Dermatan sulphate is an activating ligand of anaplastic lymphoma kinase

Abstract Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase (RTK) that harbours a tyrosine kinase domain in its intracellular region and is expressed in both central and peripheral nervous systems. RTKs are activated upon ligand binding and receptor clustering; however, ALK remains an or...

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Veröffentlicht in:Journal of biochemistry (Tokyo) 2021-11, Vol.170 (5), p.631-637
Hauptverfasser: Machino, Masaaki, Gong, Yuanhao, Ozaki, Tomoya, Suzuki, Yuji, Watanabe, Eri, Imagama, Shiro, Kadomatsu, Kenji, Sakamoto, Kazuma
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Sprache:eng
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Zusammenfassung:Abstract Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase (RTK) that harbours a tyrosine kinase domain in its intracellular region and is expressed in both central and peripheral nervous systems. RTKs are activated upon ligand binding and receptor clustering; however, ALK remains an orphan receptor despite its pathological significance, especially in malignancy. Recent biochemical work showed that heparan sulphate (HS), an unbranched sulphated glycan, acts as a ligand for and activates ALK. Here, we show that dermatan sulphate (DS, chondroitin sulphate B) directly interacts with the extracellular N-terminal region of ALK as well as HS. The tetrasaccharide of DS was required and was sufficient for inducing autophosphorylation of ALK at tyrosine 1604, a marker for activated ALK. Interestingly, longer oligosaccharides caused enhanced activation of ALK, as was the case for HS. Our results provide a novel example of glycans as signalling molecules and shed light on the pathophysiological roles of ALK. Graphical Abstract Graphical Abstract
ISSN:0021-924X
1756-2651
DOI:10.1093/jb/mvab085