Johnson D, Seeldrayers P A, Weiner H L
Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115.
Brain Res. 1988 Mar 15;444(1):195-8. doi: 10.1016/0006-8993(88)90929-8.
Incubation of bovine peripheral myelin with supernatants from degranulated rat serosal mast cells led to extensive loss of P0. Similarly, when myelinated axons prepared from guinea pig CNS were incubated with degranulation supernatants, a significant loss of basic protein (MBP) was observed. As cationic peptides can stimulate mast cell degranulation, rat serosal mast cells were incubated with MBP, and with P2. Degranulation was assayed by measurement of release of the granule enzyme beta-hexosaminidase and it was found that both MBP and P2 stimulated 40-50% degranulation at a concentration of 50 micrograms/ml. The results of this study suggest that release of mast cell proteases could contribute to myelin damage in both the PNS and CNS, and that subsequent release of P2 or MBP or their breakdown products could potentiate further mast cell degranulation.
将牛周围神经髓磷脂与脱颗粒大鼠浆膜肥大细胞的上清液一起孵育,导致P0大量损失。同样,当用豚鼠中枢神经系统制备的有髓轴突与脱颗粒上清液一起孵育时,观察到碱性蛋白(MBP)显著损失。由于阳离子肽可刺激肥大细胞脱颗粒,将大鼠浆膜肥大细胞与MBP和P2一起孵育。通过测量颗粒酶β-己糖胺酶的释放来检测脱颗粒情况,结果发现,在浓度为50微克/毫升时,MBP和P2均刺激40 - 50%的脱颗粒。本研究结果表明,肥大细胞蛋白酶的释放可能导致外周神经系统和中枢神经系统中的髓磷脂损伤,并且随后P2或MBP或其分解产物的释放可能会增强肥大细胞的进一步脱颗粒。