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Bone marrow-derived cell populations in uterine and ectopic endometrium
S Fernández-Shaw1, M T Clarke, B Hicks
1University of Oxford, Nuffield Department of Obstetrics and Gynaecology, John Radcliffe Hospital, Headington, UK.
Human Reproduction (Oxford, England)
|September 1, 1995
Summary
Endometrial tissue, including in endometriosis, contains bone marrow-derived cells. These immune cells in ectopic endometrium suggest similar cell migration and differentiation processes occur in both uterine and ectopic tissues.
Area of Science:
- Immunology
- Gynecology
- Cell Biology
Background:
- The uterine endometrium hosts diverse bone marrow-derived cells, with distinct profiles compared to other tissues.
- Endometriosis may involve altered endometrial phenotypes, potentially influenced by bone marrow-derived cell populations.
Purpose of the Study:
- To investigate the presence and characteristics of bone marrow-derived cells in ectopic endometrial tissue.
- To compare the immune cell populations in normal uterine endometrium with those in ectopic endometrium from women with endometriosis.
Main Methods:
- Flow cytometry analysis of CD45+ cells in uterine and ectopic endometrium.
- Characterization of specific immune cell subsets including T cells, macrophages, and large granular lymphocytes (CD56+).
Main Results:
- Both normal uterine and ectopic endometrium contain CD45+ bone marrow-derived cells, including T cells, macrophages, and CD56+ large granular lymphocytes.
- While cell populations changed cyclically in normal endometrium, ectopic endometrium showed similar cell types without a clear cyclical pattern.
- The frequency of CD45+ cells was comparable between uterine and ectopic endometrium.
Conclusions:
- Ectopic endometrium contains bone marrow-derived cell populations similar to those found in uterine endometrium.
- These findings suggest that common mechanisms of cell migration and differentiation operate in both uterine and ectopic endometrial tissues.
- The presence of these cells may offer insights into the pathogenesis and differentiation of endometriosis.