Ninomiya H, Muraki Y, Shibuya K, Nagasawa T, Abe T
Division of Haematology, University of Tsukuba, Ibaraki, Japan.
Br J Haematol. 1993 Jul;84(3):497-503. doi: 10.1111/j.1365-2141.1993.tb03107.x.
The inducibility of glycosyl-phosphatidylinositol (GPI)-anchored proteins on affected paroxysmal nocturnal haemoglobinuria (PNH) neutrophils (PMN) after both in vitro and in vivo stimulation was investigated. Fc gamma R-III (CD16), decay-accelerating factor (DAF/CD55) and 20 kD homologous restriction factor (HRF20/CD59) were demonstrated to be concurrently deficient on unstimulated defective PNH PMN. Upon in vitro stimulation with either N-formyl-methionyl-leucyl-phenylalanine (fMLP), zymosan-activated serum (ZAS), or recombinant human granulocyte colony-stimulation factor (G-CSF), neither CD16 nor CD55 expression was induced on defective PNH PMN. G-CSF was administered to two patients with PNH when their conditions were complicated by bacterial infections, or to prevent infections associated with the extraction of teeth or cataract surgery. CD16 expression was induced on the defective PNH PMN in both cases during the administration of G-CSF, but the expression of CD55 and CD59 was not. CD16, induced on the defective PNH PMN during the administration of G-CSF, was phosphatidylinositol-specific phospholipase C (PIPLC)-sensitive, implying that it had GPI-linkage to the membranes. The patients treated with G-CSF recovered from infection or evaded infection. These observations suggest that a deficiency of GPI-anchored proteins is not always seen in defective PNH blood cells, at least under certain stimulation conditions.
研究了体外和体内刺激后,受影响的阵发性夜间血红蛋白尿(PNH)中性粒细胞(PMN)上糖基磷脂酰肌醇(GPI)锚定蛋白的诱导性。FcγR-III(CD16)、衰变加速因子(DAF/CD55)和20kD同源限制因子(HRF20/CD59)在未刺激的缺陷型PNH PMN上被证明同时缺乏。在用N-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)、酵母聚糖激活血清(ZAS)或重组人粒细胞集落刺激因子(G-CSF)进行体外刺激后,缺陷型PNH PMN上既未诱导CD16也未诱导CD55表达。当两名PNH患者病情因细菌感染而复杂化,或为预防与拔牙或白内障手术相关的感染时,给予他们G-CSF。在给予G-CSF期间,两例患者的缺陷型PNH PMN上均诱导出CD16表达,但CD55和CD59未表达。在给予G-CSF期间,缺陷型PNH PMN上诱导出的CD16对磷脂酰肌醇特异性磷脂酶C(PIPLC)敏感,这意味着它与膜有GPI连接。接受G-CSF治疗的患者感染痊愈或避免了感染。这些观察结果表明,至少在某些刺激条件下,GPI锚定蛋白的缺乏在缺陷型PNH血细胞中并不总是可见的。