Potential Roles of A Special CD8αα+ Cell Population and CC Chemokine TECK in Ovulation Related Inflammation1
It is well known that ovulation may be an inflammatory process. However, it remains elusive how immune cells participate in this process. We have identified a novel CD8αα + population, which resembles tissue DC, in the theca of antral follicles. We further observed a dramatic influx of the CD8αα + c...
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Published in | The Journal of immunology (1950) Vol. 182; no. 1; pp. 596 - 603 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2009
|
Online Access | Get full text |
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Summary: | It is well known that ovulation may be an inflammatory process. However, it remains elusive how immune cells participate in this process. We have identified a novel CD8αα
+
population, which resembles tissue DC, in the theca of antral follicles. We further observed a dramatic influx of the CD8αα
+
cells into the ovulating follicles. This CD8αα
+
population was absent in the ovary of estradiol-induced anovulatory C31F1 mice and sub-fertile athymic nude mice. Expression of a CC chemokine TECK (thymus expressed chemokine) has previously been found in the ovary; we further demonstrated that TECK attracted CD8αα
+
cells into the ovary. Anti-TECK Ab, elicited in the female mice by active immunization, depleted the ovarian CD8αα
+
cells
in vivo
. Mice with a high titer of TECK Ab failed to ovulate after super-ovulation induction. More importantly, the immunized mice had a greatly reduced fertility, which was positively correlated with the Ab titers. Ovarian TECK expression was normal in anovulatory C31F1 mice, suggesting that infertility in the immunized mice is due to a block of CD8αα
+
cell migration. Finally, the origin of ovarian CD8αα
+
cells was explored. Upon being transferred, thymic CD8α
+
cells were able to home to the theca of follicles in the recipients. Thus, ovarian CD8αα
+
cells, which participate in the ovulation-related inflammation, may originate in the thymus. |
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ISSN: | 0022-1767 1550-6606 |