Matches in SemOpenAlex for { <https://semopenalex.org/work/W2168840319> ?p ?o ?g. }
- W2168840319 endingPage "1676" @default.
- W2168840319 startingPage "1665" @default.
- W2168840319 abstract "Does NEDD8-mediated neddylation regulate human endometrial stromal proliferation and decidualization?Neddylation inhibition by a selective NEDD8-activating enzyme inhibitor, MLN4924, significantly impairs human endometrial stromal cell (HESC) proliferation and decidualization and facilitates cell senescence, via p21 accumulation.Neddylation regulates cell proliferation and tissue remodeling during embryogenesis and tumorigenesis, while human endometrial stroma undergoes sequential proliferation, differentiation, as well as dynamic tissue remodeling during each menstrual cycle.We first analyzed the expression of NEDD8 in human endometrial tissues from 50 subjects, and then explored the consequence of neddylation inhibition by MLN4924 on HESCs proliferation, decidualization and cellular senescence.We collected 50 dated human endometrial tissues from early proliferative stage to late secretory phase of the menstrual cycle and analyzed the NEDD8 expression and cellular location in human endometrium by employing quantitative real-time PCR (qRT-PCR) and immunohistochemistry staining. Similar approaches were also used to explore the mRNA and protein expression of NEDD8 in an immortalized human endometrial stromal cell line (HESC) during proliferation and decidualization (N = 6). An MTS assay was performed to evaluate the effects of neddylation inhibition by MLN4924 on HESC proliferation. Flow cytometry and BrdU incorporation assay were conducted to determine the HESC cell cycle progression in response to MLN4924 exposure during proliferation. We also analyzed F-actin distribution by phalloidin staining and decidual marker gene expression by qRT-PCR to accesses the consequence of neddylation inhibition on HESC decidualization. Immunoblotting analysis of cullin1 and p21, and SA-β-Galactosidase staining were performed to reveal the potential molecular basis for the impaired HESC proliferation, decidualization and cellular senescence. The siRNA technique was applied to knockdown p21 expression to test whether a clearance of p21 accumulation would correct the HESC defects from neddylation inhibition.We demonstrated that NEDD8 is ubiquitously expressed in human endometrium including luminal epithelium, glandular epithelium and the stromal cells during the menstrual cycle, as well as in the HESCs during proliferation and differentiation in culture. Employing multiple molecular, cellular and pharmacological approaches, we further observed that neddylation inhibition by MLN4924 significantly attenuates HESC proliferation (P-value < 0.05), impairs decidual transformation (P-value < 0.05), and facilitates cellular senescence. These abnormal HESC activities upon MLN4924 exposure were accompanied with reduced cullin1 neddylation and an aberrant accumulation of p21. While a clearance of p21 accumulation by siRNA knockdown could partially restore HESC proliferation and cellular viability, it failed to correct the decidualization defects.Since NEDD8 was also intensely expressed in the endometrial epithelium, it is interesting to further study its potential role in stroma-epithelial interactions through isolating and culturing epithelial cells. p21 siRNA knockdown experiments revealed that there are differential molecular machineries, other than p21, that are subject to neddylation regulation during HESC proliferation compared with differentiation. This alternative mechanism warrants further investigation in future.Our findings add novel evidence showing, for what we believe the first time, that NEDD8-mediated neddylation is required for normal human endometrial functions, which raises the possibility of approaching the neddylation system for diagnosis and treatment of infertility in women.This work was supported in parts by the National Basic Research Program of China (2011CB944400 to H.W.) and the National Natural Science Foundation (81130009, 81330017 to H.W., 81170575 to S.Q. and 31471106 to S.Z.). The author declares that there is no conflict of interest." @default.
- W2168840319 created "2016-06-24" @default.
- W2168840319 creator A5002744113 @default.
- W2168840319 creator A5010441190 @default.
- W2168840319 creator A5017606280 @default.
- W2168840319 creator A5024598893 @default.
- W2168840319 creator A5027496356 @default.
- W2168840319 creator A5055941149 @default.
- W2168840319 creator A5056484501 @default.
- W2168840319 creator A5059234351 @default.
- W2168840319 creator A5062395667 @default.
- W2168840319 creator A5077055427 @default.
- W2168840319 date "2015-05-23" @default.
- W2168840319 modified "2023-10-14" @default.
- W2168840319 title "NEDD8-mediated neddylation is required for human endometrial stromal proliferation and decidualization" @default.
- W2168840319 cites W1504206591 @default.
- W2168840319 cites W1539642496 @default.
- W2168840319 cites W1970817319 @default.
- W2168840319 cites W1970924670 @default.
- W2168840319 cites W1973425911 @default.
- W2168840319 cites W1982461390 @default.
- W2168840319 cites W1982481909 @default.
- W2168840319 cites W1993866784 @default.
- W2168840319 cites W1997096605 @default.
- W2168840319 cites W2001827754 @default.
- W2168840319 cites W2006494078 @default.
- W2168840319 cites W2014114945 @default.
- W2168840319 cites W2033877970 @default.
- W2168840319 cites W2035434033 @default.
- W2168840319 cites W2036806530 @default.
- W2168840319 cites W2041063291 @default.
- W2168840319 cites W2046256501 @default.
- W2168840319 cites W2053220683 @default.
- W2168840319 cites W2062687768 @default.
- W2168840319 cites W2062980622 @default.
- W2168840319 cites W2066745745 @default.
- W2168840319 cites W2068413946 @default.
- W2168840319 cites W2076194625 @default.
- W2168840319 cites W2079185705 @default.
- W2168840319 cites W2080939719 @default.
- W2168840319 cites W2091124764 @default.
- W2168840319 cites W2095222072 @default.
- W2168840319 cites W2097871251 @default.
- W2168840319 cites W2108004598 @default.
- W2168840319 cites W2109801386 @default.
- W2168840319 cites W2119975890 @default.
- W2168840319 cites W2127365820 @default.
- W2168840319 cites W2130463115 @default.
- W2168840319 cites W2139290675 @default.
- W2168840319 cites W2140219059 @default.
- W2168840319 cites W2140252926 @default.
- W2168840319 cites W2141957886 @default.
- W2168840319 cites W2153074997 @default.
- W2168840319 cites W2154416379 @default.
- W2168840319 cites W2157330515 @default.
- W2168840319 cites W2164576139 @default.
- W2168840319 cites W2166072653 @default.
- W2168840319 cites W2169179975 @default.
- W2168840319 cites W2181935758 @default.
- W2168840319 cites W2327334027 @default.
- W2168840319 cites W2345696364 @default.
- W2168840319 cites W2504155943 @default.
- W2168840319 doi "https://doi.org/10.1093/humrep/dev117" @default.
- W2168840319 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26003431" @default.
- W2168840319 hasPublicationYear "2015" @default.
- W2168840319 type Work @default.
- W2168840319 sameAs 2168840319 @default.
- W2168840319 citedByCount "30" @default.
- W2168840319 countsByYear W21688403192016 @default.
- W2168840319 countsByYear W21688403192017 @default.
- W2168840319 countsByYear W21688403192018 @default.
- W2168840319 countsByYear W21688403192019 @default.
- W2168840319 countsByYear W21688403192020 @default.
- W2168840319 countsByYear W21688403192021 @default.
- W2168840319 countsByYear W21688403192022 @default.
- W2168840319 countsByYear W21688403192023 @default.
- W2168840319 crossrefType "journal-article" @default.
- W2168840319 hasAuthorship W2168840319A5002744113 @default.
- W2168840319 hasAuthorship W2168840319A5010441190 @default.
- W2168840319 hasAuthorship W2168840319A5017606280 @default.
- W2168840319 hasAuthorship W2168840319A5024598893 @default.
- W2168840319 hasAuthorship W2168840319A5027496356 @default.
- W2168840319 hasAuthorship W2168840319A5055941149 @default.
- W2168840319 hasAuthorship W2168840319A5056484501 @default.
- W2168840319 hasAuthorship W2168840319A5059234351 @default.
- W2168840319 hasAuthorship W2168840319A5062395667 @default.
- W2168840319 hasAuthorship W2168840319A5077055427 @default.
- W2168840319 hasBestOaLocation W21688403191 @default.
- W2168840319 hasConcept C104317684 @default.
- W2168840319 hasConcept C126322002 @default.
- W2168840319 hasConcept C134459356 @default.
- W2168840319 hasConcept C1491633281 @default.
- W2168840319 hasConcept C16930146 @default.
- W2168840319 hasConcept C172680121 @default.
- W2168840319 hasConcept C25602115 @default.
- W2168840319 hasConcept C2776953305 @default.
- W2168840319 hasConcept C2778316770 @default.
- W2168840319 hasConcept C2779231659 @default.