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The Placental Immunomodulatory Cytokine Regeneration and Tolerance Factor is also Expressed by Both Human Cycling and Early Pregnant Endometrium
Author(s) -
Lattuada Debora,
Mangioni Silvia,
Viganò Paola,
Ntrivalas Evangelos I.,
Rossi Margherita,
Palotti Francesco,
Carinelli Silvestro,
Beaman Kenneth D.,
Di Blasio Anna M.
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.1600-0897.2004.00210.x
Subject(s) - endometrium , stromal cell , biology , decidua , cytokine , endocrinology , andrology , medicine , placenta , tumor necrosis factor alpha , immunology , fetus , pregnancy , cancer research , genetics
Problem: Regeneration and tolerance factor (RTF) has been recently suggested to contribute to the control of fetal‐ablating immunity at the maternal–fetal interface through the induction of T helper 2 (Th2)‐dominated response. The protein consists of a membrane‐associated domain and an extracellular portion which is proteolitically cleaved to yield a soluble peptide. In humans, it has been shown to be expressed by invading cytotrophoblasts and decidual lymphoid cells, to be increased on peripheral blood B lymphocytes during a normal gestation and on circulating natural killer cells during unsuccessful pregnancies. However, the expression of RTF in other cell types and, specifically, in non‐hematopoietic maternal cells of the human uterus has not been characterized in detail. Thus, we have specifically studied the expression and modulation of the cytokine in human endometrium obtained in different phases of the cycle and in early pregnancy. Methods: The 20 kDa extracellular domain of RTF has been localized by immunohistochemical method and Western blot analysis. Levels of RTF messenger RNA (mRNA) in basal and stimulated conditions have been evaluated by semiquantitative reverse transcription‐polymerase chain reaction. Results: The extracellular domain of RTF could be detected in both the glandular epithelium and stroma with diffuse distribution in both cycling endometrium and first trimester decidua. Both cycling and pregnant endometrium expressed the gene for RTF but mRNA levels resulted significantly increased in secretory phase‐endometrial stromal cells when compared to proliferative phase samples. Inflammatory cytokines, interleukin‐1 β and tumour necrosis factor α were able to directly increase endometrial RTF mRNA expression. Conclusion: These results indicate that RTF is constitutively expressed at endometrial and decidual level and its up‐regulation during the secretory phase of the cycle may be relevant in mediating some immune‐related aspects of uterine physiology.