LIM Kinases: From Molecular to Pathological Features
A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Pathology".
Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 24170
Special Issue Editors
Interests: cell signaling; LIM kinases; neurofibromatosis type I; cytoskeleton remodeling; post-translational modifications (SUMO)
Special Issue Information
Dear Colleagues,
The LIM kinases LIMK1 and LIMK2 were discovered in 1994 and 1995, respectively. They were characterized as dual kinases phosphorylating both Ser/Thr and Tyr residues. Their role in actin cytoskeleton remodeling was quickly demonstrated via the inhibition of their substrate actin depolymerizing factor ADF/cofilin. They also regulate microtubule polymerization, but the molecular actors in this process remain unknown. According to their role in cytoskeleton remodeling, LIM kinases contribute to many cellular functions, such as cell motility, morphogenesis, division, differentiation, apoptosis, neuronal morphology, neuritogenesis, and oncogenesis. Recently, the number of LIM kinase substrates has started to grow, suggesting other functions for these proteins. In the last 10 years, LIM kinases have also attracted special attention as their involvement in several diseases has been shown.
In this Special Issue, we want to provide an extensive overview of these very peculiar kinases, starting from their molecular characterization and ending with their pathological implications. A first set of reviews will describe their three-dimensional structure and their non-conventional interaction with their well-characterized substrate cofilin. A second set of reviews will focus on their different, less-known substrates, on their regulators, and on the different cell signaling pathways they are part of. A third set of reviews will focus on the different diseases in which LIM kinases are involved and for which they constitute emerging therapeutic targets: cancer, neurological diseases, viral infection, and reproduction defects. Finally, a fourth set reviews will update the different strategies for inhibiting these kinases: small chemical molecules, miR.
Dr. Hélène Bénédetti
Dr. Béatrice Vallée-Méheust
Guest Editors
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Keywords
- LIM kinases
- cytoskeleton
- cofilin
- cell signaling pathways
- cancer
- neurological defects
- kinase inhibitors
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