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From the Department of Microbiology and Immunology,*
Cancer Center, University of Rochester School of Medicine and
Dentistry, Rochester, New York; and the Medical Research
Council,
Reproductive Biology Unit, Center for
Reproductive Biology, Edinburgh, Scotland
Little is known about fibroblasts from the female
reproductive tract, much less whether or not functional subsets
exist. Fibroblasts are key as sentinel cells for recruiting white blood
cells and for wound healing. The purpose of this research was to
evaluate the possibility that functional subsets of fibroblasts exist
in the human female reproductive tract. The strategy used was to define
fibroblast subpopulations based on their surface expression of the Thy
1 antigen. In situ staining of human myometrium and
endometrium showed heterogeneous staining for Thy 1. Freshly derived
strains of fibroblasts from the myometrium and endometrium also
demonstrated heterogeneous Thy 1 expression. For the first
time, using magnetic beading and fluorescence-activated cell
sorting, human myometrial fibroblasts were successfully
separated into functionally unique Thy 1+ and Thy
1- subsets. Both subsets produced the proinflammatory
cytokines interleukin (IL)-6 and IL-8 after IL-1ß
stimulation, but only the Thy 1+ subset produced
MCP-1. Furthermore, only Thy 1+ fibroblasts
up-regulated CD40 surface expression with IL-1ß or interferon-
treatment. Engagement of CD40 in the Thy 1+ subpopulation
induced IL-6, IL-8, and MCP-1. The discovery of
functional subsets of reproductive tract fibroblasts now permits
assessment of their roles in the normal functions of the reproductive
tract and in disease states such as adhesions and
menorrhagia.
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