Related Experiment Video
Updated: Sep 19, 2025

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
Immunomodulatory properties of transmembrane mucins: from chronic diseases to cancer
Paula Montero1,2,3, Inés Roger1,2,3, Javier Milara1,3,4
1Department of Pharmacology, Faculty of Medicine, University of Valencia, Valencia, Spain.
Mucins are large glycoproteins that form the primary structural component of mucus and can be classified into secreted and transmembrane types. Of the 22 identified mucin genes, 12 encode transmembrane mucins, which play crucial roles in maintaining epithelial barrier integrity, modulating cell signaling, and innate immune responses to pathogens. Transmembrane mucins are expressed in epithelial cells, inflammatory cells, endothelial cells, and fibroblasts, influencing diverse cellular processes. They interact with extracellular ligands and transduce intracellular signals, functioning as membrane receptors with cell type-specific effects, triggering anti-inflammatory, proliferative, fibrotic, or carcinogenic processes. The extracellular domain of mucins can also be shed into the environment, where it exerts biological functions and serves as a biomarker for various chronic diseases. This review presents a comprehensive analysis of the discovery, structure, and molecular composition of different transmembrane mucins, along with their expression patterns and distribution across tissues. It explores their physiological roles and immunomodulatory functions and the diverse cellular processes they regulate. Furthermore, it discusses the contribution of transmembrane mucin gene variants, aberrant expression, and dysregulated activation in chronic diseases such as inflammation, fibrosis, and cancer. Finally, given the role of mucins in the progression of various pathologies, this review describes therapeutic strategies and biomarkers that have been translated into clinical practice with promising results, aiming to provide a comprehensive overview of the current understanding of transmembrane mucins.
Mucins are large glycoproteins that form the primary structural component of mucus and can be classified into secreted and transmembrane types. Of the 22 identified mucin genes, 12 encode transmembrane mucins, which play crucial roles in maintaining epithelial barrier integrity, modulating cell signaling, and innate immune responses to pathogens. Transmembrane mucins are expressed in epithelial cells, inflammatory cells, endothelial cells, and fibroblasts, influencing diverse cellular processes. They interact with extracellular ligands and transduce intracellular signals, functioning as membrane receptors with cell type-specific effects, triggering anti-inflammatory, proliferative, fibrotic, or carcinogenic processes. The extracellular domain of mucins can also be shed into the environment, where it exerts biological functions and serves as a biomarker for various chronic diseases. This review presents a comprehensive analysis of the discovery, structure, and molecular composition of different transmembrane mucins, along with their expression patterns and distribution across tissues. It explores their physiological roles and immunomodulatory functions and the diverse cellular processes they regulate. Furthermore, it discusses the contribution of transmembrane mucin gene variants, aberrant expression, and dysregulated activation in chronic diseases such as inflammation, fibrosis, and cancer. Finally, given the role of mucins in the progression of various pathologies, this review describes therapeutic strategies and biomarkers that have been translated into clinical practice with promising results, aiming to provide a comprehensive overview of the current understanding of transmembrane mucins.
More Related Videos
09:24Mucin Agarose Gel Electrophoresis: Western Blotting for High-molecular-weight Glycoproteins
Published on: June 14, 2016
07:05Important Endpoints and Proliferative Markers to Assess Small Intestinal Injury and Adaptation using a Mouse Model of Chemotherapy-Induced Mucositis
Published on: May 12, 2019
Related Concept Videos
The Tumor Microenvironment
Mitogens and the Cell Cycle
Cell-mediated Immune Responses
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...