Evidence map›Paper›PMID 42589195›Full record

ArticleBiology2026

Single-Nucleus Transcriptomics Reveals Granulosa Cell Heterogeneity and Microenvironmental Remodeling Across Bovine Ovarian States.

Yanchun Bao, Fengying Ma, Xiaoxia Qi, Mingjuan Gu, Lin Zhu, Caixia Shi, Risu Na, Wenguang Zhang

Abstract read
In one paragraph

Article in Biology, 2026. 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

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

8 authors.

Yanchun BaoCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.
Fengying MaCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.
Xiaoxia QiInner Mongolia Saikexing Livestock Breeding and Reproductive Biotechnology Research Institute Co., Ltd., Hohhot 011517, China.
Mingjuan GuCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.ORCID 0000-0002-8244-9519
Lin ZhuCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.
Caixia ShiCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.
Risu NaCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.
Wenguang ZhangCollege of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, China.

Funding

Double First-Class Construction Fund for the Discipline of Animal ScienceNational Dairy Technology Innovation Center Sub-project 2023-JSGG-2Technology Plan Project in Inner Mongolia Autonomous Region 2023YFHH0058the Inner Mongolia Autonomous Region Project under the Open Competition Mechanism 2026KJTW0001
6 · The paper itself

Abstract

Ovarian function is essential for fertility in dairy cattle, yet the cellular and molecular features associated with physiological ovarian states and ovarian dysfunction remain incompletely characterized. In this study, serum and follicular-fluid hormone measurements showed distinct endocrine profiles among ovarian states, and the follicular-fluid estrogen to progesterone was highest during the follicular phase and lowest in luteal and luteal cystic ovaries. Then, single-nucleus RNA sequencing was performed on ovarian tissues from 18 Holstein cows representing follicular, luteal, mid-gestation pregnancy, inactive, and luteal cystic states. After quality control, 154,054 nuclei were retained for cell-type annotation, granulosa cell (GC) subclustering, trajectory inference, co-expression analysis, ligand-receptor and ligand-target prediction, and transcriptome-based metabolic flux estimation. Twenty-seven ovarian cell clusters and five GC subtypes were identified, with state-associated variation in relative nuclear composition and transcriptional profiles. Luteal cystic ovaries showed a higher relative representation of immune cells and enrichment of inflammation-related transcriptional signatures, whereas inactive ovaries exhibited lower levels of predicted intercellular communication. GC analyses indicated differences among ovarian states in transcriptional programs related to proliferation, steroidogenesis, extracellular-matrix organization, inflammation, and metabolism. Transcriptome-based metabolic inference further suggested subtype-associated variation in tricarboxylic acid cycle, lipid, polyamine, phosphoinositide, and gamma-aminobutyric acid-related pathways. This study provides a multi-state single-nucleus transcriptomic resource for bovine ovarian research and identifies candidate cell populations and molecular features for future experimental validation.

Indexed as

Bos tauruscell-cell communicationgranulosa cellsmetabolic reprogrammingovarysingle-nucleus RNA sequencing

Identifiers

PMID42589195
PMCPMC13464624

What Socratic 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 Socratic graph.