Proteases Revisited: Roles and Therapeutic Implications in Fibrosis

Joint Authors

Kryczka, Jakub
Boncela, Joanna

Source

Mediators of Inflammation

Issue

Vol. 2017, Issue 2017 (31 Dec. 2017), pp.1-14, 14 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2017-05-31

Country of Publication

Egypt

No. of Pages

14

Main Subjects

Diseases

Abstract EN

Proteases target many substrates, triggering changes in distinct biological processes correlated with cell migration, EMT/EndMT and fibrosis.

Extracellular protease activity, demonstrated by secreted and membrane-bound protease forms, leads to ECM degradation, activation of other proteases (i.e., proteolysis of nonactive zymogens), decomposition of cell-cell junctions, release of sequestered growth factors (TGF-β and VEGF), activation of signal proteins and receptors, degradation of inflammatory inhibitors or inflammation-related proteins, and changes in cell mechanosensing and motility.

Intracellular proteases, mainly caspases and cathepsins, modulate lysosome activity and signal transduction pathways.

Herein, we discuss the current knowledge on the multidimensional impact of proteases on the development of fibrosis.

American Psychological Association (APA)

Kryczka, Jakub& Boncela, Joanna. 2017. Proteases Revisited: Roles and Therapeutic Implications in Fibrosis. Mediators of Inflammation،Vol. 2017, no. 2017, pp.1-14.
https://search.emarefa.net/detail/BIM-1188169

Modern Language Association (MLA)

Kryczka, Jakub& Boncela, Joanna. Proteases Revisited: Roles and Therapeutic Implications in Fibrosis. Mediators of Inflammation No. 2017 (2017), pp.1-14.
https://search.emarefa.net/detail/BIM-1188169

American Medical Association (AMA)

Kryczka, Jakub& Boncela, Joanna. Proteases Revisited: Roles and Therapeutic Implications in Fibrosis. Mediators of Inflammation. 2017. Vol. 2017, no. 2017, pp.1-14.
https://search.emarefa.net/detail/BIM-1188169

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1188169