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The Role of TAM Family Receptors and Ligands in the Nervous System: From Development to Pathobiology
- Publication Year :
- 2018
-
Abstract
- Tyro3, Axl, and Mertk, referred to as the TAM family of receptor tyrosine kinases, are instrumental in maintaining cell survival and homeostasis in mammals. TAM receptors interact with multiple signaling molecules to regulate cell migration, survival, phagocytosis and clearance of metabolic products and cell debris called efferocytosis. The TAMs also function as rheostats to reduce the expression of proinflammatory molecules and prevent autoimmunity. All three TAM receptors are activated in a concentration-dependent manner by the vitamin K–dependent growth arrest-specific protein 6 (Gas6). Gas6 and the TAMs are abundantly expressed in the nervous system. Gas6, secreted by neurons and endothelial cells, is the sole ligand for Axl. ProteinS1 (ProS1), another vitamin K–dependent protein functions mainly as an anti-coagulant, and independent of this function can activate Tyro3 and Mertk, but not Axl. This review will focus on the role of the TAM receptors and their ligands in the nervous system. We highlight studies that explore the function of TAM signaling in myelination, the visual cortex, neural cancers, and multiple sclerosis (MS) using Gas6−/− and TAM mutant mice models.
- Subjects :
- 0301 basic medicine
Cell signaling
Multiple Sclerosis
Vitamin K
Biology
Ligands
Nervous System
Receptor tyrosine kinase
Article
Proinflammatory cytokine
Protein S
03 medical and health sciences
Mice
stomatognathic system
Proto-Oncogene Proteins
Animals
Humans
Pharmacology (medical)
Receptor
Efferocytosis
skin and connective tissue diseases
Pharmacology
c-Mer Tyrosine Kinase
GAS6
Receptor Protein-Tyrosine Kinases
Blood Proteins
MERTK
Axl Receptor Tyrosine Kinase
Cell biology
030104 developmental biology
biology.protein
Intercellular Signaling Peptides and Proteins
hormones, hormone substitutes, and hormone antagonists
TYRO3
Signal Transduction
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....4a4d5ab4e926140526b76afb067da2ae