THE ROLE OF MUCINS AND MUCUS IN THE DISEASES CYSTIC FIBROSIS CELIAC DISEASE AN...
THE ROLE OF MUCINS AND MUCUS IN THE DISEASES CYSTIC FIBROSIS CELIAC DISEASE AND ULCERATIVE COLITIS
The overall aim of this proposal is to explain how the mucus systems of the intestine and lung act as a first innate immune defense line to protect our mucosal surfaces. Mucins are of highly glycosylated proteins that build the mu...
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Duración del proyecto: 60 meses
Fecha Inicio: 2016-08-05
Fecha Fin: 2021-08-31
Líder del proyecto
GOETEBORGS UNIVERSITET
No se ha especificado una descripción o un objeto social para esta compañía.
TRL
4-5
Presupuesto del proyecto
3M€
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
The overall aim of this proposal is to explain how the mucus systems of the intestine and lung act as a first innate immune defense line to protect our mucosal surfaces. Mucins are of highly glycosylated proteins that build the mucus skeleton.
We previously discovered that there are two mucus layers in the colon. The inner mucus layer built around the MUC2 mucin is attached and impenetrable to bacteria, thus separating the intestinal bacteria from the epithelial cells. However, how the dynamic colon mucus layers are formed and controlled is poorly understood.
We have established an international leading position in this research area and will now address fundamental and unresolved problems of high medical importance. The capacity of the inner mucus layer to separate bacteria from the epithelium is highly dependent on the luminal bacteria. Our results suggest specific bacteria signaling via smaller molecules or bacterial fragments to the host to increase protection. We will reveal how this signaling take place, important for understanding increased western world diseases including ulcerative colitis. Of special interest is our recent finding of a single sensory goblet cell protecting the colon crypts. We have developed a fluorescent human MUC2 transgenic mouse that is instrumental for the planned studies as well as in studies of gliadin uptake from the intestine and initiator for celiac disease.
We will now transfer our leading edge knowledge of intestinal mucus structure and function to the respiratory tract. Normal trachea seems to be cleared by mucus strands formed the tracheal glands, but these strands are trapped cystic fibrosis. We will also reveal how a hypothetic attached mucus layer, as described by us in colon, could explain the mucus accumulation in chronic lung diseases.
The proposed project will substantially increase our basic understanding of molecular mechanisms behind several mucus related diseases and pave the way for new treatments.