Sjödin L, Viitanen E, Gylfe E
Pharmacological Division, Medical Products Agency, Uppsala, Sweden.
J Physiol. 1994 Apr 1;476(1):69-77.
Binding of 125I-labelled peptides, cytoplasmic Ca2+ concentration ([Ca2+]i) and amylase release were studied in guinea-pig pancreatic acinar cells during exposure to substance P (SP), and cholecystokinin octapeptide (CCK-8). Pre-incubation of cells at 22 degrees C with 0.03 nM to 1 microM SP for 10 min or at 37 degrees C for 5 min followed by acid or neutral washes reduced subsequent binding of 125I-Bolton-Hunter reagent-labelled SP (125I-BH-SP) in a biphasic manner by up to 95%. Incubation at 4 degrees C eliminated high-affinity binding of 125I-BH-SP and concentrations of SP above 1 nM were required for inhibition of subsequent tracer binding. Pre-incubation of cells at 37 degrees C with 1 nM to 1 microM CCK-8 for 10 min followed by neutral washes reduced subsequent binding of 125I-BH-CCK-8 by up to 65%. In cell suspensions, the [Ca2+]i response to SP was gradually reduced by pre-exposure to increasing agonist concentrations from 0.2 to 20 nM. Pre-incubation with high SP concentrations for 10 min caused profound reduction of subsequent amylase responses to SP, whereas secretion was little affected in corresponding experiments with CCK-8. Down-regulation of receptor binding is not important during short exposure to CCK-8, but it is a pronounced and rapid phenomenon during SP exposure, which explains tachyphylaxis of [Ca2+]i and amylase responses.
在豚鼠胰腺腺泡细胞暴露于P物质(SP)和八肽胆囊收缩素(CCK - 8)的过程中,研究了125I标记肽的结合、细胞质钙离子浓度([Ca2+]i)和淀粉酶释放。细胞在22℃下用0.03 nM至1 μM的SP预孵育10分钟或在37℃下预孵育5分钟,随后进行酸洗或中性洗涤,可使随后125I - 博尔顿 - 亨特试剂标记的SP(125I - BH - SP)的结合以双相方式减少高达95%。在4℃下孵育可消除125I - BH - SP的高亲和力结合,并且需要高于1 nM的SP浓度来抑制随后的示踪剂结合。细胞在37℃下用1 nM至1 μM的CCK - 8预孵育10分钟,随后进行中性洗涤,可使随后125I - BH - CCK - 8的结合减少高达65%。在细胞悬液中,通过预先暴露于从0.2 nM至20 nM逐渐增加的激动剂浓度,对SP的[Ca2+]i反应逐渐降低。用高浓度SP预孵育10分钟会导致随后对SP的淀粉酶反应大幅降低,而在相应的CCK - 8实验中分泌几乎不受影响。在短时间暴露于CCK - 8期间,受体结合的下调并不重要,但在暴露于SP期间这是一个明显且快速的现象,这解释了[Ca2+]i和淀粉酶反应的快速耐受性。