Signalling and functional diversity within the Axl subfamily of receptor tyrosine kinases
Sassan Hafizi1, Björn Dahlbäck
1Department of Clinical Chemistry, Lund University, Wallenberg Laboratory, University Hospital Malmö, SE-205 02 Malmö, Sweden. sassan.hafizi@med.lu.se
Abstract:
The related Axl, Sky and Mer receptor tyrosine kinases (RTKs) are increasingly being implicated in a host of discrete cellular responses including cell survival, proliferation, migration and phagocytosis. Furthermore, their ligands Gas6 and protein S are characteristically dependent on vitamin K for expression of their functions. The Gas6/Axl system is implicated in several types of human cancer as well as inflammatory, autoimmune, vascular and kidney diseases. Each member of the Axl RTK subfamily possesses distinct expression profiles as well as discrete functions. In this article, we review the knowledge so far on the intracellular signalling interactions and pathways concerning each of the Axl RTKs. In this way, we hope to gain a greater understanding of the mechanisms that set each of them apart, and that relay their associated functions.
Insights
This review explores Axl receptor tyrosine kinases (RTKs), their ligands, and their roles in cell functions and diseases. Understanding their distinct signaling pathways is key to deciphering their specific cellular roles and associated functions.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Axl, Sky, and Mer receptor tyrosine kinases (RTKs) regulate critical cellular processes like survival, proliferation, migration, and phagocytosis.
- Their ligands, Gas6 and protein S, require vitamin K for functional expression.
- The Gas6/Axl system is linked to human cancers and inflammatory, autoimmune, vascular, and kidney diseases.
Purpose of the Study:
- To review intracellular signaling interactions and pathways of Axl RTK subfamily members.
- To elucidate the distinct mechanisms differentiating each Axl RTK.
- To understand how these RTKs relay their associated functions.
Main Methods:
- Literature review of existing research on Axl, Sky, and Mer RTKs.
- Analysis of intracellular signaling pathways and interactions.
- Comparison of expression profiles and functions across the Axl RTK subfamily.
Main Results:
- Each Axl RTK subfamily member exhibits unique expression patterns.
- Distinct cellular functions are associated with each specific RTK.
- Intracellular signaling pathways vary among Axl, Sky, and Mer RTKs.
Conclusions:
- Detailed understanding of individual Axl RTK signaling mechanisms is crucial.
- Elucidating these pathways can provide insights into disease mechanisms.
- This knowledge may facilitate the development of targeted therapies for related diseases.
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