{"created":"2020-08-30T20:01:39.383010+00:00","id":3140,"links":{},"metadata":{"_buckets":{"deposit":"16b78398-01d9-430d-9f8f-2a3d29483ac5"},"_deposit":{"id":"3140","owners":[],"pid":{"revision_id":0,"type":"recid","value":"3140"},"status":"published"},"_oai":{"id":"oai:meral.edu.mm:recid/3140","sets":["1582963366982:1596631591423"]},"communities":["um1"],"item_1583103067471":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_1551255647225":"Catestatin, a neuroendocrine antimicrobial peptide, induces human mast cell migration, degranulation and production of cytokines and chemokines","subitem_1551255648112":""}]},"item_1583103085720":{"attribute_name":"Description","attribute_value_mlt":[{"interim":"

Catestatin, a neuroendocrine peptide with effects on human autonomic function, has recently been found to be a cutaneous antimicrobial peptide. Human catestatin exhibits three single nucleotide polymorphisms: Gly364- Ser, Pro370Leu and Arg374Gln. Given reports indicating that antimicrobial peptides and neuropeptides induce mast cell activation, we postulated that catestatin might stimulate numerous functions of human mast cells, thereby participating in the regulation of skin inflammatory responses. Catestatin and its naturally occurring variants caused the human mast cell line LAD2 and peripheral blood-derived mast cells to migrate, degranulate and release leukotriene C4 and prostaglandins D2 and E2. Moreover, catestatins increased intracellular Ca2+ mobilization in mast cells, and induced the production of pro-inflammatory cytokines/chemokines such as granulocyte–macrophage colony-stimulating factor, monocyte chemotactic protein-1/CCL2, macrophage inflammatory protein-1a/CCL3 and
\nmacrophage inflammatory protein-1b/CCL4.

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