Evidence map›Paper›PMID 38504138›Full record

ReviewNature protocols2024

Stress-free single-cell transcriptomic profiling and functional genomics of murine eosinophils.

Costanza Borrelli, Alessandra Gurtner, Isabelle C Arnold, Andreas E Moor

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature protocols, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  9. Emerging Roles of Eosinophils in Bone.Current osteoporosis reports · 2025
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  11. Observational
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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

4 authors at 2 institutions in 1 country.

Costanza Borrelli *Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0002-8732-773X
Alessandra Gurtner *Institute of Experimental Immunology, University of Zürich, Zürich, Switzerland.
Isabelle C ArnoldInstitute of Experimental Immunology, University of Zürich, Zürich, Switzerland. arnold@immunology.uzh.ch.ORCID 0000-0001-8679-9666
Andreas E MoorDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland. andreas.moor@bsse.ethz.ch.ORCID 0000-0001-8715-8449
ETH Zurich · CHUniversity of Zurich · CH

Funding

Leona M. and Harry B. Helmsley Charitable Trust (Helmsley Charitable Trust) 1903-03791Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) PCEFP3_ 181249Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) PCEFP3_187021Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) TMCG-3_213857Vontobel-Stiftung (Vontobel Foundation) 1120/2022
6 · The paper itself

Abstract

Eosinophils are a class of granulocytes with pleiotropic functions in homeostasis and various human diseases. Nevertheless, they are absent from conventional single-cell RNA sequencing atlases owing to technical difficulties preventing their transcriptomic interrogation. Consequently, eosinophil heterogeneity and the gene regulatory networks underpinning their diverse functions remain poorly understood. We have developed a stress-free protocol for single-cell RNA capture from murine tissue-resident eosinophils, which revealed distinct intestinal subsets and their roles in colitis. Here we describe in detail how to enrich eosinophils from multiple tissues of residence and how to capture high-quality single-cell transcriptomes by preventing transcript degradation. By combining magnetic eosinophil enrichment with microwell-based single-cell RNA capture (BD Rhapsody), our approach minimizes shear stress and processing time. Moreover, we report how to perform genome-wide CRISPR pooled genetic screening in ex vivo-conditioned bone marrow-derived eosinophils to functionally probe pathways required for their differentiation and intestinal maturation. These protocols can be performed by any researcher with basic skills in molecular biology and flow cytometry, and can be adapted to investigate other granulocytes, such as neutrophils and mast cells, thereby offering potential insights into their roles in both homeostasis and disease pathogenesis. Single-cell transcriptomics of eosinophils can be performed in 2-3 d, while functional genomics assays may require up to 1 month.

Indexed as

EosinophilsGene Expression ProfilingSingle-Cell AnalysisAnimalsGenomicsMiceMice, Inbred C57BLTranscriptome

Identifiers

PMID38504138
OpenAlexW4392947530

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.