Mege J L, Capo C, Michel B, Gastaut J L, Bongrand P
Laboratoire d'Immunologie, Hôpital de Sainte-Marguerite, Marseille, France.
Neurobiol Aging. 1988 Mar-Apr;9(2):217-20. doi: 10.1016/s0197-4580(88)80054-x.
In order to study the activity of phagocytic cells in normal and pathological aging, we compared normal young and aged subjects and patients with Alzheimer's (AD) or Parkinson's (PD) disease. Blood granulocytes and monocytes were separately assayed for ingestion of three different particle species (opsonized zymosan, immunoglobulin-coated sheep red cells (IgG-SRC) and glutaraldehyde-treated sheep red cells (G-SRC]. The superoxide anion production induced by these particles was also measured. All granulocyte responses to zymosan and IgG-SRC were depressed in the three aged groups as compared to young controls. Hence, only functions involving a specific receptor (Fc or C3b receptor) seemed affected. Monocyte activity was slightly decreased in the same groups. No difference was found between AD or PD patients and normal aged subjects. Hence the phagocytic and oxidative defects we found were a consequence of aging.
为了研究正常衰老和病理性衰老过程中吞噬细胞的活性,我们比较了正常年轻受试者、老年受试者以及患有阿尔茨海默病(AD)或帕金森病(PD)的患者。分别检测了血液中的粒细胞和单核细胞对三种不同颗粒物质(调理酵母聚糖、免疫球蛋白包被的绵羊红细胞(IgG-SRC)和戊二醛处理的绵羊红细胞(G-SRC))的摄取情况。还测量了这些颗粒诱导产生的超氧阴离子。与年轻对照组相比,所有三个老年组中粒细胞对酵母聚糖和IgG-SRC的反应均降低。因此,似乎只有涉及特定受体(Fc或C3b受体)的功能受到了影响。同一组中的单核细胞活性略有下降。AD或PD患者与正常老年受试者之间未发现差异。因此,我们发现的吞噬和氧化缺陷是衰老的结果。