de Paulis A, Minopoli G, Arbustini E, de Crescenzo G, Dal Piaz F, Pucci P, Russo T, Marone G
Division of Clinical Immunology and Allergy, Department of Biochemistry and Medical Biotechnology, University of Naples Federico II, Italy.
J Immunol. 1999 Sep 1;163(5):2799-808.
Stem cell factor (SCF) is the most important cytokine regulating human mast cell growth and functions. The immunogold technique showed SCF in the secretory granules of skin mast cells and in lung parenchymal mast cells (HLMC). Immunoreactive SCF (iSCF) was detected in cell lysates of HLMC, but not in basophils; iSCF and histamine were detected in supernatants of HLMC 3 min after challenge with anti-FcepsilonRI or anti-IgE, and iSCF in supernatants rapidly declined after 30 min, whereas histamine remained unchanged for 120 min. HPLC and electrospray mass spectrometry (ES/MS) analysis of recombinant human SCF1-166 (18,656. 9 +/- 0.9 Da) treated with chymase showed a polypeptide of 17,977.1 +/- 0.6 Da and a minor component of 697.4 +/- 0.1 Da generated by specific cleavage at Phe159. SCF1-166 and SCF1-159 similarly activated HLMC, potentiated anti-IgE-induced activation of these cells, and stimulated HLMC chemotaxis. SCF159-166 had no effect on mast cells. Western blot analysis of supernatants of anti-IgE-activated HLMC incubated with recombinant human SCF1-166 showed that SCF1-166 was rapidly cleaved to SCF1-159 and SCF1-144. Experiments with supernatants of anti-IgE-activated HLMC incubated with SCF1-166 yielded similar results. In conclusion, SCF is stored in mast cell secretory granules and is immunologically released by human mast cells. SCF1-166 is rapidly and specifically cleaved to SCF1-159 by chymase, which retains its biological effect on mast cells. SCF is also cleaved by other proteases to several SCF species whose possible biological activities remain to be established.
干细胞因子(SCF)是调节人类肥大细胞生长和功能的最重要细胞因子。免疫金技术显示,皮肤肥大细胞和肺实质肥大细胞(HLMC)的分泌颗粒中有SCF。在HLMC的细胞裂解物中检测到免疫反应性SCF(iSCF),但在嗜碱性粒细胞中未检测到;用抗FcepsilonRI或抗IgE刺激3分钟后,在HLMC的上清液中检测到iSCF和组胺,30分钟后上清液中的iSCF迅速下降,而组胺在120分钟内保持不变。用糜蛋白酶处理重组人SCF1-166(18,656.9±0.9 Da)的高效液相色谱(HPLC)和电喷雾质谱(ES/MS)分析显示,产生了17,977.1±0.6 Da的多肽和在Phe159处特异性切割产生的697.4±0.1 Da的次要成分。SCF1-166和SCF1-159同样激活HLMC,增强抗IgE诱导的这些细胞的激活,并刺激HLMC趋化性。SCF159-166对肥大细胞无作用。用重组人SCF1-166孵育抗IgE激活的HLMC的上清液进行蛋白质印迹分析显示,SCF1-166迅速裂解为SCF1-159和SCF1-144。用SCF1-166孵育抗IgE激活的HLMC的上清液进行的实验得出了类似结果。总之,SCF储存在肥大细胞分泌颗粒中,并由人类肥大细胞免疫释放。SCF1-166被糜蛋白酶迅速特异性切割为SCF1-159,后者对肥大细胞保留其生物学效应。SCF也被其他蛋白酶切割为几种SCF种类,其可能的生物学活性仍有待确定。