Circulating immunoglobulin A‐ and immunoglobulin G‐secreting hybridoma cells in peripheral blood preferably migrate to female genital tracts. The role of sex hormones

Male Mice, Inbred BALB C Sex Characteristics Hybridomas Estradiol Cell Culture Techniques Genitalia, Female Genitalia, Male Immunoglobulin A 3. Good health Mice 03 medical and health sciences 0302 clinical medicine Cell Movement Immunoglobulin G Antigens, Surface Animals Female Testosterone Antibody-Producing Cells Gonadal Steroid Hormones Progesterone
DOI: 10.1046/j.1365-2567.2002.01433.x Publication Date: 2003-03-12T02:31:27Z
ABSTRACT
SummaryAntigen‐specific circulating immunoglobulin‐secreting cells (ISC) migrate to various secondary and tertiary lymphoid tissues. To understand the migration of the cells into the genital tract and its regulation by sex hormones, spleen‐derived SG2 hybridoma cells secreting immunoglobulin G2b (IgG2b) and Peyer's patch‐derived PA4 hybridoma cells secreting polymer IgA were labelled with 3H‐TdR, and intravenously injected into syngeneic mice of both sexes. Using flow cytometry, surface molecular markers of plasma cells, CD38 and CD138, and adhesion molecules, CD49d, CD162, and CD11a were found to be positive in SG2 and PA4 cells, but CD62L, α4β7 and CD44 were not expressed on these cells. The relative distribution indexes (RDIs) of the cells in genital tract and other tissues were measured. The means of RDIs of SG2 and PA4 cells in female genital tissues were 6·5 and 4·5 times as many as the means in male genital tissues, respectively. The treatment of ovariectomized mice with β‐oestradiol significantly increased the RDIs of PA4 cells in cervix and vagina, but decreased the RDIs of SG2 cells in vagina, horn of uterus, uterus and rectum (P<0·05). Progesterone treatment increased the RDIs of PA4 cells in vagina and rectum (P<0·05). The treatment with testosterone significantly increased the RDIs of SG2 and PA4 cells in epididymis and accessory sex glands (P<0·05). These results demonstrate that the female genital tract is the preferable site for the migration of circulating hybridoma cells to the male genital tract, and sex hormones play an important role in regulation of the migration of circulating ISC to genital tracts.
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