PMID- 13679305 OWN - NLM STAT- MEDLINE DCOM- 20040224 LR - 20200930 IS - 0363-6143 (Print) IS - 0363-6143 (Linking) VI - 286 IP - 2 DP - 2004 Feb TI - IgE alone-induced actin assembly modifies calcium signaling and degranulation in RBL-2H3 mast cells. PG - C256-63 AB - In the mast cell signaling pathways, the binding of immunoglobulin E (IgE) to FcepsilonRI, its high-affinity receptor, is generally thought to be a passive step. In this study, we examined the effect of IgE alone, that is, without antigen stimulation, on the degranulation in mast cells. Monomeric IgE (500-5,000 ng/ml) alone increased cytosolic Ca2+ level ([Ca2+]i) and induced degranulation in rat basophilic leukemia (RBL)-2H3 mast cells. Monomeric IgE (5,000 ng/ml) alone also increased [Ca2+]i and induced degranulation in bone marrow-derived mast cells. Interestingly, monomeric IgE (5-50 ng/ml) alone, in concentrations too low to induce degranulation, increased filamentous actin content in RBL-2H3 mast cells. We next examined whether actin dynamics affect the IgE alone-induced RBL-2H3 mast cell activation pathways. Cytochalasin D inhibited the ability of IgE alone (50 ng/ml) to induce de novo actin assembly. In cytochalasin D-treated cells, IgE (50 ng/ml) alone increased [Ca2+]i and induced degranulation. We have summarized the current findings into two points. First, IgE alone increases [Ca2+]i and induces degranulation in mast cells. Second, IgE, at concentrations too low to increase either [Ca2+]i or degranulation, significantly induces actin assembly, which serves as a negative feedback control in the mast cell Ca2+ signaling and degranulation. FAU - Oka, Tatsuya AU - Oka T AD - Department of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan. FAU - Hori, Masatoshi AU - Hori M FAU - Tanaka, Akane AU - Tanaka A FAU - Matsuda, Hiroshi AU - Matsuda H FAU - Karaki, Hideaki AU - Karaki H FAU - Ozaki, Hiroshi AU - Ozaki H LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20030917 PL - United States TA - Am J Physiol Cell Physiol JT - American journal of physiology. Cell physiology JID - 100901225 RN - 0 (Actins) RN - 37341-29-0 (Immunoglobulin E) RN - SY7Q814VUP (Calcium) SB - IM MH - Actins/*drug effects/metabolism/*physiology MH - Animals MH - Calcium/metabolism MH - Calcium Signaling/*physiology MH - Cell Degranulation/drug effects/*physiology MH - Cell Line, Tumor MH - Immunoglobulin E/*pharmacology MH - Intracellular Membranes/metabolism MH - Mast Cells/drug effects/*physiology MH - Osmolar Concentration MH - Rats EDAT- 2003/09/19 05:00 MHDA- 2004/02/26 05:00 CRDT- 2003/09/19 05:00 PHST- 2003/09/19 05:00 [pubmed] PHST- 2004/02/26 05:00 [medline] PHST- 2003/09/19 05:00 [entrez] AID - 00197.2003 [pii] AID - 10.1152/ajpcell.00197.2003 [doi] PST - ppublish SO - Am J Physiol Cell Physiol. 2004 Feb;286(2):C256-63. doi: 10.1152/ajpcell.00197.2003. Epub 2003 Sep 17.