Latimer K S, Crane L S, Prasse K W
Am J Vet Res. 1981 Jul;42(7):1254-6.
A quantitative evaluation of neutrophilic chemotaxis was performed, using neutrophils from 12 healthy Beagles. Dextran sedimentation, differential centrifugation, and hypotonic lysis allowed separation of a neutrophil-rich cell suspension. Chemotaxis was studied, using blind-well chambers with 3-micrometers (APD) polycarbonate filters. A frozen (-80 C) bank of pooled normal canine serum was used as the chemotactant, and the chemotactant properties of the serum were destroyed by heat inactivation at 56 C for 30 minutes. Based on membrane and lower blind-well chamber solution neutrophil counts, a method was devised to distinguish between normal neutrophilic chemotaxis, normal neutrophilic chemotaxis with decreased neutrophilic adherence, and defective neutrophilic chemotaxis.
利用12只健康比格犬的中性粒细胞进行了中性粒细胞趋化性的定量评估。通过葡聚糖沉降、差速离心和低渗裂解来分离富含中性粒细胞的细胞悬液。趋化性研究采用带有3微米孔径(孔径分布偏差)聚碳酸酯滤膜的盲孔小室。使用储存在-80℃的混合正常犬血清库作为趋化剂,血清的趋化剂特性通过在56℃加热灭活30分钟来破坏。基于膜和下部盲孔小室溶液中的中性粒细胞计数,设计了一种方法来区分正常中性粒细胞趋化性、中性粒细胞黏附性降低的正常中性粒细胞趋化性以及缺陷性中性粒细胞趋化性。