Ezekowitz R A, Williams D J, Koziel H, Armstrong M Y, Warner A, Richards F F, Rose R M
Division of Hematology/Oncology, Children's Hospital, Boston, Massachusetts.
Nature. 1991 May 9;351(6322):155-8. doi: 10.1038/351155a0.
Human exposure to Pneumocystis carinii is common but, in the absence of acquired or genetic dysfunction of either cellular or humoral immunity, exposure rarely leads to illness. Although alveolar macrophages can degrade P. carinii, macrophage receptors involved in P. carinii recognition have not been clearly defined. Characterization of a predominant surface glycoprotein of the high mannose type led us to investigate the role of the macrophage mannose receptor in this process. We report here that binding and uptake of cultured rat P. carinii by human and rat alveolar macrophages is reduced by 90% in the presence of competitive inhibitors of mannose receptor activity and by adherence of alveolar macrophages to mannan-coated surfaces. Further, only those COS cells transfected with the human macrophage mannose receptor complementary DNA that express surface mannose receptors bind and ingest P. carinii. These studies establish that the macrophage mannose receptor is sufficient for uptake of P. carinii and emphasize the role of the alveolar macrophage in first-line host defence against P. carinii.
人类暴露于卡氏肺孢子菌的情况很常见,但在细胞免疫或体液免疫没有获得性或遗传性功能障碍的情况下,暴露很少导致疾病。虽然肺泡巨噬细胞可以降解卡氏肺孢子菌,但参与卡氏肺孢子菌识别的巨噬细胞受体尚未明确界定。一种主要的高甘露糖型表面糖蛋白的特性促使我们研究巨噬细胞甘露糖受体在此过程中的作用。我们在此报告,在存在甘露糖受体活性竞争性抑制剂的情况下,以及肺泡巨噬细胞黏附于甘露聚糖包被的表面时,人和大鼠肺泡巨噬细胞对培养的大鼠卡氏肺孢子菌的结合和摄取减少了90%。此外,只有那些转染了人类巨噬细胞甘露糖受体互补DNA并表达表面甘露糖受体的COS细胞才能结合并摄取卡氏肺孢子菌。这些研究表明,巨噬细胞甘露糖受体足以摄取卡氏肺孢子菌,并强调了肺泡巨噬细胞在宿主抵御卡氏肺孢子菌一线防御中的作用。