TAM receptors, Gas6, and protein S: roles in inflammation and hemostasis.

Abstract

TAM receptors (Tyro3, Axl, and Mer) belong to a family of receptor tyrosine kinases that have important effects on hemostasis and inflammation. Also, they affect cell proliferation, survival, adhesion, and migration. TAM receptors can be activated by the vitamin K-dependent proteins Gas6 and protein S. Protein S is more commonly known as an important cofactor for protein C as well as a direct inhibitor of multiple coagulation factors. To our knowledge, the functions of Gas6 are limited to TAM receptor activation. When activated, the TAM receptors have effects on primary hemostasis and coagulation and display an anti-inflammatory or a proinflammatory effect, depending on cell type. To comprehend the effects that the TAM receptors and their ligands have on hemostasis and inflammation, we compare studies that report the different phenotypes displayed by mice with deficiencies in the genes of this receptor family and its ligands (protein S(+/-), Gas6(-/-), TAM(-/-), and variations of these). In this manner, we aim to display which features are attributable to the different ligands. Because of the effects TAM receptors have on hemostasis, inflammation, and cancer growth, their modulation could make interesting therapeutic targets in thromboembolic disease, atherosclerosis, sepsis, autoimmune disease, and cancer.

• Authors: Jonathan H M van der Meer, Tom van der Poll, Cornelis van 't Veer
• Journal: Blood (Blood) Vol. 123 Issue 16 Pg. 2460-9 (Apr 17 2014) ISSN: 1528-0020 [Electronic] United States
• PMID: 24596417 (Publication Type: Journal Article, Review)

Chemical References

• Intercellular Signaling Peptides and Proteins
• Protein S
• Proto-Oncogene Proteins
• growth arrest-specific protein 6
• MERTK protein, human
• Receptor Protein-Tyrosine Kinases
• TYRO3 protein, human
• c-Mer Tyrosine Kinase
• Axl Receptor Tyrosine Kinase

Topics

• Animals
• Hemostasis (genetics)
• Humans
• Inflammation (genetics, metabolism)
• Intercellular Signaling Peptides and Proteins (physiology)
• Mice
• Protein S (physiology)
• Proto-Oncogene Proteins (physiology)
• Receptor Protein-Tyrosine Kinases (physiology)
• c-Mer Tyrosine Kinase
• Axl Receptor Tyrosine Kinase