33 research outputs found

    Elevated human placental heat shock protein 5 is associated with spontaneous preterm birth

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    Background: Specific heat shock proteins are associated with pregnancy complications, including spontaneous preterm birth (SPTB). Placental proteomics and whole exome sequencing recently suggested an association between heat shock protein HSPA5 and uncomplicated SPTB. In the present study, we investigated the localization of and possible roles for HSPA5 in SPTB. Methods: Western blot was performed to validate the result from the previously published proteomic analysis. We used qPCR to assess mRNA expression of genes and immunohistochemistry and immunoelectron microscopy to examine localization of HSPA5 in placental tissue. We silenced the HSPA5 gene in the HTR8/SVneo human trophoblast cell line to investigate possible functions of HSPA5. Results: HSPA5 was upregulated in placentas from SPTBs compared to spontaneous term births. We did not observe upregulation of HSPA5 mRNA in placental samples. The protein was localized in placental trophoblast in both spontaneous preterm and term placentas. Gene silencing of HSPA5 in human trophoblast cell culture affected the inflammatory response and decreased the expression of several proinflammatory genes. Conclusions: We suggest that upregulation of HSPA5 in the placenta is associated with spontaneous preterm labor. HSPA5 may promote the inflammatory response and alter the anti-inflammatory state of the placenta which could eventually lead to premature labor. Impact: We validated upregulation of HSPA5 in placentas from spontaneous preterm birth. HSPA5 was not upregulated at transcriptional level which suggests that it may be regulated post-translationally.Silencing HSPA5 in a human trophoblast–derived cell line suggested that HSPA5 promotes expression of proinflammatory cytokines. The emerging inflammation could lead to spontaneous preterm labor.Identifying inflammatory pathways and factors associated with spontaneous preterm birth increases knowledge of the molecular mechanisms of premature labor. This could provide cues to predict imminent premature labor and lead to information about how to safely maintain pregnancies.publishedVersionPeer reviewe

    Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth

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    Background: Preterm birth is defined as live birth before 37 completed weeks of pregnancy, and it is a major problem worldwide. The molecular mechanisms that lead to onset of spontaneous preterm birth are incompletely understood. Prediction and evaluation of the risk of preterm birth is challenging as there is a lack of accurate biomarkers. In this study, our aim was to identify placental proteins that associate with spontaneous preterm birth. Methods: We analyzed the proteomes from placentas to identify proteins that associate with both gestational age and spontaneous labor. Next, rare and potentially damaging gene variants of the identified protein candidates were sought for from our whole exome sequencing data. Further experiments we performed on placental samples and placenta-associated cells to explore the location and function of the spontaneous preterm labor-associated proteins in placentas. Results: Exome sequencing data revealed rare damaging variants in SERPINA1 in families with recurrent spontaneous preterm deliveries. Protein and mRNA levels of alpha-1 antitrypsin/SERPINA1 from the maternal side of the placenta were downregulated in spontaneous preterm births. Alpha-1 antitrypsin was expressed by villous trophoblasts in the placenta, and immunoelectron microscopy showed localization in decidual fibrinoid deposits in association with specific extracellular proteins. siRNA knockdown in trophoblast-derived HTR8/SVneo cells revealed that SERPINA1 had a marked effect on regulation of the actin cytoskeleton pathway, Slit–Robo signaling, and extracellular matrix organization. Conclusions: Alpha-1 antitrypsin is a protease inhibitor. We propose that loss of the protease inhibition effects of alpha-1 antitrypsin renders structures critical to maintaining pregnancy susceptible to proteases and inflammatory activation. This may lead to spontaneous premature birth.publishedVersionPeer reviewe

    Expression of CPPED1 in human trophoblasts is associated with timing of term birth

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    Understanding of timing of human parturition is incomplete. Therefore, we carried out proteomic analyses of full-term placentas from uncomplicated pregnancies to identify protein signatures associated with the onset of spontaneous delivery. We found quantitative associations of 10 proteins with spontaneous term birth, evident either in the basal or in the chorionic plates or in both. Additional 18 proteins were associated according to the location within placenta indicating local variations in protein amounts. Calcineurin-like phosphoesterase domain-containing 1 (CPPED1), a phosphatase previously suggested dephosphorylating AKT1/PKB, was one of the identified proteins. qRT-PCR revealed the mRNA level of CPPED1 was higher in elective caesarean deliveries than in spontaneous births, while immunohistochemistry showed CPPED1 in cytotrophoblasts, syncytiotrophoblasts and extravillous trophoblasts. Noteworthy, phosphorylation status of AKT1 did not differ between placentas from elective caesarean and spontaneous deliveries. Additionally, analyses of samples from infants indicated that single-nucleotide polymorphisms rs11643593 and rs8048866 of CPPED1 were associated with duration of term pregnancy. Finally, post-transcriptional silencing of CPPED1 in cultured HTR8/SVneo cells by siRNAs affected gene expression in pathways associated with inflammation and blood vessel development. We postulate that functions regulated by CPPED1 in trophoblasts at choriodecidual interphase have a role in the induction of term labour, but it may be independent of AKT1

    Differences in Ultrasonic Indications:Thermal Fatigue Cracks and EDM Notches

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    Differences in Ultrasonic Indications:Thermal Fatigue Cracks and EDM Notches

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    Ferric and Cupric Chloride Leaching of Valuable Metals from Process Residues

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    | openaire: EC/H2020/721385/EU//SOCRATESThe object of the current study was to compare the extraction yields of various valuable metals from process residues by ferric and cupric chloride leaching as an alternative to cyanidation. Flotation tailings, with low amount of gold, copper, nickel, cobalt and zinc were used as a raw material. In the chloride leaching experiments, the effect of the oxidant type and concentration ([Fe3+] and [Cu2+] from 10 to 50 g/L), was investigated on the metals extraction. At the same time, pH (1 and 1.8), temperature (95 °C), solid/liquid ratio (25 %), oxygen feed rate (1200 mL/min), leaching time (24 h), and stirring rate (950 rpm) were kept constant. Additionally, the reference leaching experiment with sodium cyanide (NaCN) at 22 °C, pH = 11, solid/liquid ratio of 25 %, air feed rate 500 ml/min, stirring rate 400 rpm and 24 hours of leaching time was run to benchmark leaching efficiencies of cyanide-free processes. The results showed that the maximum gold extraction was observed with cyanidation (78 %) and followed byferric and cupric chloride leaching. For copper, the extractions were higher in chloride leaching (75 – 100 %) whereas cyanide could dissolve 50 % of copper. Extraction of nickel and zinc were slightly higher in ferric chloride leaching compared to cupric chloride leaching, but cobalt extraction was similar in both chloride leaching methods. However, extraction of these metals was insignificant in cyanide leaching. With these results, it seems that chloride leaching with the presence of cupric and ferric oxidants can be used as an alternative cyanide-free method for extraction of metals from process residues.Peer reviewe
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