SPNS2 exports sphingosine-1-phosphate and imports glucose

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Authors: Cynthia Weigel, Md Lokman Hossen, Ryan D. R. Brown, Can E. Senkal, Christopher D. Green, Jason Newton, Sumit Saha, Elisa N.D. Palladino, Bin Ni, Francesco Saverio Celi, Xianjun Fang, Frank D. Corwin
+4 more Huanyu Z. Li, David Bryant Sauer, Prem P. Chapagain, Sarah Spiegel
Cited by: 1
References: 81

Abstract

Spinster homolog 2 (SPNS2) exports the bioactive sphingolipid metabolite sphingosine-1-phosphate (S1P) out of cells to regulate processes important for health and diseases. However, the molecular mechanism underlying SPNS2 transport functions and its precise physiological roles are not fully understood. Here, through a series of complementary approaches in mice, cellular assays, and particularly with in vitro cell-free binding and transport assays, we show that SPNS2 has antiporter-like activity, transporting S1P out of cells and glucose in. We demonstrate that SPNS2 directly binds glucose and transports it and identify key amino acid residues of SPNS2 involved in glucose engagement and import. Our data reveal that S1P, which enters from the cytosolic side of SPNS2 facilitates conformational changes, enabling extracellular glucose to move inward through the central cavity. Thus, we identify a mechanism that dynamically contributes to glucose homeostasis in response to metabolic and sphingolipid cues with clinical and pathophysiological implications. Spinster homolog 2 (SPNS2) exports sphingosine-1- 26 phosphate (S1P) out of cells. Here, the authors show that SPNS2 has antiporter-like activity, exporting S1P while importing glucose, revealing a mechanism linking SPNS2 to glucose homeostasis with clinical implications.

Fields of Study & Subjects

Sphingolipid Metabolism and Signaling Erythrocyte Function and Pathophysiology Caveolin-1 and cellular processes

Publication details

Journal / source
Nature Communications
Publisher
Springer Science and Business Media LLC
Volume
17
Issue
1
Publication date
20 April 2026
Language
EN