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  1. AU="Scott M. Riester"
  2. AU="A Zappa, Marco"
  3. AU=Panciani Pier Paolo
  4. AU="La Cascio, L"
  5. AU="Getsuwan, Songpon"

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  1. Artikel: Molecular landscape of arthrofibrosis: Microarray and bioinformatic analysis of the temporal expression of 380 genes during contracture genesis

    Morrey, Mark E / Amel Dudakovic / Andre J. van Wijnen / Bernard F. Morrey / Joaquin Sanchez-Sotelo / Matthew P. Abdel / Scott M. Riester

    Gene. 2017 Apr. 30, v. 610

    2017  

    Abstract: Inflammatory changes are suspected in the pathophysiology of arthrofibrosis formation and require early molecular examination. Here, we assessed the hypothesis that early inflammatory genes are related to arthrofibrosis by ascertaining gene expression ... ...

    Abstract Inflammatory changes are suspected in the pathophysiology of arthrofibrosis formation and require early molecular examination. Here, we assessed the hypothesis that early inflammatory genes are related to arthrofibrosis by ascertaining gene expression during the early stages of contracture genesis in an animal model.Joint trauma was incited surgically in a cohort of rabbits (n=36) knees followed by immobilization in a model of contracture. Six groups of 6 rabbits were sacrificed at multiple time points (0, 6, 12, 24, 72h and 2weeks). Microarray expression and RT-qPCR profiling were performed to determine genes that are significantly up or downregulated. Bioinformatic analysis was carried out to understand which biological programs and functional groups of genes are modulated in arthrofibrosis.Gene expression profiling revealed a large number biologically relevant genes (>100) that are either upregulated or downregulated by at least a 1.5 fold (log2) during the first two weeks after joint injury during contracture development. Gene ontology analysis identified molecular pathways and programs that act during the course of fibrosis and joint contracture. Our main finding is that the development of contractures occur concomitant with modulation of genes mediating inflammatory responses, ECM remodeling and the epithelial-to-mesenchymal transition.The genesis of joint contracture reflects an imbalance between pro- and anti-fibrotic expression. Our study indicates that inflammatory genes may be involved in the process of contracture genesis and initiated at relatively early stages. Our findings also may inform clinical practice in the future by suggesting potential therapeutic targets in preventing the long-term development of arthrofibrosis.
    Schlagwörter bioinformatics ; contracture ; fibrosis ; gene expression ; gene expression regulation ; gene ontology ; genes ; inflammation ; knees ; microarray technology ; models ; pathophysiology ; quantitative polymerase chain reaction ; rabbits ; reverse transcriptase polymerase chain reaction
    Sprache Englisch
    Erscheinungsverlauf 2017-0430
    Umfang p. 15-23.
    Erscheinungsort Elsevier B.V.
    Dokumenttyp Artikel
    ZDB-ID 391792-7
    ISSN 1879-0038 ; 0378-1119
    ISSN (online) 1879-0038
    ISSN 0378-1119
    DOI 10.1016/j.gene.2017.01.025
    Datenquelle NAL Katalog (AGRICOLA)

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  2. Artikel: Inhibiting DNA-PKCS radiosensitizes human osteosarcoma cells

    Mamo, Tewodros / Andre J. van Wijnen / Ann C. Mladek / Avudaiappan Maran / Carl Gustafson / Jann N. Sarkaria / Kris L. Shogren / Mario Galindo / Michael J. Yaszemski / Scott M. Riester / Shiv K. Gupta

    Biochemical and biophysical research communications. 2017 Apr. 29, v. 486

    2017  

    Abstract: Osteosarcoma survival rate has not improved over the past three decades, and the debilitating side effects of the surgical treatment suggest the need for alternative local control approaches. Radiotherapy is largely ineffective in osteosarcoma, ... ...

    Abstract Osteosarcoma survival rate has not improved over the past three decades, and the debilitating side effects of the surgical treatment suggest the need for alternative local control approaches. Radiotherapy is largely ineffective in osteosarcoma, indicating a potential role for radiosensitizers. Blocking DNA repair, particularly by inhibiting the catalytic subunit of DNA-dependent protein kinase (DNA-PKCS), is an attractive option for the radiosensitization of osteosarcoma. In this study, the expression of DNA-PKCS in osteosarcoma tissue specimens and cell lines was examined. Moreover, the small molecule DNA-PKCS inhibitor, KU60648, was investigated as a radiosensitizing strategy for osteosarcoma cells in vitro. DNA-PKCS was consistently expressed in the osteosarcoma tissue specimens and cell lines studied. Additionally, KU60648 effectively sensitized two of those osteosarcoma cell lines (143B cells by 1.5-fold and U2OS cells by 2.5-fold). KU60648 co-treatment also altered cell cycle distribution and enhanced DNA damage. Cell accumulation at the G2/M transition point increased by 55% and 45%, while the percentage of cells with >20 γH2AX foci were enhanced by 59% and 107% for 143B and U2OS cells, respectively. These results indicate that the DNA-PKCS inhibitor, KU60648, is a promising radiosensitizing agent for osteosarcoma.
    Schlagwörter cell cycle ; DNA damage ; DNA repair ; humans ; osteosarcoma ; protein subunits ; survival rate
    Sprache Englisch
    Erscheinungsverlauf 2017-0429
    Umfang p. 307-313.
    Erscheinungsort Elsevier Inc.
    Dokumenttyp Artikel
    ZDB-ID 205723-2
    ISSN 0006-291X ; 0006-291X
    ISSN (online) 0006-291X
    ISSN 0006-291X
    DOI 10.1016/j.bbrc.2017.03.033
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel ; Online: Intrarenal Delivery of Mesenchymal Stem Cells and Endothelial Progenitor Cells Attenuates Hypertensive Cardiomyopathy in Experimental Renovascular Hypertension

    Alfonso Eirin / Xiang-Yang Zhu / Behzad Ebrahimi / James D. Krier / Scott M. Riester / Andre J. Van Wijnen / Amir Lerman / Lilach O. Lerman M.D., Ph.D.

    Cell Transplantation, Vol

    2015  Band 24

    Abstract: Renovascular hypertension (RVH) leads to left ventricular (LV) hypertrophy and diastolic dysfunction, associated with increased cardiovascular mortality. Intrarenal delivery of endothelial progenitor cells (EPCs) and mesenchymal stem cells (MSCs) ... ...

    Abstract Renovascular hypertension (RVH) leads to left ventricular (LV) hypertrophy and diastolic dysfunction, associated with increased cardiovascular mortality. Intrarenal delivery of endothelial progenitor cells (EPCs) and mesenchymal stem cells (MSCs) improves kidney function in porcine RVH, and the potent anti-inflammatory properties of MSCs may serve to blunt inflammatory mediators in the cardiorenal axis. However, their relative efficacy in attenuating cardiac injury and dysfunction remains unknown. This study tested the hypothesis that the car-dioprotective effect of EPCs and MSCs delivered into the stenotic kidney in experimental RVH are comparable. Pigs ( n = 7 per group) were studied after 10 weeks of RVH or control untreated or treated with a single intrarenal infusion of autologous EPCs or MSCs 4 weeks earlier. Cardiac and renal function (fast CT) and stenotic kidney release of inflammatory mediators (ELISA) were assessed in vivo, and myocardial inflammation, remodeling, and fibrosis ex vivo. After 10 weeks of RVH, blood pressure was not altered in cell-treated groups, yet stenotic kidney glomerular filtration rate (GFR), blunted in RVH, improved in RVH + EPC, and normalized in RVH + MSCs. Stenotic kidney release of monocyte chemoattractant protein (MCP)-1 and its myocardial expression were elevated in RVH + EPC, but normalized only in RVH + MSC pigs. RVH-induced LV hypertrophy was normalized in both EPC- and MSC-treated pigs, while diastolic function (E/A ratio) was restored to normal levels exclusively in RVH + MSCs. RVH-induced myocardial fibrosis and collagen deposition decreased in RVH + EPCs but further decreased in RVH + MSC-treated pigs. Intrarenal delivery of EPCs or MSCs attenuates RVH-induced myocardial injury, yet MSCs restore diastolic function more effectively than EPCs, possibly by greater improvement in renal function or reduction of MCP-1 release from the stenotic kidney. These observations suggest a therapeutic potential for EPCs and MSCs in preserving the myocardium in chronic experimental ...
    Schlagwörter Medicine ; R
    Thema/Rubrik (Code) 616
    Sprache Englisch
    Erscheinungsdatum 2015-10-01T00:00:00Z
    Verlag SAGE Publishing
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  4. Artikel: MicroRNA and mRNA cargo of extracellular vesicles from porcine adipose tissue-derived mesenchymal stem cells

    Eirin, Alfonso / Andre J. van Wijnen / Daniel O'Brien / Hui Tang / Jared M. Evans / Lilach O. Lerman / Scott M. Riester / Xiang-Yang Zhu

    Gene. 2014 Nov. 01, v. 551

    2014  

    Abstract: Mesenchymal stromal/stem cells (MSCs) are clinically useful for cell-based therapy, but concerns regarding their ability to replicate limit their human application. MSCs release extracellular vesicles (EVs) that mediate at least in part the paracrine ... ...

    Abstract Mesenchymal stromal/stem cells (MSCs) are clinically useful for cell-based therapy, but concerns regarding their ability to replicate limit their human application. MSCs release extracellular vesicles (EVs) that mediate at least in part the paracrine effects of the parental cells. To understand the molecular basis of their biological properties, we characterized the RNA cargo of EVs from porcine adipose-tissue derived MSCs. Comprehensive characterization of mRNA and miRNA gene expression using high-throughput RNA sequencing (RNA-seq) revealed that EVs are selectively enriched for distinct classes of RNAs. For example, EVs preferentially express mRNA for transcription factors (e.g. MDFIC, POU3F1, NRIP1) and genes involved in angiogenesis (e.g. HGF, HES1, TCF4) and adipogenesis (e.g. CEBPA, KLF7). EVs also express Golgi apparatus genes (ARRB1, GOLGA4) and genes involved in TGF-β signaling. In contrast, mitochondrial, calcium signaling, and cytoskeleton genes are selectively excluded from EVs, possibly because these genes remain sequestered in organelles or intracellular compartments. RNA-seq generated reads for at least 386 annotated miRNAs, but only miR148a, miR532-5p, miR378, and let-7f were enriched in EVs compared to MSCs. Gene ontology analysis indicates that these miRNAs target transcription factors and genes that participate in several cellular pathways, including angiogenesis, cellular transport, apoptosis, and proteolysis. Our data suggest that EVs transport gene regulatory information to modulate angiogenesis, adipogenesis, and other cell pathways in recipient cells. These observations may contribute to development of regenerative strategies using EVs to overcome potential complications of cell-based therapy.
    Schlagwörter adipogenesis ; adipose tissue ; angiogenesis ; apoptosis ; calcium signaling ; cytoskeleton ; gene expression ; Golgi apparatus ; high-throughput nucleotide sequencing ; humans ; messenger RNA ; microRNA ; mitochondria ; proteolysis ; stem cells ; swine ; therapeutics ; transcription factors ; transforming growth factor beta
    Sprache Englisch
    Erscheinungsverlauf 2014-1101
    Umfang p. 55-64.
    Erscheinungsort Elsevier B.V.
    Dokumenttyp Artikel
    ZDB-ID 391792-7
    ISSN 1879-0038 ; 0378-1119
    ISSN (online) 1879-0038
    ISSN 0378-1119
    DOI 10.1016/j.gene.2014.08.041
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  5. Artikel ; Online: Mapping molecular landmarks of human skeletal ontogeny and pluripotent stem cell-derived articular chondrocytes

    Gabriel B. Ferguson / Ben Van Handel / Maxwell Bay / Petko Fiziev / Tonis Org / Siyoung Lee / Ruzanna Shkhyan / Nicholas W. Banks / Mila Scheinberg / Ling Wu / Biagio Saitta / Joseph Elphingstone / A. Noelle Larson / Scott M. Riester / April D. Pyle / Nicholas M. Bernthal / Hanna KA Mikkola / Jason Ernst / Andre J. van Wijnen /
    Michael Bonaguidi / Denis Evseenko

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Band 16

    Abstract: Human development provides a roadmap for advancing pluripotent stem cell-based regenerative therapies. Here the authors mapped human skeletogenesis using RNA sequencing on 5 cell types from a single foetal stage as well as chondrocytes at 4 stages in ... ...

    Abstract Human development provides a roadmap for advancing pluripotent stem cell-based regenerative therapies. Here the authors mapped human skeletogenesis using RNA sequencing on 5 cell types from a single foetal stage as well as chondrocytes at 4 stages in vivo and 2 stages during in vitro differentiation.
    Schlagwörter Science ; Q
    Sprache Englisch
    Erscheinungsdatum 2018-09-01T00:00:00Z
    Verlag Nature Portfolio
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  6. Artikel ; Online: Mapping molecular landmarks of human skeletal ontogeny and pluripotent stem cell-derived articular chondrocytes

    Gabriel B. Ferguson / Ben Van Handel / Maxwell Bay / Petko Fiziev / Tonis Org / Siyoung Lee / Ruzanna Shkhyan / Nicholas W. Banks / Mila Scheinberg / Ling Wu / Biagio Saitta / Joseph Elphingstone / A. Noelle Larson / Scott M. Riester / April D. Pyle / Nicholas M. Bernthal / Hanna KA Mikkola / Jason Ernst / Andre J. van Wijnen /
    Michael Bonaguidi / Denis Evseenko

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Band 16

    Abstract: Human development provides a roadmap for advancing pluripotent stem cell-based regenerative therapies. Here the authors mapped human skeletogenesis using RNA sequencing on 5 cell types from a single foetal stage as well as chondrocytes at 4 stages in ... ...

    Abstract Human development provides a roadmap for advancing pluripotent stem cell-based regenerative therapies. Here the authors mapped human skeletogenesis using RNA sequencing on 5 cell types from a single foetal stage as well as chondrocytes at 4 stages in vivo and 2 stages during in vitro differentiation.
    Schlagwörter Science ; Q
    Sprache Englisch
    Erscheinungsdatum 2018-09-01T00:00:00Z
    Verlag Nature Publishing Group
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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