Evidence map›Paper›PMID 38385029›Full record

ArticleFrontiers in cell and developmental biology2024

Deep learning classification for macrophage subtypes through cell migratory pattern analysis.

Manasa Kesapragada, Yao-Hui Sun, Ksenia Zlobina, Cynthia Recendez, Daniel Fregoso, Hsin-Ya Yang, Elham Aslankoohi, Rivkah Isseroff, Marco Rolandi, Min Zhao and 1 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Neuroprotective Potential ofInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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

11 authors.

Manasa KesapragadaDepartment of Applied Mathematics, Baskin School of Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.
Yao-Hui SunDepartment of Ophthalmology and Vision Science, School of Medicine, University of California, Davis, Sacramento, CA, United States.
Ksenia ZlobinaDepartment of Applied Mathematics, Baskin School of Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.
Cynthia RecendezDepartment of Ophthalmology and Vision Science, School of Medicine, University of California, Davis, Sacramento, CA, United States.
Daniel FregosoDepartment of Dermatology, School of Medicine, UC Davis, Sacramento, CA, United States.
Hsin-Ya YangDepartment of Dermatology, School of Medicine, UC Davis, Sacramento, CA, United States.
Elham AslankoohiDepartment of Electrical and Computer Engineering, Baskin School of Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.
Rivkah IsseroffDepartment of Dermatology, School of Medicine, UC Davis, Sacramento, CA, United States.
Marco RolandiDepartment of Electrical and Computer Engineering, Baskin School of Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.
Min ZhaoDepartment of Ophthalmology and Vision Science, School of Medicine, University of California, Davis, Sacramento, CA, United States.
Marcella GomezDepartment of Applied Mathematics, Baskin School of Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.

Funding

Bioelectricity in Gut Epithelium Drives Pathogenic Bacterial TargetingR21AI156409 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SUN, YAOHUI, ZHAO, MIN · 2021 to 2022
$432k
NIAID NIH HHS R21 AI156409
6 · The paper itself

Abstract

Macrophages can exhibit pro-inflammatory or pro-reparatory functions, contingent upon their specific activation state. This dynamic behavior empowers macrophages to engage in immune reactions and contribute to tissue homeostasis. Understanding the intricate interplay between macrophage motility and activation status provides valuable insights into the complex mechanisms that govern their diverse functions. In a recent study, we developed a classification method based on morphology, which demonstrated that movement characteristics, including speed and displacement, can serve as distinguishing factors for macrophage subtypes. In this study, we develop a deep learning model to explore the potential of classifying macrophage subtypes based solely on raw trajectory patterns. The classification model relies on the time series of x-y coordinates, as well as the distance traveled and net displacement. We begin by investigating the migratory patterns of macrophages to gain a deeper understanding of their behavior. Although this analysis does not directly inform the deep learning model, it serves to highlight the intricate and distinct dynamics exhibited by different macrophage subtypes, which cannot be easily captured by a finite set of motility metrics. Our study uses cell trajectories to classify three macrophage subtypes: M0, M1, and M2. This advancement holds promising implications for the future, as it suggests the possibility of identifying macrophage subtypes without relying on shape analysis. Consequently, it could potentially eliminate the necessity for high-quality imaging techniques and provide more robust methods for analyzing inherently blurry images.

Indexed as

analysis of macrophage trajectory patternsclassification of macrophage subtypes using migration patternscorrelation between cell shape and trajectoriesdeep learning for classification of macrophage subtypesmacrophage polarization

Identifiers

PMID38385029
PMCPMC10879298

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.