Baggiolini M, Schnyder J, Dewald B, Bretz U, Payne T G
Immunobiology. 1982 Apr;161(3-4):369-75. doi: 10.1016/S0171-2985(82)80094-6.
Quiescent mouse peritoneal macrophages which phagocytose, and which respond to phagocytosis with a sudden elevation in hexose monophosphate shunt activity, immediately release into the medium oxygen metabolites, arachidonic acid oxygenation products, and lysosomal hydrolases. Such cells subsequently differentiate and acquire the properties of inflammatory macrophages. The latter process appears to be under the control of prostaglandin E2 and possibly other cyclooxygenase products which are formed as a consequence of phagocytosis and seem to act as feed-back inhibitors.
静止的小鼠腹膜巨噬细胞具有吞噬作用,并且在吞噬后会因磷酸己糖支路活性突然升高而做出反应,它们会立即将氧代谢产物、花生四烯酸氧化产物和溶酶体水解酶释放到培养基中。这些细胞随后会分化并获得炎性巨噬细胞的特性。后一过程似乎受前列腺素E2以及可能其他因吞噬作用而形成的环氧化酶产物的控制,这些产物似乎起到反馈抑制剂的作用。