Spencer J, Hussell T, Mustafa Y, Perry M E
Department of Histopathology, UMDS, London, UK.
J Anat. 1996 Oct;189 ( Pt 2)(Pt 2):335-40.
Human lymphoma derived monoclonal antibody (anti "mucosal vessel associated antigen' [MVAA]) binds to high endothelial venules (HEV) in gut-associated lymphoid tissue, but shows only weak reactivity with HEV in peripheral lymphoid tissues. We have used immunohistochemistry and immunoelectron microscopy to define the precise ultrastructural distribution of the molecule, and to determine whether there is any association between this molecule and cellular traffic. We have observed that MVAA is a component of basement membrane which is only expressed by a subset of blood vessels. Although it is restricted to vessels which support lymphocyte traffic within lymphoid tissue, we did not observe any association between the distribution of MVAA and extravasating lymphocytes. MVAA is expressed in the fetal intestine in association with a subset of larger vessels. It is therefore not necessarily induced as a consequence of antigenic challenge. It is likely that MVAA has a structural role related to its restricted microanatomical distribution; possibly the maintenance of integrity of vessel walls which are continuously disrupted by the extravasation of lymphocytes.
人淋巴瘤衍生的单克隆抗体(抗“黏膜血管相关抗原”[MVAA])可与肠道相关淋巴组织中的高内皮微静脉(HEV)结合,但与外周淋巴组织中的HEV反应较弱。我们运用免疫组织化学和免疫电子显微镜技术来确定该分子精确的超微结构分布,并确定该分子与细胞迁移之间是否存在关联。我们观察到MVAA是基底膜的一个组成部分,仅由一部分血管表达。尽管它局限于支持淋巴组织内淋巴细胞迁移的血管,但我们并未观察到MVAA的分布与渗出淋巴细胞之间存在任何关联。MVAA在胎儿肠道中与一部分较大的血管相关表达。因此,它不一定是抗原刺激的结果。MVAA很可能因其有限的微观解剖分布而具有结构作用;可能是维持不断被淋巴细胞渗出破坏的血管壁的完整性。