Please use this identifier to cite or link to this item: https://doi.org/10.3389/fimmu.2015.00053
Title: Transcriptional factor PU.1 regulates decidual C1q expression in early pregnancy in human
Authors: Madhukaran, S.P
Kishore, U
Jamil, K
Teo, B.H.D 
Choolani, M 
Lu, J 
Keywords: complement component C1q
transcription factor PU 1
adult
Article
cell isolation
confocal microscopy
controlled study
female
first trimester pregnancy
gene expression
human
human cell
human tissue
immunofluorescence test
immunohistochemistry
normal human
polymerase chain reaction
protein expression
protein localization
reverse transcription polymerase chain reaction
stroma cell
trophoblast
Issue Date: 2015
Citation: Madhukaran, S.P, Kishore, U, Jamil, K, Teo, B.H.D, Choolani, M, Lu, J (2015). Transcriptional factor PU.1 regulates decidual C1q expression in early pregnancy in human. Frontiers in Immunology 6 (FEB) : 53. ScholarBank@NUS Repository. https://doi.org/10.3389/fimmu.2015.00053
Abstract: C1q is the first recognition subcomponent of the complement classical pathway, which in addition to being synthesized in the liver, is also expressed by macrophages and dendritic cells (DCs). Trophoblast invasion during early placentation results in accumulation of debris that triggers the complement system. Hence, both early and late components of the classical pathway are widely distributed in the placenta and decidua. In addition, C1q has recently been shown to significantly contribute to feto-maternal tolerance, trophoblast migration, and spiral artery remodeling, although the exact mechanism remains unknown. Pregnancy in mice, genetically deficient in C1q, mirrors symptoms similar to that of human preeclampsia. Thus, regulated complement activation has been proposed as an essential requirement for normal successful pregnancy. Little is known about the molecular pathways that regulate C1q expression in pregnancy. PU.1, an Ets-family transcription factor, is required for the development of hematopoietic myeloid lineage immune cells, and its expression is tissue-specific. Recently, PU.1 has been shown to regulate C1q gene expression in DCs and macrophages. Here, we have examined if PU.1 transcription factor regulates decidual C1q expression. We used immune-histochemical analysis, PCR, and immunostaining to localize and study the gene expression of PU.1 transcription factor in early human decidua. PU.1 was highly expressed at gene and protein level in early human decidual cells including trophoblast and stromal cells. Surprisingly, nuclear as well as cytoplasmic PU.1 expression was observed. Decidual cells with predominantly nuclear PU.1 expression had higher C1q expression. It is likely that nuclear and cytoplasmic PU.1 localization has a role to play in early pregnancy via regulating C1q expression in the decidua during implantation. © 2015 Madhukaran, Kishore, Jamil, Teo, Choolani and Lu.
Source Title: Frontiers in Immunology
URI: https://scholarbank.nus.edu.sg/handle/10635/174145
ISSN: 16643224
DOI: 10.3389/fimmu.2015.00053
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