Evidence map›Paper›PMID 22120531›Full record

ArticleMolecular and cellular biochemistry2012

Intracellular trafficking and secretion of mouse mesencephalic astrocyte-derived neurotrophic factor.

Kentaro Oh-Hashi, Kensuke Tanaka, Hisashi Koga, Yoko Hirata, Kazutoshi Kiuchi

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

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  16. A soluble endoplasmic reticulum factor as regenerative therapy for Wolfram syndrome.Laboratory investigation; a journal of technical methods and pathology · 2020
    Article
  17. Article
  18. Article
  19. Discovery of endoplasmic reticulum calcium stabilizers to rescue ER-stressed podocytes in nephrotic syndrome.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  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

5 authors at 2 institutions in 1 country.

Kentaro Oh-HashiDepartment of Biomolecular Science, Faculty of Engineering, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. oohashi@gifu-u.ac.jp
Kensuke Tanaka
Hisashi Koga
Yoko Hirata
Kazutoshi Kiuchi
Gifu University · JPKazusa DNA Research Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, mesencephalic astrocyte-derived neurotrophic factor (MANF) has been reported to prevent cell death under some pathophysiological conditions. MANF, also referred to as arginine rich, mutated in early stage of tumors (Armet), was identified as an endoplasmic reticulum (ER) stress-inducible factor. Using RT-PCR, we found two variants of MANF mRNA: wild type, which contains exon 1 (wt-MANF), and one lacking exon 1, which is presumably not secreted (ΔΝ-MANF) in Neuro2a cells. The latter has a putative translational start site upstream of the second exon in the mouse MANF gene. Comparing the expression of wt-MANF with that of ΔΝ-MANF, we found that the amount of intracellular ΔΝ-MANF was much lower than that of wt-MANF. Furthermore, ΔΝ-MANF was not detected in the culture medium after its transient transfection into Neuro2a cells. Deletion of several α-helices of mouse MANF decreased its intracellular stability and secretion. Secretion of wt-MANF was almost completely inhibited by either treatment with brefeldin A (BFA), which disrupts the Golgi apparatus structure, or overexpression of a dominant negative Sar1 (Sar1[H79G]), which is reported to impair COPII-mediated transport from the ER to the Golgi apparatus. In addition, the enforced expression of glucose-regulated protein 78 kDa (GRP78) attenuated the secretion of wt-MANF and led to its intracellular accumulation. MANF lacking the four C-terminal amino acids (ΔC-MANF) accumulated at low levels in the cells, but its intracellular level was increased by GRP78 overexpression. The amount of ΔC-MANF in the culture medium was partially down-regulated after co-transfection of GRP78. Substitution of the amino acids RTDL at the C-terminus of mouse MANF with KDEL, the canonical ER localization signal in GRP78, markedly decreased MANF secretion and its secretion was further attenuated by GRP78 overexpression. Taken together, our data show that the secretion of MANF is regulated via COPII-mediated transport and that its C-terminus could be responsible for its retention in the ER through GRP78. The alternate isotype, ΔΝ-MANF, may be less stable in cells than wt-MANF and may not be secreted extracellularly.

Indexed as

Amino Acid SequenceAnimalsBrefeldin ACell Line, TumorCOP-Coated VesiclesEndoplasmic ReticulumEndoplasmic Reticulum Chaperone BiPExonsGolgi ApparatusHeat-Shock ProteinsHEK293 CellsHumansMiceMolecular Sequence DataMonomeric GTP-Binding ProteinsNerve Growth FactorsBrefeldin AEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHSPA5 protein, humanHspa5 protein, mouseMANF protein, mouseMonomeric GTP-Binding ProteinsNerve Growth FactorsRNA, MessengerThapsigargin

Identifiers

PMID22120531
OpenAlexW1991514065

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.