Kimball H R, Ford G H, Wolff S M
J Lab Clin Med. 1975 Oct;86(4):616-30.
A method of blood granylocyte concentration and isolation of granules from both normal and neutropenic Chediak-Higashi syndrome (CHS) patients is described. the intracellular distribution of activity for several hydrolases in CHS granulocytes differs from normal; significantly more activity is present in the cytoplasmic fraction and correspondingly less is granule-associated. Isolated CHS granules are not more sensitive to the labilizing agents vitamin A, progesterone, or etiocholanolone. Specific activities of myeloperoxidase and ss-glucuronidase in CHS granulocytes are lower than normal while alkaline phosphatase is elevated. Other lysosomal enzyme activities are normal. Lysosomal enzyme distribution and content are similar in CHS and normal mononuclear cells. The possible significance of these findings is discussed.
描述了一种用于测定正常和嗜中性粒细胞减少的切-东综合征(CHS)患者血液粒细胞浓度以及从其中分离颗粒的方法。CHS粒细胞中几种水解酶的细胞内活性分布与正常情况不同;细胞质部分中的活性明显更多,而与颗粒相关的活性相应更少。分离出的CHS颗粒对不稳定剂维生素A、孕酮或本胆烷醇酮并不更敏感。CHS粒细胞中髓过氧化物酶和β-葡萄糖醛酸酶的比活性低于正常水平,而碱性磷酸酶则升高。其他溶酶体酶活性正常。CHS和正常单核细胞中的溶酶体酶分布和含量相似。讨论了这些发现的可能意义。