LIVIVO - Das Suchportal für Lebenswissenschaften

switch to English language
Erweiterte Suche

Ihre letzten Suchen

  1. AU="Fabio Sallustio"
  2. AU=Fahde Youssef
  3. AU=Jones M Lloyd
  4. AU="Sorn, San"
  5. AU="Gamoudi Amel"
  6. AU=Weidner Lisa AU=Weidner Lisa
  7. AU="Park, Donghee"
  8. AU="Daniel Paull"
  9. AU="H Divecha"
  10. AU="Chetata, Nabil"
  11. AU="Zuo, Nan"
  12. AU="Lin, Raymond Tzer-Pin"
  13. AU="Whittington, Karen B"
  14. AU="Beutel, Gernot"
  15. AU="Koh, Siang Boon"
  16. AU="Rajki, Anikó"
  17. AU="Polina B. Drozdova"
  18. AU=Zhang Xiuhong AU=Zhang Xiuhong
  19. AU=Hauer Julia
  20. AU="Widiasih, Natalia"
  21. AU="Besnik Bajrami"
  22. AU=Mazza Mario Gennaro
  23. AU="Kwong, A S K"
  24. AU="Hadian, Marziye"
  25. AU="Chen, Yaying"
  26. AU="Ortega, Francisco B"
  27. AU=Cobb Samuel N
  28. AU="Abdelmohssin El Mokaddem"
  29. AU="Iwao Ojima"
  30. AU="Abazi, Sokol"
  31. AU="Cook, Rebecca"
  32. AU=Martin Flavius
  33. AU="Cipriani, Raffaela"
  34. AU="Levin, Michael E."
  35. AU="Yang, Dayu"

Suchergebnis

Treffer 1 - 10 von insgesamt 22

Suchoptionen

  1. Artikel ; Online: Editorial

    Roberto Gramignoli / Fabio Sallustio / Darius Widera

    Frontiers in Medicine, Vol

    Repair and regenerative mechanisms by stem/progenitor cells and secretome: The golden twenties of translational medicine

    2022  Band 9

    Schlagwörter cell-based medicinal products ; secretome ; translational applications ; regenerative medicine ; secreted metabolites ; Medicine (General) ; R5-920
    Sprache Englisch
    Erscheinungsdatum 2022-08-01T00:00:00Z
    Verlag Frontiers Media S.A.
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  2. Artikel ; Online: Pulsed Electromagnetic Fields Induce Skeletal Muscle Cell Repair by Sustaining the Expression of Proteins Involved in the Response to Cellular Damage and Oxidative Stress

    Silvia Maiullari / Antonella Cicirelli / Angela Picerno / Francesca Giannuzzi / Loreto Gesualdo / Angela Notarnicola / Fabio Sallustio / Biagio Moretti

    International Journal of Molecular Sciences, Vol 24, Iss 23, p

    2023  Band 16631

    Abstract: Pulsed electromagnetic fields (PEMF) are employed as a non-invasive medicinal therapy, especially in the orthopedic field to stimulate bone regeneration. However, the effect of PEMF on skeletal muscle cells (SkMC) has been understudied. Here, we studied ... ...

    Abstract Pulsed electromagnetic fields (PEMF) are employed as a non-invasive medicinal therapy, especially in the orthopedic field to stimulate bone regeneration. However, the effect of PEMF on skeletal muscle cells (SkMC) has been understudied. Here, we studied the potentiality of 1.5 mT PEMF to stimulate early regeneration of human SkMC. We showed that human SkMC stimulated with 1.5 mT PEMF for four hours repeated for two days can stimulate cell proliferation without inducing cell apoptosis or significant impairment of the metabolic activity. Interestingly, when we simulated physical damage of the muscle tissue by a scratch, we found that the same PEMF treatment can speed up the regenerative process, inducing a more complete cell migration to close the scratch and wound healing. Moreover, we investigated the molecular pattern induced by PEMF among 26 stress-related cell proteins. We found that the expression of 10 proteins increased after two consecutive days of PEMF stimulation for 4 h, and most of them were involved in response processes to oxidative stress. Among these proteins, we found that heat shock protein 70 (HSP70), which can promote muscle recovery, inhibits apoptosis and decreases inflammation in skeletal muscle, together with thioredoxin, paraoxonase, and superoxide dismutase (SOD2), which can also promote skeletal muscle regeneration following injury. Altogether, these data support the possibility of using PEMF to increase SkMC regeneration and, for the first time, suggest a possible molecular mechanism, which consists of sustaining the expression of antioxidant enzymes to control the important inflammatory and oxidative process occurring following muscle damage.
    Schlagwörter PEMF ; skeletal muscle cells ; cellular damage ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2023-11-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  3. Artikel ; Online: Editorial

    Roberto Gramignoli / Fabio Sallustio / Darius Widera / Nathanael Raschzok

    Frontiers in Medicine, Vol

    Tissue Repair and Regenerative Mechanisms by Stem/Progenitor Cells and Their Secretome

    2019  Band 6

    Schlagwörter tissue repair and regeneration ; regenerative mechanism ; stem cells ; progenitor cells ; secretome ; Medicine (General) ; R5-920
    Sprache Englisch
    Erscheinungsdatum 2019-01-01T00:00:00Z
    Verlag Frontiers Media S.A.
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  4. Artikel ; Online: Clinical Application of Human Urinary Extracellular Vesicles in Kidney and Urologic Diseases

    Giuseppe De Palma / Fabio Sallustio / Francesco Paolo Schena

    International Journal of Molecular Sciences, Vol 17, Iss 7, p

    2016  Band 1043

    Abstract: Extracellular vesicles (EVs) have been isolated in different body fluids, including urine. The cargo of urinary EVs is composed of nucleic acids and proteins reflecting the physiological and possibly pathophysiological state of cells lining the nephron ... ...

    Abstract Extracellular vesicles (EVs) have been isolated in different body fluids, including urine. The cargo of urinary EVs is composed of nucleic acids and proteins reflecting the physiological and possibly pathophysiological state of cells lining the nephron and the urinary tract. Urinary EVs have been confirmed to contain low amounts of various types of RNA that play a role in intercellular communication by transferring genetic information. This communication through EV RNAs includes both continuation of normal physiological processes and conditioning in disease mechanisms. Although proteins included in urinary EVs represent only 3% of the whole-urine proteome, urinary EVs can influence cells in the renal epithelia not only by delivering RNA cargo, but also by delivering a wide range of proteins. Since urine is a readily available biofluid, the discovery of EVs has opened a new field of biomarker research. The potential use of urinary EV RNAs and proteins as diagnostic biomarkers for various kidney and urologic diseases is currently being explored. Here, we review recent studies that deal in identifying biomarker candidates for human kidney and urologic diseases using urinary EVs and might help to understand the pathophysiology.
    Schlagwörter extracellular vesicles ; urine ; kidney diseases ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Sprache Englisch
    Erscheinungsdatum 2016-06-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  5. Artikel ; Online: A New Vision of IgA Nephropathy

    Fabio Sallustio / Claudia Curci / Vincenzo Di Leo / Anna Gallone / Francesco Pesce / Loreto Gesualdo

    International Journal of Molecular Sciences, Vol 21, Iss 1, p

    The Missing Link

    2019  Band 189

    Abstract: IgA Nephropathy (IgAN) is a primary glomerulonephritis problem worldwide that develops mainly in the 2nd and 3rd decade of life and reaches end-stage kidney disease after 20 years from the biopsy-proven diagnosis, implying a great socio-economic burden. ... ...

    Abstract IgA Nephropathy (IgAN) is a primary glomerulonephritis problem worldwide that develops mainly in the 2nd and 3rd decade of life and reaches end-stage kidney disease after 20 years from the biopsy-proven diagnosis, implying a great socio-economic burden. IgAN may occur in a sporadic or familial form. Studies on familial IgAN have shown that 66% of asymptomatic relatives carry immunological defects such as high IgA serum levels, abnormal spontaneous in vitro production of IgA from peripheral blood mononuclear cells (PBMCs), high serum levels of aberrantly glycosylated IgA1, and an altered PBMC cytokine production profile. Recent findings led us to focus our attention on a new perspective to study the pathogenesis of this disease, and new studies showed the involvement of factors driven by environment, lifestyle or diet that could affect the disease. In this review, we describe the results of studies carried out in IgAN patients derived from genomic and epigenomic studies. Moreover, we discuss the role of the microbiome in the disease. Finally, we suggest a new vision to consider IgA Nephropathy as a disease that is not disconnected from the environment in which we live but influenced, in addition to the genetic background, also by other environmental and behavioral factors that could be useful for developing precision nephrology and personalized therapy.
    Schlagwörter iga nephropathy ; microbiome ; virome ; environment ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2019-12-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  6. Artikel ; Online: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles

    Rossana Franzin / Alessandra Stasi / Giuseppe De Palma / Angela Picerno / Claudia Curci / Serena Sebastiano / Monica Campioni / Antonella Cicirelli / Alessandro Rizzo / Vito Francesco Di Lorenzo / Paola Pontrelli / Giovanni Battista Pertosa / Giuseppe Castellano / Loreto Gesualdo / Fabio Sallustio

    Cells, Vol 12, Iss 1655, p

    2023  Band 1655

    Abstract: Cisplatin is one of the most effective chemotherapeutic agents strongly associated with nephrotoxicity. Tubular adult renal progenitor cells (tARPC) can regenerate functional tubules and participate in the repair processes after cisplatin exposition. ... ...

    Abstract Cisplatin is one of the most effective chemotherapeutic agents strongly associated with nephrotoxicity. Tubular adult renal progenitor cells (tARPC) can regenerate functional tubules and participate in the repair processes after cisplatin exposition. This study investigated the molecular mechanisms underlying the protective effect of tARPC on renal epithelium during cisplatin nephrotoxicity. By performing a whole-genome transcriptomic analysis, we found that tARPC, in presence of cisplatin, can strongly influence the gene expression of renal proximal tubular cell [RPTEC] by inducing overexpression of CYP1B1, a member of the cytochrome P450 superfamily capable of metabolizing cisplatin and of hypoxia/cancer-related lncRNAs as MIR210HG and LINC00511. Particularly, tARPC exerted renoprotection and regeneration effects via extracellular vesicles (EV) enriched with CYP1B1 and miR-27b-3p, a well-known CYP1B1 regulatory miRNA. The expression of CYP1B1 by tARPC was confirmed by analyzing biopsies of cisplatin-treated renal carcinoma patients that showed the colocalization of CYP1B1 with the tARPC marker CD133. CYP1B1 was also overexpressed in urinary EV purified from oncologic patients that presented nephrotoxicity episodes after cisplatin treatment. Interestingly CYP1B1 expression significantly correlated with creatinine and eGFR levels. Taken together, our results show that tARPC are able to counteract cisplatin-induced nephrotoxicity via CYP1B1 release through EV. These findings provide a promising therapeutic strategy for nephrotoxicity risk assessment that could be related to abundance of renal progenitors.
    Schlagwörter cisplatin-induced AKI ; onconephrology ; regenerative medicine ; tubular adult renal progenitor cells ; extracellular vesicles ; CYP1B1 ; Biology (General) ; QH301-705.5
    Thema/Rubrik (Code) 616
    Sprache Englisch
    Erscheinungsdatum 2023-06-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  7. Artikel ; Online: Potential Reparative Role of Resident Adult Renal Stem/Progenitor Cells in Acute Kidney Injury

    Fabio Sallustio / Grazia Serino / Francesco Paolo Schena

    BioResearch Open Access, Vol 4, Iss 1, Pp 326-

    2015  Band 333

    Abstract: Human kidney is particularly susceptible to ischemia and toxins with consequential tubular necrosis and activation of inflammatory processes. This process can lead to the acute renal injury, and even if the kidney has a great capacity for regeneration ... ...

    Abstract Human kidney is particularly susceptible to ischemia and toxins with consequential tubular necrosis and activation of inflammatory processes. This process can lead to the acute renal injury, and even if the kidney has a great capacity for regeneration after tubular damage, in several circumstances, the normal renal repair program may not be sufficient to achieve a successful regeneration. Resident adult renal stem/progenitor cells could participate in this repair process and have the potentiality to enhance the renal regenerative mechanism. This could be achieved both directly, by means of their capacity to differentiate and integrate into the renal tissues, and by means of paracrine factors able to induce or improve the renal repair or regeneration. Recent genetic fate-tracing studies indicated that tubular damage is instead repaired by proliferative duplication of epithelial cells, acquiring a transient progenitor phenotype and by fate-restricted clonal cell progeny emerging from different nephron segments. In this review, we discuss about the properties and the reparative characteristics of high regenerative CD133+/CD24+ cells, with a view to a future application of these cells for the treatment of acute renal injury.
    Schlagwörter renal progenitor cells ; acute kidney injury ; regenerative medicine ; toll-like receptors ; Medicine ; R ; Biology (General) ; QH301-705.5
    Thema/Rubrik (Code) 616
    Sprache Englisch
    Erscheinungsdatum 2015-07-01T00:00:00Z
    Verlag Mary Ann Liebert
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  8. Artikel ; Online: Beneficial effects of recombinant CER-001 high-density lipoprotein infusion in sepsis

    Alessandra Stasi / Marco Fiorentino / Rossana Franzin / Francesco Staffieri / Sabrina Carparelli / Rosa Losapio / Alberto Crovace / Luca Lacitignola / Maria Teresa Cimmarusti / Francesco Murgolo / Monica Stufano / Cesira Cafiero / Giuseppe Castellano / Fabio Sallustio / Chiara Ferrari / Mario Ribezzi / Nicola Brienza / Annalisa Schirinzi / Francesca Di Serio /
    Salvatore Grasso / Paola Pontrelli / Cyrille Tupin / Ronald Barbaras / Constance Keyserling-Peyrottes / Antonio Crovace / Loreto Gesualdo

    BMC Medicine, Vol 21, Iss 1, Pp 1-

    results from a bench to bedside translational research project

    2023  Band 18

    Abstract: Abstract Background Sepsis is characterized by a dysregulated immune response and metabolic alterations, including decreased high-density lipoprotein cholesterol (HDL-C) levels. HDL exhibits beneficial properties, such as lipopolysaccharides (LPS) ... ...

    Abstract Abstract Background Sepsis is characterized by a dysregulated immune response and metabolic alterations, including decreased high-density lipoprotein cholesterol (HDL-C) levels. HDL exhibits beneficial properties, such as lipopolysaccharides (LPS) scavenging, exerting anti-inflammatory effects and providing endothelial protection. We investigated the effects of CER-001, an engineered HDL-mimetic, in a swine model of LPS-induced acute kidney injury (AKI) and a Phase 2a clinical trial, aiming to better understand its molecular basis in systemic inflammation and renal function. Methods We carried out a translational approach to study the effects of HDL administration on sepsis. Sterile systemic inflammation was induced in pigs by LPS infusion. Animals were randomized into LPS (n = 6), CER20 (single dose of CER-001 20 mg/kg; n = 6), and CER20 × 2 (two doses of CER-001 20 mg/kg; n = 6) groups. Survival rate, endothelial dysfunction biomarkers, pro-inflammatory mediators, LPS, and apolipoprotein A-I (ApoA-I) levels were assessed. Renal and liver histology and biochemistry were analyzed. Subsequently, we performed an open-label, randomized, dose-ranging (Phase 2a) study included 20 patients with sepsis due to intra-abdominal infection or urosepsis, randomized into Group A (conventional treatment, n = 5), Group B (CER-001 5 mg/kg BID, n = 5), Group C (CER-001 10 mg/kg BID, n = 5), and Group D (CER-001 20 mg/kg BID, n = 5). Primary outcomes were safety and efficacy in preventing AKI onset and severity; secondary outcomes include changes in inflammatory and endothelial dysfunction markers. Results CER-001 increased median survival, reduced inflammatory mediators, complement activation, and endothelial dysfunction in endotoxemic pigs. It enhanced LPS elimination through the bile and preserved liver and renal parenchyma. In the clinical study, CER-001 was well-tolerated with no serious adverse events related to study treatment. Rapid ApoA-I normalization was associated with enhanced LPS removal and immunomodulation with ...
    Schlagwörter ApoA-I complexes ; Sepsis ; Multi-organ dysfunction ; Cytokine storm ; Medicine ; R
    Thema/Rubrik (Code) 616
    Sprache Englisch
    Erscheinungsdatum 2023-11-01T00:00:00Z
    Verlag BMC
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  9. Artikel ; Online: Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics

    Stefano Battaglia / Stefania De Santis / Monica Rutigliano / Fabio Sallustio / Angela Picerno / Maria Antonia Frassanito / Ingo Schaefer / Angelo Vacca / Antonio Moschetta / Peter Seibel / Michele Battaglia / Gaetano Villani

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    a clinical pilot study

    2021  Band 9

    Abstract: Abstract Antibiotics that inhibit bacterial protein or nucleic acid synthesis and function can exert an off-target action on mitochondria (mitotoxic antibiotics), making actively dividing mammalian cells dependent on uridine and pyruvate supplementation. ...

    Abstract Abstract Antibiotics that inhibit bacterial protein or nucleic acid synthesis and function can exert an off-target action on mitochondria (mitotoxic antibiotics), making actively dividing mammalian cells dependent on uridine and pyruvate supplementation. Based on this rationale, we carried out, for the first time, a randomized pilot study in 55 patients with asymptomatic bacteriuria or positive sperm culture, each treated with a single mitotoxic antibiotic with or without oral supplementation of uridine + pyruvate (Uripyr, Mitobiotix, Italy). The in vivo and ex vivo data show a a 3.4-fold higher value in the differential (before and after the antibiotic treatment) lymphocytes count and a 3.7-fold increase in the percentage of dividing T cells, respectively, in the Uripyr vs the control group. Our findings lay the groundwork to enhance the synergy between antibiotics and the immune system in order to optimize the administration protocols and widen the application potentials of antibiotic therapies as well as to re-evaluate old “forgotten” molecules to fight bacterial infections in the antibiotics resistance era.
    Schlagwörter Medicine ; R ; Science ; Q
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2021-06-01T00:00:00Z
    Verlag Nature Portfolio
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

  10. Artikel ; Online: Rifaximin as a Potential Treatment for IgA Nephropathy in a Humanized Mice Model

    Vincenzo Di Leo / Patrick J. Gleeson / Fabio Sallustio / Carine Bounaix / Jennifer Da Silva / Gesualdo Loreto / Sanae Ben Mkaddem / Renato C. Monteiro

    Journal of Personalized Medicine, Vol 11, Iss 309, p

    2021  Band 309

    Abstract: IgA Nephropathy (IgAN) is the most common glomerulonephritis worldwide, characterized by the mesangial deposition of abnormally glycosylated IgA1 (Gd-IgA). The production of Gd-IgA occurs in mucose-associated lymphoid tissue (MALT). The microbiota plays ... ...

    Abstract IgA Nephropathy (IgAN) is the most common glomerulonephritis worldwide, characterized by the mesangial deposition of abnormally glycosylated IgA1 (Gd-IgA). The production of Gd-IgA occurs in mucose-associated lymphoid tissue (MALT). The microbiota plays a role in MALT modulation. Rifaximin (NORMIX ® ), a non-absorbable oral antibiotic, induces positive modulation of the gut microbiota, favoring the growth of bacteria beneficial to the host. Here, we evaluate the effect of rifaximin on a humanized mice model of IgAN (α1 KI -CD89 Tg ). Methods: The α1 KI -CD89 Tg mice were treated by the vehicle (olive oil) or rifaximin (NORMIX ® ). Serum levels of hIgA, hIgA1–sCD89, and mIgG–hIgA1 immune complexes were determined. Glomerular hIgA1 deposit and CD11b+ cells recruitment were revealed using confocal microscopy. Furthermore, the mRNA of the B-Cell Activating Factor (BAFF), polymeric immunoglobulin receptor (pIgR), and Tumor Necrosing Factor-α (TNF-α) in gut samples were detected by qPCR. Results: Rifaximin treatment decreased the urinary protein-to-creatinine ratio, serum levels of hIgA1–sCD89 and mIgG–hIgA1 complexes, hIgA1 glomerular deposition, and CD11b+ cell infiltration. Moreover, rifaximin treatment decreased significantly BAFF, pIgR, and TNF-α mRNA expression. Conclusions: Rifaximin decreased the IgAN symptoms observed in α1 KI -CD89 Tg mice, suggesting a possible role for it in the treatment of the disease.
    Schlagwörter IgA Nephropathy ; rifaximin ; microbiota ; α1 KI -CD89 Tg mice ; Medicine ; R
    Sprache Englisch
    Erscheinungsdatum 2021-04-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

    Zusatzmaterialien

    Kategorien

Zum Seitenanfang