Gabriele colangelo biography of albert einstein

Editorial board

Editor-in-Chief                                             
Uberto Pagotto, MD, PhD, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy

Editor-in-Chief Emeritus
Luigi Bartalena, MD, PhD, University of Insubria, Varese, Italy

Associate Editors
Barbara Altieri, MD, University of Würzburg, Würzburg, Germany
Moufida Ben Nasr, PhD, Boston Children's Hospital, Boston, MA, United States of America
Sanjay Bhadada, MD, PhD, PGIMER, Chaudigah , India
Carla Bizzarri, MD, PhD, Bambino Gesù Children's Hospital, Rome, Italy
Karim Bouzakri, MD, Université de Strasbourg, Strasbourg , France
Philippe Caron, PhD, CHU de Toulouse - Hôpital Larrey, Toulouse, France
Maria Grazia Castagna, MD, PhD, University of Siena, Siena, Italy
Giovanni Ceccarini, MD, Obesity and Lipodystrophy Center, University Hospital of Pisa, Pisa, Italy
Filomena Cetani, MD, University of Pisa, Pisa, Italy
Luisella Cianferotti, MD, PhD, Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy
Giovanni Corona, MD, PhD, Maggiore Hospital Bologna, Bologna, Italy
Daniela Cota, MD, INSERM, University of Bordeaux, Bordeaux, France
Francis De Zegher, PhD, KU Leuven, Leuven, Belgium
Maria Cristina De Martino, MD, PhD, University of Naples Federico II, Naples, Italy
Guido di Dalmazi, MD, PhD, University of Bologna, Bologna, Italy
Rossella Elisei, MD, PhD, University of Pisa, Pisa, Italy
Daniela Esposito, MD, University of Gothenburg, Gothenburg, Sweden
Antongiulio Faggiano, PhD, University Sapienza, Rome, Italy
Paolo Fiorina, MD, PhD, Boston University, Boston, MA, United States of America
Lucia Frittitta, MD, PhD, University of Catania, Catania, I

  • Colangelo Gilberto, Prof. Dr. Position:
  • Gilberto Colangelo did his
  • Gaia contributors

     

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  • Albert Cossery; Albert Einstein; Alberte Lauridsen;
  • . Author manuscript; available in PMC: 2009 Mar 26.

    Published in final edited form as: Neuroscience. 2007 Apr 11;146(3):1150–1157. doi: 10.1016/j.neuroscience.2007.02.042

    Abstract

    Prostaglandins (PGs) are bioactive lipid mediators released following brain hypoxic-ischemic injury. Clearance and re-uptake of these prostaglandins occur via a transmembrane prostaglandin transporter (PGT), which exchanges PG for lactate. We used western blot analyses to examine the PGT developmental profile and its regional distribution as well as changes in transporter expression during chronic hypoxia. Microsomal preparations from four brain regions (cortex, hippocampus, cerebellum and brainstem/diencephalon) showed gradual increases in prostaglandin transporter expression in all brain regions examined from postnatal day 1 till day 30. There was a significant regional heterogeneity in the prostaglandin transporter expression with highest expression in the cortex, followed by cerebellum and hippocampus, and least expressed in the brainstem-diencephalon. To further delineate the pattern of prostaglandin transporter expression, separate astrocytic and neuronal microsomal preparations were also examined. In contrast to neurons, which had a robust expression of prostaglandin transporters, astrocytes had very little PGT expression under basal conditions. In response to chronic hypoxia, there was a significant decline in PGT expression in vivo and in neurons in vitro, whereas cultured astrocytes increased their PGT expression. This is the first report on PGT expression in the central nervous system (CNS) and our studies suggest that PGTs have 1) a widespread distribution in the CNS; 2) a gradual increase and a differential expression in various regions during brain development; and 3) striking contrast in expression between glia and neurons, especially in response to hypoxia. Since PGTs play a role as prostaglandin-lactate exchangers, we hypothesize that PGTs are important in the CNS

    Open Access

    Peer-reviewed

    • Francesca Oltolina ,
    • Andrea Zamperone ,
    • Donato Colangelo,
    • Luca Gregoletto,
    • Simone Reano,
    • Stefano Pietronave,
    • Simone Merlin,
    • Maria Talmon,
    • Eugenio Novelli,
    • Marco Diena,
    • Carmine Nicoletti,
    • Antonio Musarò,
    • Nicoletta Filigheddu,
    • Antonia Follenzi,
    • Maria Prat
    • Francesca Oltolina, 
    • Andrea Zamperone, 
    • Donato Colangelo, 
    • Luca Gregoletto, 
    • Simone Reano, 
    • Stefano Pietronave, 
    • Simone Merlin, 
    • Maria Talmon, 
    • Eugenio Novelli, 
    • Marco Diena

    x

    Correction

    Abstract

    A major obstacle to an effective myocardium stem cell therapy has always been the delivery and survival of implanted stem cells in the heart. Better engraftment can be achieved if cells are administered as cell aggregates, which maintain their extra-cellular matrix (ECM). We have generated spheroid aggregates in less than 24 h by seeding human cardiac progenitor cells (hCPCs) onto methylcellulose hydrogel-coated microwells. Cells within spheroids maintained the expression of stemness/mesenchymal and ECM markers, growth factors and their cognate receptors, cardiac commitment factors, and metalloproteases, as detected by immunofluorescence, q-RT-PCR and immunoarray, and expressed a higher, but regulated, telomerase activity. Compared to cells in monolayers, 3D spheroids secreted also bFGF and showed MMP2 activity. When spheroids were seeded on culture plates, the cells quickly migrated, displaying an increased wound healing ability with or without pharmacological modulation, and reached confluence at a higher rate than cells from conventional monolayers. When spheroids were injected in the heart wall of healthy mice, some cells migrated from the spheroids, engrafted, and remained detectable for at least 1 week after transplantation, while, when the same amount of cells was injected as suspension, no cells were detectable three days after injection. Cells from spheroids displaye

  • Gabrielle Colangelo '22 brings obscured lesbian