The proteomes of endometrial stromal cell-derived extracellular vesicles following a decidualizing stimulus define the cells' potential for decidualization success

被引:14
作者
Gurung, Shanti [1 ,2 ,9 ]
Greening, David W. [3 ,4 ,5 ,6 ]
Rai, Alin [3 ,5 ,6 ]
Poh, Qi Hui [3 ,4 ]
Evans, Jemma [1 ,8 ,10 ]
Salamonsen, Lois A. [1 ,7 ]
机构
[1] Hudson Inst Med Res, Ctr Reprod Hlth, Clayton, Vic, Australia
[2] Monash Univ, Dept Obstet & Gynaecol, Monash Hlth, Victoria, Australia
[3] Baker Heart & Diabet Inst, Mol Prote, 75 Commercial Rd, Melbourne, Vic 3004, Australia
[4] La Trobe Univ, La Trobe Inst Mol Sci, Dept Biochem & Genet, Bundoora, Vic, Australia
[5] Monash Univ, Cent Clin Sch, Faulty Med Nursing & Hlth Sci, Melbourne, Vic, Australia
[6] Univ Melbourne, Baker Dept Cardiometab Hlth, Melbourne, Vic, Australia
[7] Hudson Inst Med Res, Dept Mol & Translat Med, Clayton, Vic, Australia
[8] Monash Univ, Dept Physiol, Clayton, Vic, Australia
[9] Ritchie Ctr, Hudson Inst Med Res, 27-31 Wright St, Clayton, Vic 3168, Australia
[10] Nucleus Network, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
decidualized endometrial stromal cells; small extracellular vesicles; proteomics; intercellular communication; complement/coagulation cascades; RECURRENT PREGNANCY LOSS; MENSTRUAL-CYCLE; MESSENGER-RNA; EXPRESSION; SECRETOME; HEMOSTASIS; PROTEINS; HEALTH; WOMEN; IDENTIFICATION;
D O I
10.1093/molehr/gaab057
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adequate endometrial stromal cell (ESC) decidualization is vital for endometrial health. Given the importance of extracellular vesicles (EVs) in intercellular communication, we investigated how their protein landscape is reprogrammed and dysregulated during decidual response. Small EVs (sEVs) from human ESC-conditioned media at Day-2 and -14 following decidual stimuli were grouped as well- (WD) or poorly decidualized (PD) based on their prolactin secretion and subjected to mass spectrometry-based quantitative proteomics. On Day 2, in PD- versus WD-ESC-sEVs, 17 sEV- proteins were down-regulated (C5, C6; complement/coagulation cascades, and SERPING1, HRG; platelet degranulation and fibrinolysis) and 39 up-regulated (FLNA, COL1A1; focal adhesion, ENO1, PKM; glycolysis/gluconeogenesis, and RAP1B, MSN; leukocyte transendothelial migration). On Day 14, in PD- versus WD-ESC-sEVs, FLNA was down-regulated while 21 proteins were up-regulated involved in complement/coagulation cascades (C3, C6), platelet degranulation (SERPINA4, ITIH4), B-cell receptor signalling and innate immune response (immunoglobulins). Changes from Days 2 to 14 suggested a subsequent response in PD-ESC-sEVs with 89 differentially expressed proteins mostly involved in complement and coagulation cascades (C3, C6, C5), but no change in WD-ESC-sEVs ESC. Poor decidualization was also associated with loss of crucial sEV-proteins for cell adhesion and invasion (ITGA5, PFN1), glycolysis (ALDOA, PGK1) and cytoskeletal reorganization (VCL, RAC1). Overall, this study indicates varied ESC response even prior to decidualization and provides insight into sEVs-proteomes as a benchmark of well-decidualized ESC. It shows distinct variation in sEV-protein composition depending on the ESC decidual response that is critical for embryo implantation, enabling and limiting trophoblast invasion during placentation and sensing a healthy embryo.
引用
收藏
页码:1 / 17
页数:17
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