi: 10.1016/s1246-7820(05)80095-3.
The Lutheran (Lu) blood group antigens are a family of human erythrocyte antigens which reside on two closely-related erythrocyte integral membrane proteins. Sixteen Lutheran or so-called para-Lutheran antigens have thus far been described, and human antisera to many of them have been shown to immunoblot two proteins, of 78 and 85 kDa. Lu cDNA encodes an integral membrane protein of 597 amino acids that is a member of the Ig superfamily. Lu proteins comprise five Ig superfamily domains, along with a single transmembrane domain and a cytoplasmic domain of about 60 amino acids. The two proteins seen in biochemical studies of red cell membranes appear to be derived from 2 mRNA species that differ only in their 3' ends, suggesting that they arise from alternate splicing of a single preRNA. Three genetic backgrounds for the Lu(a-b-) [Lu null] phenotype have been described. A recessive Lu null phenotype is rarely observed as a result of homozygosity for two amorphic LU alleles. However, the most common Lu(a-b-) phenotype appears to be caused by an independently segregating, dominant gene, designated In (Lu), which inhibits expression of all Lutheran antigens to nearly undetectable levels. This gene also affects the expression of other cell surface proteins and blood group antigens that are genetically unlinked to the Lutheran locus, including CD44 and MER2. CD44, a member of the cartilage link family of proteins, bears the In and AnWj blood group antigens. A widely distributed protein CD44 is expressed at normal levels on all tissues except erythrocytes in the presence of the In (Lu) gene. A second Lutheran regulatory gene, XS2, is responsible for the third Lu(a-b-) phenotype, which exhibits an X-linked inheritance pattern. The XS2 gene down-regulates but does not abolish expression of LU genes and does not affect expression of CD44.
路德(Lu)血型抗原是人类红细胞抗原家族,存在于两种密切相关的红细胞整合膜蛋白上。迄今为止,已描述了16种路德或所谓的类路德抗原,并且已证明针对其中许多抗原的人抗血清可免疫印迹出78 kDa和85 kDa的两种蛋白质。Lu cDNA编码一个由597个氨基酸组成的整合膜蛋白,该蛋白是免疫球蛋白超家族的成员。Lu蛋白包含五个免疫球蛋白超家族结构域,以及一个单一的跨膜结构域和一个约60个氨基酸的胞质结构域。在红细胞膜的生化研究中看到的这两种蛋白质似乎源自两种仅在3'末端不同的mRNA种类,这表明它们是由单个前体RNA的可变剪接产生的。已描述了Lu(a-b-)[Lu缺失]表型的三种遗传背景。由于两个无定形LU等位基因的纯合性,隐性Lu缺失表型很少见。然而,最常见的Lu(a-b-)表型似乎是由一个独立分离的显性基因In(Lu)引起的,该基因将所有路德抗原的表达抑制到几乎无法检测的水平。该基因还影响其他细胞表面蛋白和与路德基因座遗传不连锁的血型抗原的表达,包括CD44和MER2。CD44是软骨连接蛋白家族的成员,带有In和AnWj血型抗原。在存在In(Lu)基因的情况下,广泛分布的蛋白CD44在除红细胞外的所有组织中均以正常水平表达。第二个路德调节基因XS2负责第三种Lu(a-b-)表型,该表型表现出X连锁遗传模式。XS2基因下调但不消除LU基因的表达,并且不影响CD44的表达。