Evidence map›Paper›PMID 21098683›Full record

ArticlePhysiological genomics2011

Transcription factor MIST1 in terminal differentiation of mouse and human plasma cells.

Benjamin J Capoccia, Jochen K M Lennerz, Andrew J Bredemeyer, Jeffery M Klco, John L Frater, Jason C Mills

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Conditional Loss of Nmp4 in Mesenchymal Stem Progenitor Cells Enhances PTH-Induced Bone Formation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Mist1: a novel nuclear marker for acinic cell carcinoma of the salivary gland.Virchows Archiv : an international journal of pathology · 2019
    Article
  12. Article
  13. Maturity and age influence chief cell ability to transdifferentiate into metaplasia.American journal of physiology. Gastrointestinal and liver physiology · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. MIST1-a novel marker of plasmacytic differentiation.Applied immunohistochemistry & molecular morphology : AIMM · 2012
    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

6 authors at 2 institutions in 1 country.

Benjamin J CapocciaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Jochen K M Lennerz
Andrew J Bredemeyer
Jeffery M Klco
John L Frater
Jason C Mills
Massachusetts General Hospital · USWashington University in St. Louis · US

Funding

TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
MOLECULAR REGULATION OF GASTRIC CHIEF (ZYMOGENIC) CELL DIFFERENTIATIONR01DK079798 · NIDDK · WASHINGTON UNIVERSITY · PI MILLS, JASON C · 2008 to 2012
$1.6M
NCI NIH HHS T32 CA-009547-23NIDDK NIH HHS R01 DK079798NIDDK NIH HHS R01 DK-079798-01
6 · The paper itself

Abstract

Despite their divergent developmental ancestry, plasma cells and gastric zymogenic (chief) cells share a common function: high-capacity secretion of protein. Here we show that both cell lineages share increased expression of a cassette of 269 genes, most of which regulate endoplasmic reticulum (ER) and Golgi function, and they both induce expression of the transcription factors X-box binding protein 1 (Xbp1) and Mist1 during terminal differentiation. XBP1 is known to augment plasma cell function by establishing rough ER, and MIST1 regulates secretory vesicle trafficking in zymogenic cells. We examined morphology and function of plasma cells in wild-type and Mist1(-/-) mice and found subtle differences in ER structure but no overall defect in plasma cell function, suggesting that Mist1 may function redundantly in plasma cells. We next reasoned that MIST1 might be useful as a novel and reliable marker of plasma cells. We found that MIST1 specifically labeled normal plasma cells in mouse and human tissues, and, moreover, its expression was also characteristic of plasma cell differentiation in a cohort of 12 human plasma cell neoplasms. Overall, our results show that MIST1 is enriched upon plasma cell differentiation as a part of a genetic program facilitating secretory cell function and also that MIST1 is a novel marker of normal and neoplastic plasma cells in mouse and human tissues.

Indexed as

Cell DifferentiationAnimalsAntibodiesBasic Helix-Loop-Helix ProteinsChief Cells, GastricDNA-Binding ProteinsFlow CytometryGene Expression RegulationHumansIntracellular MembranesLeukemia, Plasma CellLipopolysaccharidesMicePlasma CellsPromoter Regions, GeneticRegulatory Factor X Transcription FactorsAntibodiesBasic Helix-Loop-Helix ProteinsBHLHA15 protein, humanBhlha15 protein, mouseDNA-Binding ProteinsLipopolysaccharidesRegulatory Factor X Transcription FactorsSyndecan-1Transcription FactorsX-Box Binding Protein 1XBP1 protein, humanXbp1 protein, mouse

Identifiers

PMID21098683
PMCPMC3055710
OpenAlexW1997592537

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.