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The Immune Environment in Human Endometrium during the Window of Implantation
Author(s) -
Lobo Shalini C.,
Huang S.T. Joseph,
Germeyer Ariane,
Dosiou Chrysoula,
Vo Kim Chi,
Tulac Suzana,
Nayak Nihar R.,
Giudice Linda C.
Publication year - 2004
Publication title -
american journal of reproductive immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 97
eISSN - 1600-0897
pISSN - 1046-7408
DOI - 10.1111/j.1600-0897.2004.00217.x
Subject(s) - endometrium , downregulation and upregulation , biology , immune system , microarray analysis techniques , andrology , immunology , endocrinology , medicine , gene expression , gene , genetics
Problem: Changes in the immune environment in the endometrium are believed to be important for successful implantation and maintenance of pregnancy. We have previously investigated global gene profiling in human endometrium during the window of implantation by oligonucleotide microarray technology, and analysis of these data underscore the regulation of a group of immune‐related genes. The present study was therefore conducted to examine the pattern of expression and regulation of these genes including decay accelerating factor (DAF), indoleamine 2,3 dioxygenase (IDO), interleukin‐15 (IL‐15), IL‐15 receptor alpha subunit (IL‐15R α ), interferon regulatory factor‐1 (IRF‐1), lymphotactin (Lpn), natural killer‐associated transcript 2 (NKAT2) and NKG5 in secretory and proliferative human endometrium. Method of Study: Endometrial biopsies were obtained from normally cycling women in the late proliferative and mid‐secretory phase of the menstrual cycle. Semi‐quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) and Northern blot analysis were used to determine the expression and regulation of these genes in secretory and proliferative human endometrium. Cellular localization of NKG5, Lpn and IDO by in situ hybridization in secretory‐phase endometrium was also examined. Results: Semi‐quantitative RT‐PCR and Northern blot results demonstrate that there is a coordinated upregulation of this group of genes during the window of implantation. Conclusions: We demonstrate the upregulation of immune‐related genes IL‐15R α , Lpn and NKG5 in secretory versus proliferative human endometrium. We also demonstrate a similar upregulation in secretory endometrium of other immune‐related genes, viz, DAF, IDO, IL‐15, IRF‐1 and NKAT2. The functions of these genes include stimulation of proliferation of uterine natural killer (uNK) cells, inhibition of cytolytic activity of uNK cells, inhibition of cell growth of T cells and other pathogens and inhibition of the classical complement pathway. Upregulation of these immune‐related genes in the window of implantation suggests their role during the process of implantation and in immune tolerance of the implanting conceptus.