Interaction of bacterial cell wall polymers and rat macrophages.

J H Schwab, R Smialowicz
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Abstract

Processing of group A and group D streptococcal cell wall was measured after phagocytosis by normal rat peritoneal cells in tissue culture. Group A cell wall was practically non-biodegradable in contrast to group D, which was over 80% degraded by 4-8 days in culture. There was no difference in elimination or degradation of mucopeptide or polysaccharide of group A cell walls. Neither antiserum or sensitized lymphocytes affected persistence. Macrophages from Fisher rats (susceptible to group A cell wall-induced polyarthritis) became cytotoxic for target L-cells 6-7 days after ingestion of group A cell walls. Phagocytosis of group D cell walls induced less cytotoxicity. Macrophages from Buffalo rats (resistant to polyarthritis) were less cytotoxic after phagocytosis of group A cell walls than Fisher macrophages. Soluble cytotoxins could not be detected in macrophage culture media.

细菌细胞壁聚合物与大鼠巨噬细胞的相互作用。
用正常大鼠腹膜细胞进行组织培养,测定A组和D组链球菌吞噬后细胞壁的加工情况。与D组相比,A组细胞壁几乎不可生物降解,培养4-8天降解率超过80%。A组细胞壁黏肽或多糖的消除或降解无差异。抗血清和致敏淋巴细胞均不影响持久性。Fisher大鼠(易患A组细胞壁诱导的多发性关节炎)巨噬细胞在摄入A组细胞壁6-7天后对靶l细胞具有细胞毒性。D组细胞壁吞噬作用诱导的细胞毒性较小。水牛大鼠(抗多发性关节炎)巨噬细胞吞噬A组细胞壁后的细胞毒性低于Fisher巨噬细胞。巨噬细胞培养液中未检出可溶性细胞毒素。
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