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human female
reproductive tract fibroblasts
Departments of 1 Microbiology and Immunology, 2 Environmental Medicine, and 3 Pediatrics and Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Lung Biology and Disease Program, Rochester, New York 14642
A
key role exists for prostaglandins (PGs) in reproductive health,
including fertility and parturition. However, the cellular sources and
regulation of PG production by cyclooxygenase (COX) in the human female
reproductive tract remain poorly understood. We recently reported that
human female reproductive tract fibroblasts are divisible into distinct
subsets based on their Thy-1 surface expression. Herein, we demonstrate
that the expression, induction, and subcellular localization of COX-1
and COX-2 and the downstream PG biosynthesis are markedly different
between these subsets. Specifically, Thy-1+ fibroblasts
highly express COX-1, which is responsible for high-level PGE2 production, a feature usually attributed to the COX-2
isoenzyme. In contrast, COX-2, generally considered an inducible
isoform, is constitutively expressed in the Thy-1
subset,
which only minimally produces PGE2. The intracellular signaling pathways for COX regulation also differ between the subsets.
Determination of differences in signal transduction, COX expression and
localization, and PG production by human reproductive fibroblast
subtypes supports the concept of fibroblast heterogeneity and the
possibility that these subsets may play unique roles in tissue
homeostasis and in inflammation.
inflammation; myometrium; lipid mediators; heterogeneity; prostaglandin; cyclooxygenase
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