Koike R, Watanabe T, Satoh H, Hee C S, Kitada K, Kuramoto T, Serikawa T, Miyawaki S, Miyasaka M
First Department of Internal Medicine, Tokyo Medical and Dental University, Japan.
Cell Immunol. 1997 Aug 25;180(1):62-9. doi: 10.1006/cimm.1997.1177.
The aly, alymphoplasia, is an autosomal recessive mutation in mice of an unknown etiology, which induces total aplasia of lymph nodes and Peyer's patches. We hypothesized that the lack of lymphoid tissue may be due to abnormalities of lymphocyte traffic into these tissues. Therefore, we analyzed the expression of various adhesion molecules associated with lymphocyte homing. Among the adhesion molecules examined, all were normally expressed except the mucosal addressin MAdCAM-1. In aly/aly mice MAdCAM-1 was absent in the spleen at mRNA and protein levels, but was normally expressed in the intestinal venules. The FISH analysis and linkage analysis using microsatellite markers demonstrated that the MAdCAM-1 gene is located on chromosome 10, indicating that MAdCAM-1 is not encoded by the aly gene, which is located on chromosome 11. Our results indicate that the aberrant expression of MAdCAM-1 is not the direct cause of aly mutation but rather a secondary defect.
aly(无淋巴细胞症)是一种病因不明的小鼠常染色体隐性突变,它会导致淋巴结和派伊尔结完全发育不全。我们推测淋巴组织的缺失可能是由于淋巴细胞向这些组织迁移异常所致。因此,我们分析了与淋巴细胞归巢相关的各种黏附分子的表达情况。在所检测的黏附分子中,除黏膜地址素MAdCAM - 1外,其他均正常表达。在aly/aly小鼠中,脾脏中MAdCAM - 1在mRNA和蛋白质水平均缺失,但在肠小静脉中正常表达。荧光原位杂交(FISH)分析以及使用微卫星标记的连锁分析表明,MAdCAM - 1基因位于10号染色体上,这表明MAdCAM - 1并非由位于11号染色体上的aly基因编码。我们的结果表明,MAdCAM - 1的异常表达不是aly突变的直接原因,而是一种继发性缺陷。