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  • 1
    In: Immunology & Cell Biology, Wiley, Vol. 96, No. 7 ( 2018-08), p. 742-758
    Abstract: Human blood monocytes are subclassified as classical, intermediate and nonclassical. In this study, it was shown that conventionally defined human intermediate monocytes can be divided into two distinct subpopulations with mid‐ and high‐level surface expression of HLA ‐ DR (referred to as DR mid and DR hi intermediate monocytes). These IM subpopulations were phenotypically and functionally characterized in healthy adult blood by flow cytometry, migration assays and lipoprotein uptake assays. Their absolute numbers and proportions were then compared in blood samples from obese and nonobese adults. DR mid and DR hi intermediate monocytes differentially expressed several proteins including CD 62L, CD 11a, CX 3 CR 1 and CCR 2. Overall, the DR mid intermediate monocytes surface profile more closely resembled that of classical monocytes while DR hi intermediate monocytes were more similar to nonclassical. However, in contrast to classical monocytes, DR mid intermediate monocytes migrated weakly to CCL 2, had reduced intracellular calcium flux following CCR 2 ligation and favored adherence to TNF α‐activated endothelium over transmigration. In lipid uptake assays, DR mid intermediate monocytes demonstrated greater internalization of oxidized and acetylated low‐density lipoprotein than DR hi intermediate monocytes. In obese compared to nonobese adults, proportions and absolute numbers of DR mid , but not DR hi intermediate monocytes, were increased in blood. The results are consistent with phenotypic and functional heterogeneity within the intermediate monocytes subset that may be of specific relevance to lipoprotein scavenging and metabolic health.
    Type of Medium: Online Resource
    ISSN: 0818-9641 , 1440-1711
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2011707-3
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2012
    In:  FEBS Open Bio Vol. 2, No. 1 ( 2012-01), p. 313-317
    In: FEBS Open Bio, Wiley, Vol. 2, No. 1 ( 2012-01), p. 313-317
    Abstract: Under normal conditions histone H2AX is constitutively phosphorylated on tyrosine (Y) 142 by Williams–Beuren syndrome transcription factor kinase (WSTF). Following DNA double strand breaks (DSB), Y142 is de‐phosphorylated and serine (S) 139 is phosphorylated. Here we explored DSB‐dependent cross talk between H2AX residues S139 and Y142. H2axY142A mutation resulted in increased sensitivity to ionising radiation (IR), compared to H2axS139A . Interestingly, co‐mutation of S139A and Y142A rescued IR sensitivity. The DSB response proteins 53Bp1 and Rad51 were recruited to IR‐induced foci (IRIF) in H2axS139A , H2axY142A and H2axS139A / Y142A cells. Our results suggest that H2axY142A IR sensitivity is dependent upon the C‐terminal residue, S139.
    Type of Medium: Online Resource
    ISSN: 2211-5463 , 2211-5463
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 2651702-4
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