2016
DOI: 10.1111/ijlh.12599
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Myeloperoxidase in blood neutrophils during normal and abnormal menstrual cycles in women of reproductive age

Abstract: The difference in MPO between women with abnormal and normal menstrual cycles and the upregulation of MPO before ovulation suggest that neutrophils and MPO are closely related to ovulation.

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Cited by 3 publications
(3 citation statements)
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“… 25 , 26 Cluster 4 was annotated as neutrophil (NP) with high expression of CTSG, ELANE, PRTN3, AZU1, and MPO. 27 , 28 , 29 Cluster 6 was enriched expression of TLR2, ITGAM, CD163, and PECAM1, which was annotated as monocyte. 30 , 31 Cluster 8 was annotated as dendritic cell (DC) with high expression of CD1C, FCER1A, SIRPA, and ITGAX.…”
Section: Resultsmentioning
confidence: 99%
“… 25 , 26 Cluster 4 was annotated as neutrophil (NP) with high expression of CTSG, ELANE, PRTN3, AZU1, and MPO. 27 , 28 , 29 Cluster 6 was enriched expression of TLR2, ITGAM, CD163, and PECAM1, which was annotated as monocyte. 30 , 31 Cluster 8 was annotated as dendritic cell (DC) with high expression of CD1C, FCER1A, SIRPA, and ITGAX.…”
Section: Resultsmentioning
confidence: 99%
“…The cyclical expression of MPO, as well as the total absence of glandular staining in endometrial cells in anestrus, is concordant with a protein expression regulated by steroid hormones. The activity of MPO in blood neutrophils seems to be regulated by the menstrual cycle in women [54,55] and an upregulation of MPO activity by estrogens has been suggested, probably through the direct stimulation of the expression of the MPO gene [55]. In uterine tissues of rats, MPO activity was reported to increase during the follicular phase of the cycle, decrease thereafter during the luteal phase, and reach minimal values in late diestrus samples [56].…”
Section: Discussionmentioning
confidence: 99%
“…Consortium via the PRIDE partner repository 41 To verify proteomic and RNA-seq data quality, we tested expression of surface proteins used to isolate the various HSPC subpopulations as well as lineage markers with known expression in myeloid progenitors. CD34, CD38, the granulocytic marker MPO 42 and the erythroid precursor marker TFRC, a.k.a. CD71, 43 were detected at expected intensities in specific HSPC subpopulations on protein and RNA level (supplementary figure S3).…”
Section: Data Sharing Statement the Proteomics Data Have Been Deposited To The Proteomexchangementioning
confidence: 99%