Evidence map›Paper›PMID 30760704›Full record

ArticleNature communications2019

KDEL receptor regulates secretion by lysosome relocation- and autophagy-dependent modulation of lipid-droplet turnover.

Diego Tapia, Tomás Jiménez, Constanza Zamora, Javier Espinoza, Riccardo Rizzo, Alexis González-Cárdenas, Danitza Fuentes, Sergio Hernández, Viviana A Cavieres, Andrea Soza and 8 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Mechanisms and implications of podocyte autophagy in chronic kidney disease.American journal of physiology. Renal physiology · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. [Type III secretory protein SINC ofNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. The Function of KDEL Receptors as UPR Genes in Disease.International journal of molecular sciences · 2021
    Review
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

18 authors at 6 institutions in 2 countries.

Diego TapiaCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Tomás JiménezCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Constanza ZamoraCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Javier EspinozaDepartamento de Ciencias Biologicas, Facultad de Ciencias de la Vida, Universidad Andrés Bello, Quillota 980, Viña del Mar, 2520000, Chile.
Riccardo RizzoConsiglio Nazionale delle Ricerche (CNR), Istituto di Biochimica delle Proteine (IBP), Via Pietro Castellino 111, 80131, Napoli, Italy.
Alexis González-CárdenasInstituto de Fisiología, Facultad de Medicina, Universidad Austral de Chile, 5110566, Valdivia, Chile.
Danitza FuentesDepartamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, 8331150, Santiago, Chile.
Sergio HernándezCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Viviana A CavieresCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Andrea SozaCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Fanny GuzmánFraunhofer Chile Research, 7550296, Santiago, Chile.
Gloria ArriagadaDepartamento de Ciencias Biologicas, Facultad de Ciencias de la Vida, Universidad Andrés Bello, Quillota 980, Viña del Mar, 2520000, Chile.ORCID http://orcid.org/0000-0002-9935-0451
María Isabel YuseffDepartamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, 8331150, Santiago, Chile.ORCID http://orcid.org/0000-0001-8172-3785
Gonzalo A MardonesCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Patricia V BurgosCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Alberto LuiniConsiglio Nazionale delle Ricerche (CNR), Istituto di Biochimica delle Proteine (IBP), Via Pietro Castellino 111, 80131, Napoli, Italy.
Alfonso GonzálezCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile.
Jorge CancinoCentro de Biología Celular y Biomedicina (CEBICEM), Facultad de Medicina y Ciencia, Universidad San Sebastián, Lota 2465, 7510157, Santiago, Chile. jorge.cancino@uss.cl.
Pontificia Universidad Católica de Chile · CLUniversidad Andrés Bello · CLAustral University of Chile · CLInstitute of Protein Biochemistry · ITSan Sebastián University · CLFraunhofer Chile Research Foundation · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inter-organelle signalling has essential roles in cell physiology encompassing cell metabolism, aging and temporal adaptation to external and internal perturbations. How such signalling coordinates different organelle functions within adaptive responses remains unknown. Membrane traffic is a fundamental process in which membrane fluxes need to be sensed for the adjustment of cellular requirements and homeostasis. Studying endoplasmic reticulum-to-Golgi trafficking, we found that Golgi-based, KDEL receptor-dependent signalling promotes lysosome repositioning to the perinuclear area, involving a complex process intertwined to autophagy, lipid-droplet turnover and Golgi-mediated secretion that engages the microtubule motor protein dynein-LRB1 and the autophagy cargo receptor p62/SQSTM1. This process, here named 'traffic-induced degradation response for secretion' (TIDeRS) discloses a cellular mechanism by which nutrient and membrane sensing machineries cooperate to sustain Golgi-dependent protein secretion.

Indexed as

AutophagyCell Line, TumorCell NucleusDyneinsEndoplasmic ReticulumGolgi ApparatusHeLa CellsHumansLipid DropletsLysosomesMicroscopy, Electron, TransmissionMicrotubulesProtein TransportReceptors, PeptideSequestosome-1 ProteinSignal TransductionDyneinsKDEL receptorReceptors, PeptideSequestosome-1 ProteinSQSTM1 protein, human

Identifiers

PMID30760704
PMCPMC6374470
OpenAlexW2912439423

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.