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Related Concept Videos

Proliferative Phase01:20

Proliferative Phase

The proliferative phase typically occurs after menstruation and lasts between 6 to 13 days in a standard 28-day cycle. This phase involves the reconstruction of the endometrium, guided by estrogen produced by the developing ovarian follicle.
Notably, the stratum basale, the basal layer of the endometrium, including the basal parts of the uterine glands, remains unaffected by menstruation. Stem cells in this layer undergo mitosis, regenerating the stratum functionalis and thickening the...
Oogenesis02:07

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...

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Related Experiment Video

Updated: May 30, 2026

Generation of Multicellular Human Primary Endometrial Organoids
09:20

Generation of Multicellular Human Primary Endometrial Organoids

Published on: October 4, 2019

Generating receptive endometrium in Asherman's syndrome.

Caroline E Gargett1, David L Healy

  • 1The Ritchie Centre, Monash Institute of Medical Research, Clayton Road, Victoria, Australia.

Journal of Human Reproductive Sciences
|July 21, 2011
PubMed
Summary

Bone marrow stem cells may regenerate thin endometria, aiding pregnancy. Researchers explored if these cells or endometrial damage triggered the regenerative response.

Keywords:
Adult stem cellsAsherman's syndromebone marrowendometrial stem cellsendometriumregenerationtransplant

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Area of Science:

  • Reproductive medicine
  • Stem cell biology
  • Endometrial regeneration

Background:

  • Thin endometrium poses a significant challenge in reproductive medicine, often refractory to standard estrogen therapy.
  • Endometrial regeneration is crucial for successful implantation and pregnancy.
  • Bone marrow stem/progenitor cells are being investigated for their regenerative potential in various tissues.

Purpose of the Study:

  • To investigate the potential of intrauterine bone marrow stem/progenitor cell administration in regenerating a thin endometrium.
  • To explore the mechanisms underlying endometrial regeneration in a patient with refractory thin endometrium.
  • To determine whether exogenous stem cells or endogenous repair mechanisms were primarily responsible for endometrial recovery.

Main Methods:

  • Administration of bone marrow stem/progenitor cells into the uterine cavity.
  • Concurrent curettage procedure performed on the patient.
  • Monitoring of endometrial thickness and response to treatment.

Main Results:

  • Successful regeneration of the endometrium was observed following stem cell administration.
  • The regenerated endometrium was sufficient to support a pregnancy.
  • The precise contribution of exogenous stem cells versus endogenous repair stimulated by curettage remains to be fully elucidated.

Conclusions:

  • Intrauterine stem cell therapy shows promise for treating thin endometrium.
  • Endometrial regeneration may involve a combination of exogenous stem cell action and endogenous repair mechanisms.
  • Further research is needed to differentiate the roles of stem cells and local injury in endometrial repair.