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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here, we present a protocol to isolate and culture rat endometrial epithelial stem cells (reESCs), generating rat endometrial organoids. This method facilitates in vitro studies of endometrial diseases, enabling gene editing and other cellular manipulations.

Abstract

Endometrial organoids offer valuable insights into the development and pathophysiology of endometrial diseases and serve as platforms for drug testing. While human and mouse endometrial organoids have been developed, research on rat endometrial organoids remains limited. Given that rats can better simulate certain endometrial pathologies, such as intrauterine adhesions, this study aimed to establish rat endometrial organoids. We present a detailed protocol for the isolation and culture of rat endometrial epithelial stem cells (reESCs) and the generation of rat endometrial organoids. Using a refined reESCs expansion medium, we successfully isolated and stably expanded reESCs, demonstrating their long-term culture potential. The reESC-generated organoids exhibited typical structural and functional characteristics of the endometrium, including hormone responsiveness. Our results showed that rat endometrial organoids could be cultured over a long term with stable proliferation, maintaining the glandular structure, cell polarity, and functional characteristics of the endometrial epithelium. This novel rat-derived endometrial organoid model provides a valuable platform for studying endometrial diseases and testing therapeutic interventions, with potential applications across various mammalian species.

Introduction

The endometrium, a versatile and regenerative tissue in the human body, undergoes periodic shedding, regeneration, and differentiation under the influence of ovarian hormones1. Abnormalities in the endometrium are linked to various female reproductive system diseases, such as endometriosis, endometrial cancer, and infertility2. The lack of reliable research models for the endometrium hampers in-depth studies of the pathogenesis, clinical diagnosis, and treatment of these diseases. While cell lines and animal models are commonly utilized for endometrial research, challenges such as phenotypic instabi....

Protocol

Six 7/8-week-old female Sprague-Dawley rats weighing 200-250 g were used in this work. The rats were housed in a climate-controlled animal facility with ad libitum access to food and water. All experimental procedures involving animals were conducted in adherence to the Institutional Guidelines for the Care and Use of Laboratory Animals and were approved by the institutional review board for animal experiments at the Research Ethics Committee of the Meizhou People's Hospital.

The .......

Representative Results

The reESCs and rat uterus organoids were established from six female Sprague-Dawley rats weighing between 200 g and 250 g following the protocol outlined in Figure 1. Drawing on the success of the long-term culture of human endometrial epithelial stem cells, the REEM formulation predominantly consisted of Y27632, A8301, and CHIR99021. To stabilize the reESCs in vitro, we initially isolated endometrial cells from rat endometrium using enzymatic and mechanical techniques. Flow cytomet.......

Discussion

In this study, we have described a straightforward method for isolating and culturing rat endometrial epithelial stem cells (reESCs) and refined the previously established ex vivo system for human endometrial epithelial stem cells8. Our approach utilizes a small molecule culture medium containing Y27632, A8301, and CHIR99021 as core components to enable stable and long-term ex vivo culture. Moreover, we successfully generated rat endometrial organoids in real time using reESCs. T.......

Acknowledgements

This work was supported by GuangDong Basic and Applied Basic Research Foundation (2023A1515110760).

....

Materials

NameCompanyCatalog NumberComments
Anti-CD15 (SSEA-1)Abcamab135377Rabbit, 1:200 (IHC)
Anti-Estrogen Receptor alphaAbcamab32063Rabbit, 1:200 (IHC)
Anti-pan CytokeratinAbcamab7753Mouse, 1:250 (IHC)
Anti-Progesterone ReceptorAbcamab101688Rabbit, 1:200 (IHC)
Anti-Ki67Abcamab279653Mouse, 1:250 (IHC)
A8301TargetMol909910-43-6
β-EstradiolMerckE8875
Cell Counting Kit-8BeyotimeC0038
CD9BioLegend1098191:20 (FC), Pacific Blue
CD24BioLegend1018061:20 (FC), FITC
CD31BioLegend3031201:20 (FC), APC
CD45BioLegend3017031:20 (FC), PE
CHIR99021TargetMolCT99021
Cultrex Organoid Harvesting SolutionR&D Systems3700-100-01
Cy3 TSA Fluorescence System KitAPExBIOK1051
Cy5 TSA Fluorescence System KitAPExBIOK1052
DAPISigmaD95421 μg/mL
DMEM/F-12Invitrogen11330032
EpCAMBioLegend3698031:20 (FC), PerCP
Fluorescein TSA Fluorescence System KitAPExBIOK1050
Goat anti-Rabbit IgG, Alexa Fluor 488InvitrogenA-110081:500
Goat anti-Mouse IgG, Alexa Fluor 555InvitrogenA-214221:500
Goat Anti-rabbit IgG/HRP antibodyAPExBIObs-0295G-HRP
Knockout serum replacementInvitrogen10828028
MatrigelCorning356234
PrimeScript RT Master MixTakaraRR063A
ProgesteroneMerck57-83-0
Sprague-Dawley rat Shanghai JieSiJie Laboratory Animals Co., LTD, China
SSEA-1BioLegend3230471:20 (FC), APC
TB Green Fast qPCR MixTakaraRR820A
TriZOLInvitrogen15596026CNRNA extraction
u-Slide 8-well platesIbidi80827
Y27632TargetMol146986-50-7
qPCR primers of target genes 
GenesCompanySequences
rat GAPDH FSangon biotechGACATGCCGCCTGGAGAAAC
rat GAPDH RSangon biotechAGCCCAGGATGCCCTTTAGT
rat Nanog FSangon biotechGACTAGCAACGGCCTGACTCA
rat Nanog R Sangon biotechCTGCAATGGATGCTGGGATA
rat Sox2 FSangon biotechATTACCCGCAGCAAAATGAC
rat Sox2 RSangon biotechATCGCCCGGAGTCTAGTTCT
rat Oct4 FSangon biotechCCCAGCGCCGTGAAGTTGGA
rat Oct4 RSangon biotechACCTTTCCAAAGAGAACGCCCA
GG

References

  1. Jabbour, H. N., Kelly, R. W., Fraser, H. M., Critchley, H. O. Endocrine regulation of menstruation. Endocr Rev. 27 (1), 17-46 (2006).
  2. Garcia-Alonso, L., et al. Mapping the temporal and spatial dynamics of the human endometrium i....

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