Evidence map›Paper›PMID 37609222›Full record

ArticlebioRxiv : the preprint server for biology2023

Single Cell Transcriptomes, Lineage, and Differentiation of Functional Airway Microfold Cells.

Manalee V Surve, Brian Lin, Jennifer L Reedy, Arianne J Crossen, Anthony Xu, Bruce S Klein, Jatin M Vyas, Jayaraj Rajagopal

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Manalee V SurveCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.
Brian LinCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.
Jennifer L ReedyDepartment of Medicine, Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Arianne J CrossenDepartment of Medicine, Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Anthony XuCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.
Bruce S KleinDepartment of Pediatrics, Medicine, and Medical Microbiology and Immunology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
Jatin M VyasDepartment of Medicine, Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
Jayaraj RajagopalCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA.

Funding

PROTECTIVE IMMUNE RESPONSES TO BLASTOMYCES DERMATITIDISR01AI040996 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, BRUCE STEVEN, WUETHRICH, MARCEL · 1997 to 2023
$10.4M
Molecular Pathogenesis of BlastomycosisR37AI035681 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BRUCE Steven KLEIN · 2004 to 2026
$6.9M
Control of Type I Interferon Production in Response to Candida albicansR01AI150181 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Jatin M Vyas · 2020 to 2026
$5.4M
Progenitors, Mechanisms of Differentiation, and Functions of Lung M CellsR01HL164563 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI RAJAGOPAL, JAYARAJ · 2022 to 2025
$3.2M
Functional Role of the Tetraspanin CD82/Kai1 in Innate and Adaptive ImmunityR01AI092084 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2011 to 2015
$2.2M
Mechanisms of vaccine immunity against coccidioidomycosisR01AI168370 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BRUCE Steven KLEIN · 2023 to 2026
$2.2M
Innate Immune Response to Aspergillus fumigatus Cell Wall CarbohydratesK08AI141755 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI REEDY, JENNIFER LYNNE · 2019 to 2022
$799k
Systems Analysis of Innate Immune Responses to Fungal-Derived CarbohydratesR21AI109303 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2015 to 2016
$479k
NHLBI NIH HHS R01 HL164563NIAID NIH HHS K08 AI141755NIAID NIH HHS R01 AI040996NIAID NIH HHS R01 AI092084NIAID NIH HHS R01 AI150181NIAID NIH HHS R01 AI168370NIAID NIH HHS R21 AI109303NIAID NIH HHS R37 AI035681
6 · The paper itself

Abstract

The airway epithelium is frequently exposed to pathogens and allergens, but the cells that are responsible for sampling these inhaled environmental agents have not been fully defined. Thus, there is a critical void in our understanding of how luminal antigens are delivered to the immune cells that drive the appropriate immune defenses against environmental assaults. In this study, we report the first single cell transcriptomes of airway Microfold (M) cells, whose gut counterparts have long been known for their antigen sampling abilities. Given their very recent discovery in the lower respiratory airways, the mechanisms governing the differentiation and functions of airway M cells are largely unknown. Here, we shed light on the pathways of airway M cell differentiation, establish their lineage, and identify a functional M cell-specific endocytic receptor, the complement receptor 2 (CR2). Lastly, we demonstrate that airway M cells can endocytose

Identifiers

PMID37609222
PMCPMC10441290

What OpenQuestion holds

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Registered trials

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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.