Evidence map›Paper›PMID 35767604›Full record

ArticleScience advances2022

Profiling of mature-stage human breast milk cells identifies six unique lactocyte subpopulations.

John P Gleeson, Namit Chaudhary, Katherine C Fein, Rose Doerfler, Patricia Hredzak-Showalter, Kathryn A Whitehead

Abstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
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  5. Methods for Preserving Human Milk Cellular and Milk Fat Globule RNA.Journal of mammary gland biology and neoplasia · 2026
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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

6 authors.

John P GleesonDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0003-2917-6758
Namit ChaudharyDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Katherine C FeinDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0002-3430-9191
Rose DoerflerDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Patricia Hredzak-ShowalterDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0003-2125-2904
Kathryn A WhiteheadDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0002-0100-7824

Funding

Fate, Function and Genetic Engineering of Breast Milk Cells for Infant TherapyDP2HD098860 · NICHD · CARNEGIE-MELLON UNIVERSITY · PI WHITEHEAD, KATHRYN A. · 2018 to 2021
$2.4M
NICHD NIH HHS DP2 HD098860
6 · The paper itself

Abstract

Breast milk is chock-full of nutrients, immunological factors, and cells that aid infant development. Maternal cells are the least studied breast milk component, and their unique properties are difficult to identify using traditional techniques. Here, we characterized the cells in mature-stage breast milk from healthy donors at the protein, gene, and transcriptome levels. Holistic analysis of flow cytometry, quantitative polymerase chain reaction, and single-cell RNA sequencing data identified the predominant cell population as epithelial with smaller populations of macrophages and T cells. Two percent of epithelial cells expressed four stem cell markers: SOX2, TRA-1-60, NANOG, and SSEA4. Furthermore, milk contained six distinct epithelial lactocyte subpopulations, including three previously unidentified subpopulations programmed toward mucosal defense and intestinal development. Pseudotime analysis delineated the differentiation pathways of epithelial progenitors. Together, these data define healthy human maternal breast milk cells and provide a basis for their application in maternal and infant medicine.

Indexed as

Milk, HumanTranscriptomeCell DifferentiationChildEpithelial CellsFemaleHumansStem Cells

Identifiers

PMID35767604
PMCPMC9242445

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.