Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Dissecting autonomous enzymatic variability in single cells.

Nature communications·2026
Same author

[<sup>177</sup>Lu]Lu-AKIR001 for CD44v6-Positive Pancreatic Cancer: Preclinical Efficacy and Combination Strategies.

Journal of nuclear medicine : official publication, Society of Nuclear Medicine·2026
Same author

A high-resolution spatial map of cilia-associated proteins in the human fallopian tube.

Nature communications·2026
Same author

Testicular organoids formation from leukaemia-infiltrated prepubertal testicular tissue: implications for fertility preservation.

Leukemia·2026
Same author

SHP2 regulates VEGFR2 Y1175/PLCγ signaling to impair tumor endothelial barrier stability.

iScience·2026
Same author

Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients.

Acta neuropathologica communications·2026
Same journal

Defining and characterizing the relevant state variables of the mammalian gut ecosystem.

Cell reports·2026
Same journal

Distinct compositional changes but shared quantitative microbiome and anti-inflammatory modulations by diet.

Cell reports·2026
Same journal

HPD is a copper-binding protein that interacts with DLAT to promote colorectal cancer cuproptosis under copper stress.

Cell reports·2026
Same journal

Rotational trophoblast organoids reveal biomechanical regulation of trophoblast differentiation.

Cell reports·2026
Same journal

Dysregulated calcium signaling underlies hyposalivation and microbial dysbiosis in Down syndrome.

Cell reports·2026
Same journal

Collagen 1-mediated CXCL1 secretion in tumor cells activates fibroblasts to promote radioresistance of esophageal cancer.

Cell reports·2026
See all related articles

Related Experiment Video

Updated: Sep 4, 2025

Adipocyte-Specific ATAC-Seq with Adipose Tissues Using Fluorescence-Activated Nucleus Sorting
11:11

Adipocyte-Specific ATAC-Seq with Adipose Tissues Using Fluorescence-Activated Nucleus Sorting

Published on: March 17, 2023

2.4K

A human adipose tissue cell-type transcriptome atlas.

Marthe Norreen-Thorsen1, Eike Christopher Struck1, Sofia Öling1

  • 1Translational Vascular Research, Department of Clinical Medicine, The Arctic University of Norway, 9019 Tromsø, Norway.

Cell Reports
|July 13, 2022
PubMed
Summary
This summary is machine-generated.

This study deciphers cell-type-specific gene expression in human adipose tissue using bulk RNA sequencing. It identifies thousands of cell-type-enriched transcripts and reveals key drivers of differences between visceral and subcutaneous fat depots.

Keywords:
CP: Cell biologyCP: Molecular biologyRNA-seqadipocytesadipose tissuecell profiling

More Related Videos

Isolation of Adipose Tissue Nuclei for Single-Cell Genomic Applications
07:03

Isolation of Adipose Tissue Nuclei for Single-Cell Genomic Applications

Published on: June 12, 2020

10.0K
Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans
05:59

Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans

Published on: May 3, 2024

830

Related Experiment Videos

Last Updated: Sep 4, 2025

Adipocyte-Specific ATAC-Seq with Adipose Tissues Using Fluorescence-Activated Nucleus Sorting
11:11

Adipocyte-Specific ATAC-Seq with Adipose Tissues Using Fluorescence-Activated Nucleus Sorting

Published on: March 17, 2023

2.4K
Isolation of Adipose Tissue Nuclei for Single-Cell Genomic Applications
07:03

Isolation of Adipose Tissue Nuclei for Single-Cell Genomic Applications

Published on: June 12, 2020

10.0K
Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans
05:59

Author Spotlight: Deciphering the Cellular Mysteries of Intermuscular Adipose Tissue in Humans

Published on: May 3, 2024

830

Area of Science:

  • Adipose tissue biology
  • Transcriptomics
  • Genomics

Background:

  • Single-cell RNA sequencing (scRNA-seq) faces challenges with adipocytes, the main adipose tissue cell type.
  • Adipocyte data is often missing from scRNA-seq studies despite their functional importance.
  • Defining cell-type-specific genes is crucial for understanding tissue function.

Purpose of the Study:

  • To develop a method for profiling cell-type-enriched transcriptomes from unfractionated adipose tissue using bulk RNA sequencing.
  • To identify cell-type-specific genes in human visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT).
  • To uncover sex-specific gene expression patterns and identify drivers of differential gene expression between VAT and SAT.

Main Methods:

  • Analysis of bulk RNA sequencing data from 527 VAT and 646 SAT samples.
  • Identification of cell-type-enriched transcripts across major adipose tissue cell types.
  • Sex-subset analysis and differential expression analysis between SAT and VAT.

Main Results:

  • Identification of over 2,300 cell-type-enriched transcripts.
  • Discovery of a panel of male-only cell-type-enriched genes.
  • Mesothelial cells identified as the primary drivers of gene expression differences between SAT and VAT.

Conclusions:

  • Bulk RNA sequencing provides an accessible method to profile cell-type-enriched transcriptomes in adipose tissue.
  • This study generates a valuable resource and roadmap for adipose tissue biology research.
  • The findings enhance our understanding of adipose tissue heterogeneity and cell-specific functions.