Evidence map›Paper›PMID 32562023›Full record

ArticleCellular and molecular life sciences : CMLS2021

KDEL receptor is a cell surface receptor that cycles between the plasma membrane and the Golgi via clathrin-mediated transport carriers.

Jie Jia, Xihua Yue, Lianhui Zhu, Shuaiyang Jing, Yijing Wang, Bopil Gim, Yi Qian, Intaek Lee

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-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

21 citing papers in PubMed, 51 citations in OpenAlex.

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  16. Selective Secretion of KDEL-Bearing Proteins: Mechanisms and Functions.Frontiers in cell and developmental biology · 2022
    Review
  17. Article
  18. Article
  19. The Function of KDEL Receptors as UPR Genes in Disease.International journal of molecular sciences · 2021
    Review
  20. Article
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 1 institution in 1 country.

Jie Jia *School of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Xihua Yue *School of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Lianhui ZhuSchool of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Shuaiyang JingSchool of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Yijing WangSchool of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Bopil GimSchool of Physical Science and Technology, ShanghaiTech University, Pudong, Shanghai, China.
Yi QianSchool of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China. Qianyi@shanghaitech.edu.cn.
Intaek LeeSchool of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China. Leeintaek@shanghaitech.edu.cn.ORCID http://orcid.org/0000-0003-1084-674X
ShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KDEL receptor cycles between the ER and the Golgi to retrieve ER-resident chaperones that get leaked to the secretory pathway during protein export from the ER. Recent studies have shown that a fraction of KDEL receptor may reside in the plasma membrane and function as a putative cell surface receptor. However, the trafficking itinerary and mechanism of cell surface expressed KDEL receptor remains largely unknown. In this study, we used N-terminally Halo-tagged KDEL receptor to investigate its endocytosis from the plasma membrane and trafficking itinerary of the endocytosed receptor through the endolysosomal compartments. Our results indicate that surface-expressed KDEL receptor undergoes highly complex recycling pathways via the Golgi and peri-nuclear recycling endosomes that are positive for Rab11 and Rab14, respectively. Unexpectedly, KDEL receptor appears to preferentially utilize clathrin-mediated endocytic pathway as well as clathrin-dependent transport carriers for export from the trans-Golgi network. Taken together, we suggest that KDEL receptor may be a bona fide cell surface receptor with a complex, yet well-defined trafficking itinerary through the endolysosomal compartments.

Indexed as

EndocytosisCell Line, TumorCell MembraneClathrinEndosomesGene EditingGolgi ApparatusGreen Fluorescent ProteinsHumansMicroscopy, FluorescenceMutagenesis, Site-DirectedProtein Isoformsrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsReceptors, PeptideRNA InterferenceClathrinenhanced green fluorescent proteinGreen Fluorescent ProteinsKDELR1 protein, humanProtein Isoformsrab11 GTP-Binding ProteinsRab14 protein, humanrab GTP-Binding ProteinsReceptors, PeptideRNA, Small InterferingCaveolaeClathrinEarly endosomesEEA1GolgiKDEL receptorLate endosomesLysosomeMANFMembrane traffickingRab11Rab14Recycling endosomes

Identifiers

PMID32562023
PMCPMC11072833
OpenAlexW3036232620

What OpenQuestion holds

Textmetadata
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.