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Series GSE205992 Query DataSets for GSE205992
Status Public on Jun 21, 2022
Title Human umbilical cord blood-derived MSCs trans-differentiate into endometrial cells and regulate Th17/Treg balance through NF-B signaling in rabbit intrauterine adhesions endometrium [RNA-seq]
Organism Oryctolagus cuniculus
Experiment type Expression profiling by high throughput sequencing
Summary Purpose: The fundamental cause of intrauterine adhesions (IUAs) is the destruction and reduction of stem cells in endometrial basal layer, resulting in endometrial reconstruction very difficult. The purpose of this study was to investigate the effects and underlying mechanism of human umbilical cord blood derived mesenchymal stem cells (hUCB-MSC) on the endometrial reconstruction after transplantation. Methods: hUCB-MSCs were isolated and identified successfully. The rabbit IUA models were established and set five groups (control, 14/28th day after surgery, estrogen and hUCB-MSCs treatment).The number of endometrial glands and the fibrosis rate were evaluated using HE and Masson staining, respectively. Endometrial proliferation, angiogenesis and inflammation was evaluated by immunohistochemical staining of ER, Ki-67and TGF-β1, respectively. Single-cell RNA sequencing (scRNA-seq) was applied to explore the cell differentiation trajectory after hUCB-MSCs transplanted into IUA endometrium. Finally, molecular mechanism of hUCB-MSCs repairing damaged endometrium was investigated by RNA sequencing. Results: After transplantation of the hUCB-MSCs, the increase of endometrial gland number, estrogen receptor(ER) and Ki-67expression,and the decrease of fibrosis rate and TGF-β expression(P<0.05), suggested the endometrial repair, angiogenesis and inflammatory suppression. The therapeutic effect of hUCB-MSCs was significantly improved compared with 28th day after surgery and estrogen group. ScRNA-seq demonstrated that the transplanted hUCB-MSCs can trans-differentiate into endometrial cells: epithelial, fibroblast, and macrophage. RNA Sequencing of six IUA samples further revealed that hUCB-MSCs may regulate Th17/Treg balance through NF-B signaling, thus inhibiting the immune response of damaged endometrium. Conclusions: Our study demonstrated that hUCB-MSCs can repair damaged endometrium through trans-differentiation, immunomodulatory capacities, and NF-κB signaling, suggesting the treatment value of hUCB-MSCs in IUA.
 
Overall design The rabbit IUA samples with and without treated with hUCB-MSCs were used for transcriptome sequencing (3 vs 3)
 
Contributor(s) Hua Q, Zhang Y, Sun L, Wang Y
Citation(s) 35841027
Submission date Jun 13, 2022
Last update date Jul 20, 2022
Contact name Yong Zhang
E-mail(s) zhangyonglzg@zzu.edu.cn
Phone 6719
Organization name Zhengzhou University
Street address Tongbaibei NO.16 Zhongyuan district, Zhengzhou
City Zhengzhou
State/province State...
ZIP/Postal code 450007
Country China
 
Platforms (1)
GPL21255 Illumina HiSeq 2500 (Oryctolagus cuniculus)
Samples (6)
GSM6238804 rabbit IUA sample1 without treated with hUCB-MSCs
GSM6238805 rabbit IUA sample2 without treated with hUCB-MSCs
GSM6238806 rabbit IUA sample3 without treated with hUCB-MSCs
This SubSeries is part of SuperSeries:
GSE205997 Human umbilical cord blood-derived MSCs trans-differentiate into endometrial cells and regulate Th17/Treg balance through NF-B signaling in rabbit intrauterine adhesions endometrium
Relations
BioProject PRJNA848771

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Supplementary file Size Download File type/resource
GSE205992_All_reads_counts.xls.gz 2.5 Mb (ftp)(http) XLS
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Raw data are available in SRA
Processed data are available on Series record

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