EXPRESSION AND REGULATION OF HISTIDINE DECARBOXYLASE mRNA EXPRESSION IN THE UTERUS DURING PREGNANCY IN THE MOUSE

• Published in: Cytokine (Philadelphia, Pa.) Vol. 12; no. 6; pp. 622 - 629
• Main Authors: Wood, Gary W, Hausmann, Elda H.S, Choudhuri, Rajani, Dileepan, Kottarappat N
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.06.2000
• Subjects: Animals; Chemokine CCL2 - genetics; Chemokine CCL5 - genetics; Cytokines - genetics; Embryo Implantation; Female; Gene Expression Regulation; Gene Expression Regulation, Enzymologic; Histidine Decarboxylase - genetics; histidine decarboxylase/histamine/IL-1/implantation/MCP-1/pregnancy/pseudopregnancy/RANTES/uterus; Interleukin-1 - genetics; Male; Mice; Mice, Inbred Strains; Pregnancy; Pregnancy, Animal - immunology; Pregnancy, Animal - physiology; RNA, Messenger - genetics; T-Lymphocytes - immunology; Transcription, Genetic; Uterus - enzymology; Uterus - immunology; histidine decarboxylase/histamine/IL-1/implantation/MCP-1/pregnancy/pseudopregnancy/RANTES/uterus
• ISSN: 1043-4666; 1096-0023
• DOI: 10.1006/cyto.2000.0667

It has been hypothesized that hormonally regulated histamine production plays a role in preparation of the uterus for implantation. Histidine decarboxylase (HDC) is the rate-limiting enzyme for histamine production. The current study was designed to determine intrauterine expression of HDC mRNA expression during pregnancy in the mouse. High levels of HDC mRNA expression were observed in the preimplantation mouse uterus with peak expression occurring on day 4. High levels of HDC mRNA expression were also detected in the post-implantation uterus. In an effort to determine whether HDC mRNA is regulated by pro-inflammatory cytokines, the HDC mRNA pattern was compared to intrauterine expression of mRNA's for interleukin-1α (IL-1α), IL-1β, macrophage chemotactic protein-1 (MCP-1) and RANTES (regulated on activation, normal T expressed and secreted) during the peri-implantation period. IL-1β, MCP-1 and RANTES mRNA levels were increased in the uterus on days 1–2 and on days 4–5. Increased expression of IL-1α mRNA was observed on days 1–2 and days 5–7. There was no clear relationship between HDC mRNA expression and cytokine/chemokine mRNA expression. Progesterone-stimulated intrauterine expression of HDC mRNA. Intrauterine cytokine/chemokine mRNA was also hormonally regulated. This data allowed the possibility that one or more of these pro-inflammatory cytokines could be involved in regulating intrauterine HDC mRNA production. Recombinant IL-1α, IL-1β, MCP-1 and RANTES all failed to induce HDC mRNA expression in the preimplantation uterus in a mouse pseudopregnancy model. At the same time, IL-1β induced the expression of mRNA for each of the four cytokines/chemokines. Despite the fact that these were also produced in the uterus during pregnancy and were hormonally regulated, none of these cytokines induced intrauterine HDC mRNA expression. The data suggest that progesterone is involved in the regulation of HDC mRNA expression in the preimplantation uterus, but IL-1α/β, MCP-1 and RANTES, which have been reported to regulate histamine synthesis during inflammatory processes, do not appear to play a role.