Crivellato E, Candussio L, Decorti G, Klugmann F B, Mallardi F
Department of Medical and Morphological Research, University of Udine, Italy.
J Submicrosc Cytol Pathol. 1999 Apr;31(2):279-86.
The process of exocytosis was studied in rat and beige mouse peritoneal mast cells stimulated by adriamycin (ADR) at 37 degrees C and 22 degrees C. ADR induces a non cytotoxic histamine release that is followed by a significant uptake of the drug. Examination was performed by transmission electron microscopy and, at the same time, histamine release and ADR uptake were measured by spectrofluorimetry. ADR accumulation in mast cells was investigated also by fluorescence microscopy. In rat mast cells stimulated at 37 degrees C, the secretory process developed abruptly and was virtually complete after 30 sec. Electron microscopy showed rapid intracytoplasmic channel formation and extrusion of secretory granules; spectrofluorimetry revealed a massive release of histamine and rapid uptake of ADR. In addition, fluorescence microscopy showed mast cells exhibiting an intense orange-yellow fluorescent signal localized at the secretory granules. At 22 degrees C, rat mast cells showed alteration of the granules, cavity formation by fusion of the perigranular membrane and granule discharge due to fusion of the cavity membrane with the cell membrane. Histamine release and ADR uptake proceeded less quickly than at 37 degrees C. Quantitative analysis of rat mast cell ultrastructure demonstrated that histamine release induced by ADR stimulation was achieved by sequential exocytosis. This process presents both morphological and biochemical affinities with the exocytosis induced by basic secretagogues such as compound 48/80. In beige mouse mast cells the process of exocytosis progressed more slowly and was completed after 20 min at 37 degrees C. By electron microscopy, the cytoplasm presented a rigid structure due to abundance of actin-like fibrils. Granule fusion was an uncommon feature and exocytosis was mostly the result of single granule opening to the cell exterior without extrusion of granule matrices.
在37℃和22℃条件下,研究了阿霉素(ADR)刺激大鼠和米色小鼠腹膜肥大细胞时的胞吐过程。ADR诱导非细胞毒性的组胺释放,随后药物大量摄取。通过透射电子显微镜进行检查,同时用荧光分光光度法测量组胺释放和ADR摄取。还通过荧光显微镜研究了肥大细胞中ADR的积累情况。在37℃刺激的大鼠肥大细胞中,分泌过程突然开始,30秒后基本完成。电子显微镜显示胞浆内迅速形成通道,分泌颗粒排出;荧光分光光度法显示组胺大量释放,ADR迅速摄取。此外,荧光显微镜显示肥大细胞的分泌颗粒处呈现强烈的橙黄色荧光信号。在22℃时,大鼠肥大细胞显示颗粒改变,颗粒周围膜融合形成腔,腔膜与细胞膜融合导致颗粒排出。组胺释放和ADR摄取比在37℃时进行得慢。对大鼠肥大细胞超微结构的定量分析表明,ADR刺激诱导的组胺释放是通过连续胞吐实现的。这个过程在形态学和生物化学上与碱性促分泌剂如化合物48/80诱导的胞吐作用有相似之处。在米色小鼠肥大细胞中,胞吐过程进展较慢,在37℃时20分钟后完成。通过电子显微镜观察,由于肌动蛋白样纤维丰富,细胞质呈现刚性结构。颗粒融合不常见,胞吐主要是单个颗粒向细胞外开放而不挤出颗粒基质的结果。