Impaired retrograde membrane traffic through endosomes in a mutant CHO cell defective in phosphatidylserine synthesis

Shoken Lee, Yasunori Uchida, Kazuo Emoto, Masato Umeda, Osamu Kuge, Tomohiko Taguchi, Hiroyuki Arai

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)


Phosphatidylserine (PS), a relatively minor constituent in the plasma membrane (PM), participates in various cellular processes such as clearance of apoptotic cells and recruitment of signaling molecules. PS also localizes in the membranes of endocytic organelles, such as recycling endosomes (REs). We recently showed that in REs, PS binds to the pleckstrin homology (PH) domain of evectin-2, thereby regulating retrograde traffic from REs to the Golgi. However, direct evidence that PS has a role in retrograde traffic is lacking. Here, we examined the contribution of PS to endosomal membrane traffic by exploiting a mutant CHO cell line (PSA-3) that is defective in PS synthesis. In PSA-3 cells, the Golgi localization of TGN38, a protein that circulates between the Golgi and the PM through endosomes by retrograde traffic, was abolished, whereas the localizations of other organelle markers remained unchanged. Increasing the cellular PS level by adding ethanolamine to the culture medium restored the Golgi localization of TGN38. Tracking the endocytic fate of cell surface TGN38 that was labeled by anti-TGN38 antibody showed that retrograde transport of TGN38 was impaired at endosomes, not at the PM. These findings provide direct evidence that intracellular PS is required for retrograde traffic through endosomes.

Original languageEnglish
Pages (from-to)728-736
Number of pages9
JournalGenes to Cells
Issue number8
Publication statusPublished - 2012 Aug
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Cell Biology


Dive into the research topics of 'Impaired retrograde membrane traffic through endosomes in a mutant CHO cell defective in phosphatidylserine synthesis'. Together they form a unique fingerprint.

Cite this