Evidence map›Paper›PMID 18299350›Full record

ArticleThe Journal of cell biology2008

Integration of Golgi trafficking and growth factor signaling by the lipid phosphatase SAC1.

Anastasia Blagoveshchenskaya, Fei Ying Cheong, Holger M Rohde, Greta Glover, Andreas Knödler, Teresa Nicolson, Guido Boehmelt, Peter Mayinger

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

90 citing papers in PubMed, 151 citations in OpenAlex.

  1. Trial
  2. Subcellular Cartography of the Phosphoinositide Multiverse.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2026
    Review
  3. Golgi Drivers of Cancer.Sub-cellular biochemistry · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Regulation of phosphoinositide metabolism in Apicomplexan parasites.Frontiers in cell and developmental biology · 2023
    Review
  15. Review
  16. Phosphoinositides as membrane organizers.Nature reviews. Molecular cell biology · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. Review

30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Anastasia BlagoveshchenskayaDivision of Nephrology and Hypertension, Oregon Health and Science University, Portland, OR 97239.
Fei Ying Cheong
Holger M Rohde
Greta Glover
Andreas Knödler
Teresa Nicolson
Guido Boehmelt
Peter Mayinger
Hypertension Institute · USBoehringer Ingelheim (Austria) · ATHoward Hughes Medical Institute · US

Funding

Characterization of Sacl lipid phosphatasesR01GM071569 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MAYINGER, PETER J · 2005 to 2009
$1.6M
NIGMS NIH HHS GM071569NIGMS NIH HHS R01 GM071569
6 · The paper itself

Abstract

When a growing cell expands, lipids and proteins must be delivered to its periphery. Although this phenomenon has been observed for decades, it remains unknown how the secretory pathway responds to growth signaling. We demonstrate that control of Golgi phosphatidylinositol-4-phosphate (PI(4)P) is required for growth-dependent secretion. The phosphoinositide phosphatase SAC1 accumulates at the Golgi in quiescent cells and down-regulates anterograde trafficking by depleting Golgi PI(4)P. Golgi localization requires oligomerization of SAC1 and recruitment of the coat protein (COP) II complex. When quiescent cells are stimulated by mitogens, SAC1 rapidly shuttles back to the endoplasmic reticulum (ER), thus releasing the brake on Golgi secretion. The p38 mitogen-activated kinase (MAPK) pathway induces dissociation of SAC1 oligomers after mitogen stimulation, which triggers COP-I-mediated retrieval of SAC1 to the ER. Inhibition of p38 MAPK abolishes growth factor-induced Golgi-to-ER shuttling of SAC1 and slows secretion. These results suggest direct roles for p38 MAPK and SAC1 in transmitting growth signals to the secretory machinery.

Indexed as

AnimalsChlorocebus aethiopsCOP-Coated VesiclesCOS CellsEndoplasmic ReticulumEnzyme InhibitorsGolgi ApparatusHumansIntercellular Signaling Peptides and ProteinsMembrane ProteinsMiceMitogensNIH 3T3 Cellsp38 Mitogen-Activated Protein KinasesPhosphatidylinositol PhosphatesProtein TransportEnzyme InhibitorsIntercellular Signaling Peptides and ProteinsMembrane ProteinsMitogensp38 Mitogen-Activated Protein Kinasesphosphatidylinositol 4-phosphatePhosphatidylinositol PhosphatesSac1 protein, mammalian

Identifiers

PMID18299350
PMCPMC2265582
OpenAlexW2158422128

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.