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Mucin-1 is required for Coxsackie Virus B3-induced inflammation in pancreatitis

The Muc-1 oncoprotein is a tumor-associated mucin often overexpressed in pancreatic cancer. We report that knockout of Muc-1 reduced the degree of pancreatic inflammation that resulted from infection with Coxsackievirus B3 (CVB3) in a mouse model. CVB3-infected Muc-1-deficient (Muc-1(KO)) mice had s...

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Detalles Bibliográficos
Autores principales: Liu, Xiang, Clemens, Dahn L., Grunkemeyer, James A., Price, Jeffrey D., O’Connell, Kelly, Chapman, Nora M., Storz, Peter, Wen, Haitao, Cox, Jesse L., Reid, Whitney L., Hollingsworth, Michael A., Thayer, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650496/
https://www.ncbi.nlm.nih.gov/pubmed/31337812
http://dx.doi.org/10.1038/s41598-019-46933-y
Descripción
Sumario:The Muc-1 oncoprotein is a tumor-associated mucin often overexpressed in pancreatic cancer. We report that knockout of Muc-1 reduced the degree of pancreatic inflammation that resulted from infection with Coxsackievirus B3 (CVB3) in a mouse model. CVB3-infected Muc-1-deficient (Muc-1(KO)) mice had significantly reduced infiltration of macrophages into the murine pancreas. We found that Muc-1 signaling through NF-κB increased expression of ICAM-1, a pro-inflammatory mediator that recruits macrophages. Further investigation revealed that bone marrow derived macrophages (BMDM) from the Muc-1(KO) mice exhibited defective migration properties, in part due to low expression of the C-C motif chemokine receptor (CCR2) and the integrin Very Late Antigen 4 (VLA-4). The results presented here provide novel insight into the role of Muc-1 in regulating the inflammatory response and the cellular microenvironment in pancreatitis.