Evidence map›Paper›PMID 28375676›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2017

Tyrosine Phosphorylation of an Actin-Binding Protein Girdin Specifically Marks Tuft Cells in Human and Mouse Gut.

Daisuke Kuga, Kaori Ushida, Shinji Mii, Atsushi Enomoto, Naoya Asai, Masato Nagino, Masahide Takahashi, Masato Asai

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Regulation of immune responses by tuft cells.Nature reviews. Immunology · 2019
    Review
  11. Article
  12. Article
  13. Luminal chemosensing in the gastroduodenal mucosa.Current opinion in gastroenterology · 2017
    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

8 authors at 1 institution in 1 country.

Daisuke KugaDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kaori UshidaDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinji MiiDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Atsushi EnomotoDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Naoya AsaiDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masato NaginoDivision of Surgical Oncology, Department of Surgery (DK, MN), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masahide TakahashiDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masato AsaiDepartment of Pathology (DK, KU, SM, AE, NA, MT, MA), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuft cells (TCs) are minor components of gastrointestinal epithelia, characterized by apical tufts and spool-shaped somas. The lack of reliable TC-markers has hindered the elucidation of its role. We developed site-specific and phosphorylation-status-specific antibodies against Girdin at tyrosine-1798 (pY1798) and found pY1798 immunostaining of mouse jejunum clearly depicted epithelial cells closely resembling TCs. This study aimed to validate pY1798 as a TC-marker. Double-fluorescence staining of intestines was performed with pY1798 and known TC-markers, for example, hematopoietic-prostaglandin-D-synthase (HPGDS), or doublecortin-like kinase 1 (DCLK1). Odds ratios (ORs) were calculated from cell counts to determine whether two markers were attracting (OR<1) or repelling (OR>1). In consequence, pY1798 signals strongly attracted those of known TC-markers. ORs for HPGDS in mouse stomach, small intestine, and colon were 0 for all, and 0.08 for DCLK1 in human small intestine. pY1798-positive cells in jejunum were distinct from other minor epithelial cells, including goblet, Paneth, and neuroendocrine cells. Thus, pY1798 was validated as a TC-marker. Interestingly, apoptosis inducers significantly increased relative TC frequencies despite the absence of proliferation at baseline. In conclusion, pY1798 is a novel TC-marker. Selective tyrosine phosphorylation and possible resistance to apoptosis inducers implied the activation of certain kinase(s) in TCs, which may become a clue to elucidate the enigmatic roles of TCs. .

Indexed as

AnimalsApoptosisBiomarkersCell ProliferationEpithelial CellsHumansMiceMicrofilament ProteinsPhosphorylationTyrosineVesicular Transport ProteinsBiomarkersCCDC88A protein, humanCcdc88a protein, mouseMicrofilament ProteinsTyrosineVesicular Transport Proteinsbrush cellGirdintuft cell markertyrosine phosphorylation

Identifiers

PMID28375676
PMCPMC5625852
OpenAlexW2604399404

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.