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1.
Front Endocrinol (Lausanne) ; 14: 1185147, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37501789

RESUMO

Objective: Autoimmune thyroid disease (AITD) is known to be associated with unexplained infertility in women. Although the presence of antithyroid antibodies have been speculated to be a marker of an immune imbalance that might lead to implantation failure, its underlying mechanism influencing the endometrial receptivity remains to be elucidated. In this study, we used single-cell RNA sequencing (scRNA-seq) to dissect immune microenvironment in endometrium of AITD patients during window of implantation (WOI). Methods: We collected CD45+ immune cell populations of endometrium samples of unexplained infertile women with AITD (n=3), as well as samples of AITD- controls (n=3). The cells were then processed with 10X Genomics Chromium for further analysis. Results: We characterized 28 distinct immune cell subtypes totally, and uncovered differences in the composition and gene expression patterns between AITD patients and controls. The proportions of T CD4+, cNK, ILC3, T CD8+ GZMK+, T CD8+ Cytotoxic and ILC3 CD3E - cells were increased, and CD366+ uNK1 was decreased in AITD+ patients. And the abnormal expression of GNLY and chemokines was observed in AITD patients. In addition, uNK and T CD8+ Cytotoxic cells showed lower cytotoxicity but activation of immune response. Genes enriched in cell adhesion of ILC3 and Tregs were downregulated, while the number of ILC3 and Tregs were increased. Conclusion: Immune imbalance exists in endometrium during WOI, which may impact embryo implantation.


Assuntos
Infertilidade Feminina , Doenças da Glândula Tireoide , Humanos , Feminino , Infertilidade Feminina/genética , Infertilidade Feminina/metabolismo , Transcriptoma , RNA/metabolismo , Implantação do Embrião/genética , Endométrio/metabolismo , Doenças da Glândula Tireoide/metabolismo
2.
Signal Transduct Target Ther ; 5(1): 91, 2020 06 10.
Artigo em Inglês | MEDLINE | ID: mdl-32532954

RESUMO

Cytosolic DNA is an indicator of pathogen invasion or DNA damage. The cytosolic DNA sensor cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) synthase (cGAS) detects DNA and then mediates downstream immune responses through the molecule stimulator of interferon genes (STING, also known as MITA, MPYS, ERIS and TMEM173). Recent studies focusing on the roles of the cGAS-STING pathway in evolutionary distant species have partly sketched how the mammalian cGAS-STING pathways are shaped and have revealed its evolutionarily conserved mechanism in combating pathogens. Both this pathway and pathogens have developed sophisticated strategies to counteract each other for their survival. Here, we summarise current knowledge on the interactions between the cGAS-STING pathway and pathogens from both evolutionary and mechanistic perspectives. Deeper insight into these interactions might enable us to clarify the pathogenesis of certain infectious diseases and better harness the cGAS-STING pathway for antimicrobial methods.


Assuntos
Dano ao DNA/genética , Interações Hospedeiro-Patógeno/genética , Proteínas de Membrana/genética , Nucleotidiltransferases/genética , Animais , Humanos , Imunidade Inata/genética , Mamíferos , Transdução de Sinais/genética
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