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May 7, 2026BMC Biology0 citationsOpen Access

TRAM-LAG1-CLN8 domain-containing protein TMEM56 regulates cell migration by changing intracellular ceramide levels

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BDBenjamin DorschnerRWRalf WiedemuthCRCornelia Richter

Key Points

  • To explore the role of TMEM56 in regulating cell migration and its molecular mechanisms.
  • shRNA screen to identify TMEM56
  • lipidomic analysis to assess ceramide levels
  • co-immunoprecipitation to study TMEM56 interactions
  • TMEM56 modulates ceramide metabolism, particularly hexosylated ceramides
  • TMEM56 interacts with ceramide synthase 2
  • TMEM56 is crucial for SDF-1-mediated cell migration

Abstract

Abstract Background Cell migration is a fundamental biological process essential for embryonic development and hematopoiesis. In a shRNA screen, we identified the TRAM-LAG1-CLN8 domain-containing transmembrane protein TMEM56 as a previously uncharacterized regulator of stromal cell-derived factor 1 (SDF-1)-mediated cell migration. This study investigates the molecular mechanisms underlying TMEM56 function. Results TMEM56 is expressed in both murine embryonic and adult tissues, with enrichment in hematopoietic stem and erythroid progenitor cells. Lipidomic analysis reveals that TMEM56 modulates ceramide metabolism, particularly affecting levels of hexosylated ceramides. Co-immunoprecipitation assays indicate that TMEM56 physically interacts with ceramide synthase 2 (CerS2), suggesting a role in lipid signaling pathways. Conclusion Our findings identify TMEM56 as a key regulator of cell migration, linking lipid metabolism with hematopoietic and developmental processes. These results provide novel insights into the molecular mechanisms governing migration.

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Cite This Study

Dorschner et al. (2026) studied this question.

synapsesocial.com/papers/69fbe2f2164b5133a91a24fchttps://doi.org/10.1186/s12915-026-02614-7
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