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  1. Article ; Online: Accurate quantification of bacterial abundance in metagenomic DNAs accounting for variable DNA integrity levels.

    Manzari, Caterina / Oranger, Annarita / Fosso, Bruno / Piancone, Elisabetta / Pesole, Graziano / D'Erchia, Anna Maria

    Microbial genomics

    2020  Volume 6, Issue 10

    Abstract: The quantification of the total microbial content in metagenomic samples is critical for investigating the interplay between the microbiome and its host, as well as for assessing the accuracy and precision of the relative microbial composition which can ... ...

    Abstract The quantification of the total microbial content in metagenomic samples is critical for investigating the interplay between the microbiome and its host, as well as for assessing the accuracy and precision of the relative microbial composition which can be strongly biased in low microbial biomass samples. In the present study, we demonstrate that digital droplet PCR (ddPCR) can provide accurate quantification of the total copy number of the 16S rRNA gene, the gene usually exploited for assessing total bacterial abundance in metagenomic DNA samples. Notably, using DNA templates with different integrity levels, as measured by the DNA integrity number (DIN), we demonstrated that 16S rRNA copy number quantification is strongly affected by DNA quality and determined a precise correlation between quantification underestimation and DNA degradation levels. Therefore, we propose an input DNA mass correction, according to the observed DIN value, which could prevent inaccurate quantification of 16S copy number in degraded metagenomic DNAs. Our results highlight that a preliminary evaluation of the metagenomic DNA integrity should be considered before performing metagenomic analyses of different samples, both for the assessment of the reliability of observed differential abundances in different conditions and to obtain significant functional insights.
    MeSH term(s) Algorithms ; Bacteria/classification ; Bacteria/genetics ; DNA, Bacterial/genetics ; Metagenome/genetics ; Microbiota/genetics ; RNA, Ribosomal, 16S/genetics
    Chemical Substances DNA, Bacterial ; RNA, Ribosomal, 16S
    Language English
    Publishing date 2020-08-04
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2835258-0
    ISSN 2057-5858 ; 2057-5858
    ISSN (online) 2057-5858
    ISSN 2057-5858
    DOI 10.1099/mgen.0.000417
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Natural and after colon washing fecal samples: the two sides of the coin for investigating the human gut microbiome.

    Piancone, Elisabetta / Fosso, Bruno / Marzano, Marinella / De Robertis, Mariangela / Notario, Elisabetta / Oranger, Annarita / Manzari, Caterina / Bruno, Silvia / Visci, Grazia / Defazio, Giuseppe / D'Erchia, Anna Maria / Filomena, Ermes / Maio, Dominga / Minelli, Martina / Vergallo, Ilaria / Minelli, Mauro / Pesole, Graziano

    Scientific reports

    2022  Volume 12, Issue 1, Page(s) 17909

    Abstract: To date several studies address the important role of gut microbiome and its interplay with the human host in the health and disease status. However, the selection of a universal sampling matrix representative of the microbial biodiversity associated ... ...

    Abstract To date several studies address the important role of gut microbiome and its interplay with the human host in the health and disease status. However, the selection of a universal sampling matrix representative of the microbial biodiversity associated with the gastrointestinal (GI) tract, is still challenging. Here we present a study in which, through a deep metabarcoding analysis of the 16S rRNA gene, we compared two sampling matrices, feces (F) and colon washing feces (CWF), in order to evaluate their relative effectiveness and accuracy in representing the complexity of the human gut microbiome. A cohort of 30 volunteers was recruited and paired F and CWF samples were collected from each subject. Alpha diversity analysis confirmed a slightly higher biodiversity of CWF compared to F matched samples. Likewise, beta diversity analysis proved that paired F and CWF microbiomes were quite similar in the same individual, but remarkable inter-individual variability occurred among the microbiomes of all participants. Taxonomic analysis in matched samples was carried out to investigate the intra and inter individual/s variability. Firmicutes, Bacteroidota, Proteobacteria and Actinobacteriota were the main phyla in both F and CWF samples. At genus level, Bacteirodetes was the most abundant in F and CWF samples, followed by Faecalibacterium, Blautia and Escherichia-Shigella. Our study highlights an inter-individual variability greater than intra-individual variability for paired F and CWF samples. Indeed, an overall higher similarity was observed across matched F and CWF samples, suggesting, as expected, a remarkable overlap between the microbiomes inferred using the matched F and CWF samples. Notably, absolute quantification of total 16S rDNA by droplet digital PCR (ddPCR) revealed comparable overall microbial load between paired F and CWF samples. We report here the first comparative study on fecal and colon washing fecal samples for investigating the human gut microbiome and show that both types of samples may be used equally for the study of the gut microbiome. The presented results suggest that the combined use of both types of sampling matrices could represent a suitable choice to obtain a more complete overview of the human gut microbiota for addressing different biological and clinical questions.
    MeSH term(s) Humans ; Gastrointestinal Microbiome/genetics ; RNA, Ribosomal, 16S/genetics ; Feces/microbiology ; Microbiota ; DNA, Ribosomal ; Colon
    Chemical Substances RNA, Ribosomal, 16S ; DNA, Ribosomal
    Language English
    Publishing date 2022-10-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-022-20888-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Accurate detection and quantification of SARS-CoV-2 genomic and subgenomic mRNAs by ddPCR and meta-transcriptomics analysis.

    Oranger, Annarita / Manzari, Caterina / Chiara, Matteo / Notario, Elisabetta / Fosso, Bruno / Parisi, Antonio / Bianco, Angelica / Iacobellis, Michela / d'Avenia, Morena / D'Erchia, Anna Maria / Pesole, Graziano

    Communications biology

    2021  Volume 4, Issue 1, Page(s) 1215

    Abstract: SARS-CoV-2 replication requires the synthesis of a set of structural proteins expressed through discontinuous transcription of ten subgenomic mRNAs (sgmRNAs). Here, we have fine-tuned droplet digital PCR (ddPCR) assays to accurately detect and quantify ... ...

    Abstract SARS-CoV-2 replication requires the synthesis of a set of structural proteins expressed through discontinuous transcription of ten subgenomic mRNAs (sgmRNAs). Here, we have fine-tuned droplet digital PCR (ddPCR) assays to accurately detect and quantify SARS-CoV-2 genomic ORF1ab and sgmRNAs for the nucleocapsid (N) and spike (S) proteins. We analyzed 166 RNA samples from anonymized SARS-CoV-2 positive subjects and we observed a recurrent and characteristic pattern of sgmRNAs expression in relation to the total viral RNA content. Additionally, expression profiles of sgmRNAs, as determined by meta-transcriptomics sequencing of a subset of 110 RNA samples, were highly correlated with those obtained by ddPCR. By providing a comprehensive and dynamic snapshot of the levels of SARS-CoV-2 sgmRNAs in infected individuals, our results may contribute a better understanding of the dynamics of transcription and expression of the genome of SARS-CoV-2 and facilitate the development of more accurate molecular diagnostic tools for the stratification of COVID-19 patients.
    MeSH term(s) COVID-19/genetics ; COVID-19/metabolism ; COVID-19 Nucleic Acid Testing/methods ; Computational Biology ; Coronavirus Nucleocapsid Proteins ; Humans ; Limit of Detection ; Open Reading Frames ; Phosphoproteins ; Polymerase Chain Reaction/methods ; RNA, Messenger/metabolism ; RNA, Viral/metabolism ; Real-Time Polymerase Chain Reaction ; Reproducibility of Results ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Transcriptome
    Chemical Substances Coronavirus Nucleocapsid Proteins ; Phosphoproteins ; RNA, Messenger ; RNA, Viral ; Spike Glycoprotein, Coronavirus ; nucleocapsid phosphoprotein, SARS-CoV-2 ; spike protein, SARS-CoV-2
    Language English
    Publishing date 2021-10-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2399-3642
    ISSN (online) 2399-3642
    DOI 10.1038/s42003-021-02748-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The pathological role of the ubiquitination pathway in diabetic nephropathy.

    Pontrelli, Paola / Oranger, Annarita / Barozzino, Mariagrazia / Conserva, Francesca / Papale, Massimo / Gesualdo, Loreto

    Minerva medica

    2017  

    Abstract: Diabetic nephropathy (DN) is a chronic complication of type 2 diabetes and is the most frequent form of chronic kidney disease that can lead to end-stage renal disease. Different pathways, involved in oxidative stress, inflammation, fibrosis and cell ... ...

    Abstract Diabetic nephropathy (DN) is a chronic complication of type 2 diabetes and is the most frequent form of chronic kidney disease that can lead to end-stage renal disease. Different pathways, involved in oxidative stress, inflammation, fibrosis and cell death, are responsible for the pathogenesis of DN and regulate the progression of the disease. Ubiquitination is a fundamental pathway in intracellular signaling whose role is emerging in the regulation of molecular processes responsible for several human diseases. Among the conventional ubiquitination pathway, leading to proteasomal degradation of proteins, also non-conventional ubiquitination plays an important role in the regulation of intracellular signaling. Several proteasome inhibitors have been developed and tested both in humans and in animal models and show potential as promising therapeutic approaches. In this review, we focused our attention on the role of ubiquitination pathway in the principal processes involved in the pathogenesis and progression of DN.
    Language English
    Publishing date 2017-10-03
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 123586-2
    ISSN 1827-1669 ; 0026-4806
    ISSN (online) 1827-1669
    ISSN 0026-4806
    DOI 10.23736/S0026-4806.17.05419-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Accurate detection and quantification of SARS-CoV-2 genomic and subgenomic mRNAs by ddPCR and meta-transcriptomics analysis

    Annarita Oranger / Caterina Manzari / Matteo Chiara / Elisabetta Notario / Bruno Fosso / Antonio Parisi / Angelica Bianco / Michela Iacobellis / Morena d’Avenia / Anna Maria D’Erchia / Graziano Pesole

    Communications Biology, Vol 4, Iss 1, Pp 1-

    2021  Volume 10

    Abstract: Oranger et al use digital droplet PCR to develop an assay that provides a dynamic snapshot ...

    Abstract Oranger et al use digital droplet PCR to develop an assay that provides a dynamic snapshot of the levels of SARS-CoV-2 sub-genomic messanger RNA in infected individuals. This has the potential to improve diagnostic accuracy for COVID-19
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2021-10-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Natural and after colon washing fecal samples

    Elisabetta Piancone / Bruno Fosso / Marinella Marzano / Mariangela De Robertis / Elisabetta Notario / Annarita Oranger / Caterina Manzari / Silvia Bruno / Grazia Visci / Giuseppe Defazio / Anna Maria D’Erchia / Ermes Filomena / Dominga Maio / Martina Minelli / Ilaria Vergallo / Mauro Minelli / Graziano Pesole

    Scientific Reports, Vol 12, Iss 1, Pp 1-

    the two sides of the coin for investigating the human gut microbiome

    2022  Volume 14

    Abstract: Abstract To date several studies address the important role of gut microbiome and its interplay with the human host in the health and disease status. However, the selection of a universal sampling matrix representative of the microbial biodiversity ... ...

    Abstract Abstract To date several studies address the important role of gut microbiome and its interplay with the human host in the health and disease status. However, the selection of a universal sampling matrix representative of the microbial biodiversity associated with the gastrointestinal (GI) tract, is still challenging. Here we present a study in which, through a deep metabarcoding analysis of the 16S rRNA gene, we compared two sampling matrices, feces (F) and colon washing feces (CWF), in order to evaluate their relative effectiveness and accuracy in representing the complexity of the human gut microbiome. A cohort of 30 volunteers was recruited and paired F and CWF samples were collected from each subject. Alpha diversity analysis confirmed a slightly higher biodiversity of CWF compared to F matched samples. Likewise, beta diversity analysis proved that paired F and CWF microbiomes were quite similar in the same individual, but remarkable inter-individual variability occurred among the microbiomes of all participants. Taxonomic analysis in matched samples was carried out to investigate the intra and inter individual/s variability. Firmicutes, Bacteroidota, Proteobacteria and Actinobacteriota were the main phyla in both F and CWF samples. At genus level, Bacteirodetes was the most abundant in F and CWF samples, followed by Faecalibacterium, Blautia and Escherichia-Shigella. Our study highlights an inter-individual variability greater than intra-individual variability for paired F and CWF samples. Indeed, an overall higher similarity was observed across matched F and CWF samples, suggesting, as expected, a remarkable overlap between the microbiomes inferred using the matched F and CWF samples. Notably, absolute quantification of total 16S rDNA by droplet digital PCR (ddPCR) revealed comparable overall microbial load between paired F and CWF samples. We report here the first comparative study on fecal and colon washing fecal samples for investigating the human gut microbiome and show that both types of samples may ...
    Keywords Medicine ; R ; Science ; Q
    Subject code 500
    Language English
    Publishing date 2022-10-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Urinary miRNA-27b-3p and miRNA-1228-3p correlate with the progression of Kidney Fibrosis in Diabetic Nephropathy.

    Conserva, Francesca / Barozzino, Mariagrazia / Pesce, Francesco / Divella, Chiara / Oranger, Annarita / Papale, Massimo / Sallustio, Fabio / Simone, Simona / Laviola, Luigi / Giorgino, Francesco / Gallone, Anna / Pontrelli, Paola / Gesualdo, Loreto

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 11357

    Abstract: Diabetic Nephropathy (DN) is a chronic complication of diabetes and the primary cause of end stage renal disease. Differential diagnosis for DN requires invasive histological investigation, thus there is need for non-invasive biomarkers to discriminate ... ...

    Abstract Diabetic Nephropathy (DN) is a chronic complication of diabetes and the primary cause of end stage renal disease. Differential diagnosis for DN requires invasive histological investigation, thus there is need for non-invasive biomarkers to discriminate among different histological lesions in diabetic patients. With the aim to identify a pattern of differentially expressed miRNAs in kidney biopsies of DN patients, we assayed miRNA expression in kidney biopsies from DN patients, diabetic patients with membranous nephropathy and patients with normal histology. Nine miRNAs were differentially expressed among the three groups, and 2 miRNAs (miR-27b-3p and miR-1228-3p) showed interaction with an ubiquitin-conjugating E2 enzyme variant (UBE2v1). UBE2v1 mediates the formation of lysine 63-linked ubiquitin chains, a mechanism we previously showed as involved in DN kidney fibrosis. Both miRNAs were validated as down-regulated in biopsies and urines of DN patients, possibly affected by DNA methylation. Interestingly, the urinary levels of both miRNAs could also discriminate among different degrees of renal fibrosis. Finally, we showed that the combined urinary expression of both miRNAs was also able to discriminate DN patients from other glomerulonephritides in diabetic patients. In conclusion we identified two miRNAs potentially useful as candidate biomarkers of tubular-interstitial fibrosis in diabetic patients with DN.
    MeSH term(s) Adult ; Aged ; Biomarkers/urine ; Diabetic Nephropathies/complications ; Disease Progression ; Female ; Fibrosis/etiology ; Fibrosis/genetics ; Fibrosis/metabolism ; Fibrosis/urine ; Gene Expression Regulation ; Humans ; Kidney/metabolism ; Kidney Diseases/etiology ; Kidney Diseases/genetics ; Kidney Diseases/metabolism ; Kidney Diseases/urine ; Male ; MicroRNAs/genetics ; MicroRNAs/urine ; Middle Aged
    Chemical Substances Biomarkers ; MIRN1228 microRNA, human ; MIRN27b microRNA, human ; MicroRNAs
    Language English
    Publishing date 2019-08-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-47778-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Urinary miRNA-27b-3p and miRNA-1228-3p correlate with the progression of Kidney Fibrosis in Diabetic Nephropathy

    Francesca Conserva / Mariagrazia Barozzino / Francesco Pesce / Chiara Divella / Annarita Oranger / Massimo Papale / Fabio Sallustio / Simona Simone / Luigi Laviola / Francesco Giorgino / Anna Gallone / Paola Pontrelli / Loreto Gesualdo

    Scientific Reports, Vol 9, Iss 1, Pp 1-

    2019  Volume 11

    Abstract: Abstract Diabetic Nephropathy (DN) is a chronic complication of diabetes and the primary cause of end stage renal disease. Differential diagnosis for DN requires invasive histological investigation, thus there is need for non-invasive biomarkers to ... ...

    Abstract Abstract Diabetic Nephropathy (DN) is a chronic complication of diabetes and the primary cause of end stage renal disease. Differential diagnosis for DN requires invasive histological investigation, thus there is need for non-invasive biomarkers to discriminate among different histological lesions in diabetic patients. With the aim to identify a pattern of differentially expressed miRNAs in kidney biopsies of DN patients, we assayed miRNA expression in kidney biopsies from DN patients, diabetic patients with membranous nephropathy and patients with normal histology. Nine miRNAs were differentially expressed among the three groups, and 2 miRNAs (miR-27b-3p and miR-1228-3p) showed interaction with an ubiquitin-conjugating E2 enzyme variant (UBE2v1). UBE2v1 mediates the formation of lysine 63-linked ubiquitin chains, a mechanism we previously showed as involved in DN kidney fibrosis. Both miRNAs were validated as down-regulated in biopsies and urines of DN patients, possibly affected by DNA methylation. Interestingly, the urinary levels of both miRNAs could also discriminate among different degrees of renal fibrosis. Finally, we showed that the combined urinary expression of both miRNAs was also able to discriminate DN patients from other glomerulonephritides in diabetic patients. In conclusion we identified two miRNAs potentially useful as candidate biomarkers of tubular-interstitial fibrosis in diabetic patients with DN.
    Keywords Medicine ; R ; Science ; Q
    Subject code 610 ; 616
    Language English
    Publishing date 2019-08-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Deregulation of autophagy under hyperglycemic conditions is dependent on increased lysine 63 ubiquitination: a candidate mechanism in the progression of diabetic nephropathy.

    Pontrelli, Paola / Oranger, Annarita / Barozzino, Mariagrazia / Divella, Chiara / Conserva, Francesca / Fiore, Maria Grazia / Rossi, Roberta / Papale, Massimo / Castellano, Giuseppe / Simone, Simona / Laviola, Luigi / Giorgino, Francesco / Piscitelli, Domenico / Gallone, Anna / Gesualdo, Loreto

    Journal of molecular medicine (Berlin, Germany)

    2018  Volume 96, Issue 7, Page(s) 645–659

    Abstract: Diabetic nephropathy patients (DN) are characterized by increased lysine63 ubiquitination (Lys63-Ub) at the tubular level. Autophagy is deregulated under diabetic conditions, even though the molecular mechanisms and the consequences of this alteration ... ...

    Abstract Diabetic nephropathy patients (DN) are characterized by increased lysine63 ubiquitination (Lys63-Ub) at the tubular level. Autophagy is deregulated under diabetic conditions, even though the molecular mechanisms and the consequences of this alteration need to be elucidated. The aim of this study was to investigate the link between Lys63-Ub and autophagy in DN and the involvement of these two processes in tubular cell fate. Immunohistochemistry of beclin-1, LC3, and p62 on kidney biopsies highlighted increased protein expression of all these autophagic factors at the tubular level in DN compared to other nephritis. Transmission electron microscopy confirmed the presence of diffuse vacuolization and autophago(lyso)somal structures in proximal tubular cells in DN. Accumulation of Lys63-Ub proteins in DN increased in accordance with the tubular damage and was associated to increased LC3 expression both in vivo and in vitro. Hyperglycemia (HG) induced LC3 and p62 protein expression in HK2 cells together with Lys63-ubiquitinated proteins, and the inhibition of HG-induced Lys63-Ub by NSC697923 inhibitor, significantly reduced both LC3 and p62 expression. Moreover, in DN, those tubules expressing LC3 showed increased caspase-3 expression, supporting the hypothesis that deregulated autophagy induces apoptosis of tubular cells. In vitro, we confirmed a tight association between impaired autophagy, Lys63-Ub, and apoptosis since Lys63-Ub inhibition by NSC697923 abrogated HG-induced cell death and LC3 silencing also blocked hyperglycemia-induced caspase-3 activation. Our data suggested that prolonged hyperglycemia in diabetic patients can impair autophagy as a consequence of Lys63-Ub protein accumulation, thus promoting intracellular autophagic vesicles increase, finally leading to tubular cell death in DN.
    Key messages: In vivo autophagy is deregulated in diabetic patients with renal disease (DN). Accumulation of Lys63 ubiquitinated proteins is associated to autophagy deregulation. Accumulation of Lys63 ubiquitinated proteins correlated with apoptosis activation. Lys63 ubiquitination inhibition abrogated hyperglycemia-induced autophagy and apoptosis.
    MeSH term(s) Adult ; Apoptosis ; Apoptosis Regulatory Proteins/genetics ; Apoptosis Regulatory Proteins/metabolism ; Autophagy ; Diabetic Nephropathies/etiology ; Diabetic Nephropathies/metabolism ; Diabetic Nephropathies/pathology ; Disease Progression ; Epithelial Cells/metabolism ; Epithelial Cells/pathology ; Female ; Fluorescent Antibody Technique ; Gene Expression ; Gene Silencing ; Humans ; Hyperglycemia/genetics ; Hyperglycemia/metabolism ; Immunohistochemistry ; Kidney Tubules/metabolism ; Kidney Tubules/pathology ; Kidney Tubules/ultrastructure ; Lysine/metabolism ; Male ; Microtubule-Associated Proteins/genetics ; Microtubule-Associated Proteins/metabolism ; Middle Aged ; Ubiquitination
    Chemical Substances Apoptosis Regulatory Proteins ; MAP1LC3A protein, human ; Microtubule-Associated Proteins ; Lysine (K3Z4F929H6)
    Language English
    Publishing date 2018-05-27
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1223802-8
    ISSN 1432-1440 ; 0946-2716
    ISSN (online) 1432-1440
    ISSN 0946-2716
    DOI 10.1007/s00109-018-1656-3
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  10. Article ; Online: Lysine 63 ubiquitination is involved in the progression of tubular damage in diabetic nephropathy.

    Pontrelli, Paola / Conserva, Francesca / Papale, Massimo / Oranger, Annarita / Barozzino, Mariagrazia / Vocino, Grazia / Rocchetti, Maria Teresa / Gigante, Margherita / Castellano, Giuseppe / Rossini, Michele / Simone, Simona / Laviola, Luigi / Giorgino, Francesco / Grandaliano, Giuseppe / Di Paolo, Salvatore / Gesualdo, Loreto

    FASEB journal : official publication of the Federation of American Societies for Experimental Biology

    2017  Volume 31, Issue 1, Page(s) 308–319

    Abstract: ... interstitial fibrosis in patients with DN.-Pontrelli, P., Conserva, F., Papale, M., Oranger, A., Barozzino, M ...

    Abstract The purpose of our study was to evaluate how hyperglycemia (HG) influences Lys63 protein ubiquitination and its involvement in tubular damage and fibrosis in diabetic nephropathy (DN). Gene and protein expression of UBE2v1, a ubiquitin-conjugating E2-enzyme variant that mediates Lys63-linked ubiquitination, and Lys63-ubiquitinated proteins increased in HK2 tubular cells under HG. Matrix-assisted laser desorption/ionization-time of flight/tandem mass spectrometry identified 30 Lys63-ubiquitinated proteins, mainly involved in cellular organization, such as β-actin, whose Lys63 ubiquitination increased under HG, leading to cytoskeleton disorganization. This effect was reversed by the inhibitor of the Ubc13/UBE2v1 complex NSC697923. Western blot analysis confirmed that UBE2v1 silencing in HK2 under HG, restored Lys63-β-actin ubiquitination levels to the basal condition. Immunohistochemistry on patients with type 2 diabetic (T2D) revealed an increase in UBE2v1- and Lys63-ubiquitinated proteins, particularly in kidneys of patients with DN compared with control kidneys and other nondiabetic renal diseases, such as membranous nephropathy. Increased Lys63 ubiquitination both in vivo in patients with DN and in vitro, correlated with α-SMA expression, whereas UBE2v1 silencing reduced HG-induced α-SMA protein levels, returning them to basal expression. In conclusion, UBE2v1- and Lys63-ubiquitinated proteins increase in vitro under HG, as well as in vivo in T2D, is augmented in patients with DN, and may affect cytoskeleton organization and influence epithelial-to-mesenchymal transition. This process may drive the progression of tubular damage and interstitial fibrosis in patients with DN.-Pontrelli, P., Conserva, F., Papale, M., Oranger, A., Barozzino, M., Vocino, G., Rochetti, M. T., Gigante, M., Castellano, G., Rossini, M., Simone, S., Laviola, L., Giorgino, F., Grandaliano, G., Di Paolo, S., Gesualdo, L. Lysine 63 ubiquitination is involved in the progression of tubular damage in diabetic nephropathy.
    MeSH term(s) Amino Acid Sequence ; Biomarkers ; Cell Line ; Diabetic Nephropathies/metabolism ; Epithelial Cells/metabolism ; Gene Expression Regulation/physiology ; Gene Silencing ; Humans ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Ubiquitin-Conjugating Enzymes/genetics ; Ubiquitin-Conjugating Enzymes/metabolism ; Ubiquitinated Proteins ; Ubiquitination/physiology
    Chemical Substances Biomarkers ; Transcription Factors ; Ubiquitinated Proteins ; UBE2V1 protein, human (EC 2.3.2.23) ; Ubiquitin-Conjugating Enzymes (EC 2.3.2.23)
    Language English
    Publishing date 2017-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 639186-2
    ISSN 1530-6860 ; 0892-6638
    ISSN (online) 1530-6860
    ISSN 0892-6638
    DOI 10.1096/fj.201600382RR
    Database MEDical Literature Analysis and Retrieval System OnLINE

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