Learn D B, Snyder I S
Infect Immun. 1983 Feb;39(2):948-54. doi: 10.1128/iai.39.2.948-954.1983.
The reactivity of alveolar macrophages (AM) to cells and cell wall fractions (CWF) of Micropolyspora faeni was investigated. Exposure of cultured AM to M. faeni and its CWF caused the AM to form clumps or aggregates which remained attached to the culture dish surface. Other gram-positive and gram-negative bacteria as well as yeast, zymosan, latex microspheres, and isolated peptidoglycan from Listeria monocytogenes did not cause this response. The response was independent of species source and antibody content of the serum used in culture. The use of heat-inactivated sera negated the role of complement activation in the aggregation of AM. AM cultures required a period of culture before exposure to cells or CWF for this response to occur. This response was both time and dose dependent. Rabbit peritoneal macrophages also exhibited the clumping response. Degradation of a purified CWF, fraction 3, with lysozyme greatly diminished the clumping response. Chemical purification of fraction 3 with periodate, formamide, or trichloracetic acid also decreased this activity. These data suggest that the major active component causing this response is peptidoglycan but that other materials associated with the cell wall may also be important. A soluble-factor chemotactic for normal rabbit AM was found in the culture fluid of AM exposed to fraction 3. M. faeni cells and CWF also caused normal rabbit AM to chemiluminesce.
研究了肺泡巨噬细胞(AM)对微小多孢菌的细胞及细胞壁组分(CWF)的反应性。将培养的AM暴露于微小多孢菌及其CWF会导致AM形成团块或聚集体,并附着在培养皿表面。其他革兰氏阳性菌、革兰氏阴性菌以及酵母、酵母聚糖、乳胶微球和从单核细胞增生李斯特菌中分离出的肽聚糖均未引发这种反应。该反应与培养中所用血清的物种来源和抗体含量无关。使用热灭活血清消除了补体激活在AM聚集中的作用。AM培养物在暴露于细胞或CWF之前需要一段培养时间才能发生这种反应。这种反应具有时间和剂量依赖性。兔腹膜巨噬细胞也表现出聚集反应。用溶菌酶降解纯化的CWF组分3可大大减弱聚集反应。用高碘酸盐、甲酰胺或三氯乙酸对组分3进行化学纯化也会降低这种活性。这些数据表明,引起这种反应的主要活性成分是肽聚糖,但与细胞壁相关的其他物质可能也很重要。在暴露于组分3的AM培养液中发现了一种对正常兔AM有趋化作用的可溶性因子。微小多孢菌细胞和CWF也会使正常兔AM发生化学发光。