Format

Send to

Choose Destination
Bone. 2019 Oct 21;130:115087. doi: 10.1016/j.bone.2019.115087. [Epub ahead of print]

The role of sphingosine 1-phosphate metabolism in bone and joint pathologies and ectopic calcification.

Author information

1
Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5246, ICBMS, F-69622, Lyon, France.
2
Institut de Pharmacologie et de Biologie Structurale, IPBS, CNRS UMR 5089, F-31077, Toulouse, France.
3
Univ Lyon, Université Claude Bernard Lyon 1, CNRS UMR 5246, ICBMS, F-69622, Lyon, France. Electronic address: leyre.brizuela-madrid@univ-lyon1.fr.

Abstract

Sphingolipids display important functions in various pathologies such as cancer, obesity, diabetes, cardiovascular or neurodegenerative diseases. Sphingosine, sphingosine 1-phosphate (S1P), and ceramide are the central molecules of sphingolipid metabolism. Sphingosine kinases 1 and 2 (SK1 and SK2) catalyze the conversion of the sphingolipid metabolite sphingosine into S1P. The balance between the levels of S1P and its metabolic precursors ceramide and sphingosine has been considered as a switch that could determine whether a cell proliferates or dies. This balance, also called « sphingolipid rheostat », is mainly under the control of SKs. Several studies have recently pointed out the contribution of SK/S1P metabolic pathway in skeletal development, mineralization and bone homeostasis. Indeed, SK/S1P metabolism participates in different diseases including rheumatoid arthritis, spondyloarthritis, osteoarthritis, osteoporosis, cancer-derived bone metastasis or calcification disorders as vascular calcification. In this review, we will summarize the most important data regarding the implication of SK/S1P axis in bone and joint diseases and ectopic calcification, and discuss the therapeutic potential of targeting SK/S1P metabolism for the treatment of these pathologies.

KEYWORDS:

Arthritis; Osteoporosis; Sphingosine 1-phosphate; Sphingosine kinases; Spondyloarthritis

PMID:
31648078
DOI:
10.1016/j.bone.2019.115087

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center