Middelhoven P J, Ager A, Roos D, Verhoeven A J
Central Laboratory of the Netherlands Red Cross Blood Transfusion Service, and University of Amsterdam, The Netherlands.
FEBS Lett. 1997 Sep 1;414(1):14-8. doi: 10.1016/s0014-5793(97)00959-9.
Fc gammaRIIIb is a glycosylphosphatidylinositol(GPI)-anchored, low-affinity IgG receptor, expressed exclusively on human neutrophils. Upon activation or apoptosis of neutrophils, Fc gammaRIIIb is shed from the cell surface, but the enzyme(s) responsible for this process is (are) still unknown. Recently, metalloproteases have been suggested to mediate the shedding of cell surface proteins such as L-selectin and TNF-alpha. Using hydroxamic acid-based inhibitors of this class of proteases (BB-3103, Ro31-9790), we have observed a clear inhibitory effect on Fc gammaRIIIb shedding after PMA stimulation of neutrophils or induction of apoptosis. These inhibitors did not affect PMA-induced degranulation or superoxide generation.
FcγRIIIb是一种糖基磷脂酰肌醇(GPI)锚定的低亲和力IgG受体,仅在人类中性粒细胞上表达。当中性粒细胞激活或凋亡时,FcγRIIIb从细胞表面脱落,但负责此过程的酶仍不清楚。最近,有人提出金属蛋白酶介导细胞表面蛋白如L-选择素和TNF-α的脱落。使用基于异羟肟酸的这类蛋白酶抑制剂(BB-3103、Ro31-9790),我们观察到在PMA刺激中性粒细胞或诱导凋亡后,对FcγRIIIb脱落有明显的抑制作用。这些抑制剂不影响PMA诱导的脱颗粒或超氧化物生成。