Evidence map›Paper›PMID 42329216›Full record

ArticleJournal of leukocyte biology2026

An optimized method to differentiate HL60 cells into neutrophil-like cells.

Samuel P Collie, Grant Yu, Suraj S Rawat, Catharina Rypstra, Carole A Parent

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Samuel P CollieCellular and Molecular Biology Program, University of Michigan Medical School, 1135 Catherine St., Ann Arbor, MI 48109, USA.
Grant YuCollege of Literature, Science, and Arts, University of Michigan, 500 S State St., Ann Arbor, MI 48109, USA.
Suraj S RawatLife Sciences Institute, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI 48109, USA.
Catharina RypstraLife Sciences Institute, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI 48109, USA.
Carole A ParentLife Sciences Institute, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI 48109, USA.ORCID 0000-0002-1518-1452

Funding

American Heart Association AWD025905National Institute of HealthT32 training program in Cell and Molecular biology GM145470T32 training program in Cell and Molecular biology R01AI152517University of Michigan School of Medicine
6 · The paper itself

Abstract

The HL60 promyelocytic leukemia cell line is widely used to investigate neutrophil biology due to its genetic tractability and accessibility. HL60 cells can be differentiated into neutrophil-like cells using all-trans retinoic acid (ATRA) or dimethyl sulfoxide (DMSO) treatment. However, these approaches produce cells that lack critical features of mature granulocytes, such as robust chemotaxis with ATRA treatment or multilobed nuclear morphology with DMSO treatment. To overcome these limitations, we developed a sequential differentiation protocol-ATRA for 1 d followed by DMSO for 4 d (A1D4)-which yields neutrophil-like cells that more faithfully recapitulate the morphology and functionality of mature human neutrophils. A1D4-differentiated HL60 cells display segmented nuclei with low lamin A/C expression and demonstrate strong chemotactic, oxidative burst, and phagocytic activity. This protocol combines the advantages of treatment with the individual compounds, producing cells that closely mimic primary human neutrophils in both phenotype and function.

Indexed as

Cell DifferentiationNeutrophilsChemotaxisDimethyl SulfoxideHL-60 CellsHumansPhagocytosisRespiratory BurstTretinoinDimethyl SulfoxideTretinoinchemotaxisdifferentiationHL60 cellsneutrophilsnucleus

Identifiers

PMID42329216
PMCPMC13345858

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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.