NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE236132 Query DataSets for GSE236132
Status Public on Jan 16, 2024
Title Nutrient-derived signals regulate eosinophil adaptation to the small intestine
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Eosinophils are commonly regarded as effector cells of type 2 immunity, yet they also accumulate in certain tissues during homeostasis - particularly in the gastrointestinal tract. Our understanding of the processes that govern homeostatic eosinophil accumulation and tissue-specific adaptation, and their functional significance, remains very limited. Here, we investigated how eosinophils adapt to the small intestine microenvironment and the local signals that regulate this process. We observed that eosinophils gradually migrate up the crypt-villus axis, giving rise to a villus-resident subpopulation with a distinct transcriptional signature. Genetic deficiency of eosinophils resulted in a reduction of villus area, as well as a reduction of multiple other immune cell populations, demonstrating their diverse functions in this environment. We determined that retinoic acid receptor signaling is specifically required for the maintenance of villus-resident eosinophils, while IL-5 is largely dispensable outside of its canonical role in eosinophil production. In addition, we unexpectedly found that high protein diet suppresses the accumulation of villus-resident eosinophils. Purified amino acids were sufficient for this effect, which was a consequence of accelerated eosinophil turnover within the tissue microenvironment and not due to altered development in the bone marrow. Our study provides new insight into the process of eosinophil adaptation to the small intestine and its dependence on nutrient-derived signals.
 
Overall design Small intestine eosinophil populations (a4b7+, a4b7- CD22-, and CD22+) from wild type female B6 mice were isolated by FACS and their transcriptomes were analyzed by RNA-Seq (4 biological replicates per condition)
 
Contributor(s) Kutyavin VI, Korn LL, Medzhitov R
Citation(s) 38271336
Submission date Jun 29, 2023
Last update date Feb 14, 2024
Contact name Vassily Igor Kutyavin
E-mail(s) vassily.kutyavin@gmail.com
Organization name Yale University
Department Immunobiology
Lab Ruslan Medzhitov Lab
Street address 1 Gilbert St
City New Haven
State/province CT
ZIP/Postal code 06519
Country USA
 
Platforms (1)
GPL30172 NextSeq 2000 (Mus musculus)
Samples (12)
GSM7518689 a4b7+ Eos sample 1
GSM7518690 a4b7+ Eos sample 2
GSM7518691 a4b7+ Eos sample 3
Relations
BioProject PRJNA989113

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE236132_RNA_Seq_Processed_data_1._NormalizedCounts.txt.gz 2.1 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap