Roberta Ceci

Dr. Roberta Ceci

Unit of Biochemistry and Molecular Biology, Department of Movement, Human and Health Sciences, University of Rome FORO ITALICO, Piazza Lauro de Bosis 6, 00135 Rome, Italy
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Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 1998 in Journal of Investigative Dermatology
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Journal Article
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ARAntonello Rossi
Antonello Rossi
SJShyh-Ing Jang
Shyh-Ing Jang
Roberta CeciRoberta Ceci
Roberta Ceci
PSPeter M. Steinert
Peter M. Steinert
NMNedialka G. Markova
Nedialka G. Markova

14 February 2014 in Cellular and Molecular Life Sciences
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Journal Article
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MTMirko Tantimonaco
Mirko Tantimonaco
Roberta CeciRoberta Ceci
Roberta Ceci
SSStefania Sabatini
Stefania Sabatini
MCMaria Valeria Catani
Maria Valeria Catani
ARAntonello Rossi
Antonello Rossi
Mauro MaccarroneMauro Maccarrone
Mauro Maccarrone

31 May 2021 in Nutrients
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Journal Article
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BDBarbara Dorelli
Barbara Dorelli
Francesca GallèFrancesca Gallè
Francesca Gallè
CVCorrado De Vito
Corrado De Vito
Guglielmo DurantiGuglielmo Duranti
Guglielmo Duranti
MIMatteo Iachini
Matteo Iachini
MCMaria Sofia Cattaruzza
Maria Sofia Cattaruzza
Evidence suggests that physical activity (PA) influences the human gut microbiota composition, but its role is unclear because of dietary interference. The aim of this review is to clarify this issue from this new perspective in healthy individuals. Articles analyzing intestinal microbiota from fecal samples by 16S rRNA amplicon sequencing were selected by searching the electronic databases PubMed, Scopus, and Web of Science until December 2020. For each study, methodological quality was assessed, and results about microbiota biodiversity indices, phylum and genus composition, and information on PA and diet were considered. From 997 potentially relevant articles, 10 met the inclusion criteria and were analyzed. Five studies involved athletes, three were performed on active people classified on the basis of habitual PA level, and two among sedentary subjects undergoing exercise interventions. The majority of the studies reported higher variability and prevalence of the phylum Firmicutes (genera Ruminococcaceae or Fecalibacteria) in active compared to inactive individuals, especially in athletes. The assessment of diet as a possible confounder of PA/exercise effects was completed only in four studies. They reported a similar abundance of Lachnospiraceae, Paraprevotellaceae, Ruminococcaceae, and Veillonellaceae, which are involved in metabolic, protective, structural, and histological functions. Further studies are needed to confirm these findings.

1 October 2004 in Free Radical Biology and Medicine
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Journal Article
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MCM. Valeria Catani
M. Valeria Catani
ISIsabella Savini
Isabella Savini
Guglielmo DurantiGuglielmo Duranti
Guglielmo Duranti
DCDaniela Caporossi
Daniela Caporossi
Roberta CeciRoberta Ceci
Roberta Ceci
LALuciana Avigliano
Luciana Avigliano

1 May 1998 in Journal of Biological Chemistry
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ECEleonora Candi
Eleonora Candi
GMGerry Melino
Gerry Melino
ALArmin Lahm
Armin Lahm
Roberta CeciRoberta Ceci
Roberta Ceci
ARAntonello Rossi
Antonello Rossi
PSPeter M. Steinert
Peter M. Steinert
Lamellar ichthyosis is a congenital recessive skin disorder characterized by generalized scaling and hyperkeratosis. It is caused by mutations in the TGM1gene that encodes the transglutaminase 1 (TGase 1) enzyme, which is critical for the assembly of the cornified cell envelope in terminally differentiating keratinocytes. TGase 1 is a complex enzyme existing as both cytosolic and membrane-bound forms. Moreover, TGase 1 is proteolytically processed, and the major functionally active form consists of a membrane-bound 67/33/10-kDa complex with a myristoylated and palmitoylated amino-terminal 10-kDa membrane anchorage fragment. To understand better how point mutations, deletions, and truncations found in lamellar ichthyosis disease affect the structure and function of TGase 1, we have expressed in baculovirus and keratinocytes a number of reported TGase 1 mutants. The structural implications of these mutations were examined using a homology-derived three-dimensional model of TGase 1 generated from the known x-ray structure of the related coagulation factor XIIIa enzyme. The present studies demonstrate that loss of TGase 1 activity is not restricted to mutations that directly affect the enzymatic activity. We report a new class of mutations that impair the subsequent post-synthetic processing of the protein into its highly active functional forms.

1 January 2014 in Redox Biology
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Journal Article
Open access
Roberta CeciRoberta Ceci
Roberta Ceci
MVMaria Reyes Beltran Valls
Maria Reyes Beltran Valls
Guglielmo DurantiGuglielmo Duranti
Guglielmo Duranti
Ivan DimauroIvan Dimauro
Ivan Dimauro
FQFederico Quaranta
Federico Quaranta
DCDaniela Caporossi
Daniela Caporossi
We recently demonstrated that low frequency, moderate intensity, explosive-type resistance training (EMRT) is highly beneficial in elderly subjects towards muscle strength and power, with a systemic adaptive response of anti-oxidant and stress-induced markers. In the present study, we aimed to evaluate the impact of EMRT on oxidative stress biomarkers induced in old people (70-75 years) by a single bout of acute, intense exercise. Sixteen subjects randomly assigned to either a control, not exercising group (n=8) or a trained group performing EMRT protocol for 12-weeks (n=8), were submitted to a graded maximal exercise stress test (GXT) at baseline and after the 12-weeks of EMRT protocol, with blood samples collected before, immediately after, 1 and 24h post-GXT test. Blood glutathione (GSH, GSSG, GSH/GSSG), plasma malonaldehyde (MDA), protein carbonyls and creatine kinase (CK) levels, as well as PBMCs cellular damage (Comet assay, apoptosis) and stress-protein response (Hsp70 and Hsp27 expression) were evaluated. The use of multiple biomarkers allowed us to confirm that EMRT per se neither affected redox homeostasis nor induced any cellular and oxidative damage. Following the GXT, the EMRT group displayed a higher GSH/GSSG ratio and a less pronounced increase in MDA, protein carbonyls and CK levels compared to control group. Moreover, we found that Hsp70 and Hsp27 proteins were induced after GXT only in EMRT group, while any significant modification within 24h was detected in untrained group. Apoptosis rates and DNA damage did not show any significant variation in relation to EMRT and/or GXT. In conclusion, the adherence to an EMRT protocol is able to induce a cellular adaptation allowing healthy elderly trained subjects to cope with the oxidative stress induced by an acute exercise more effectively than the aged-matched sedentary subjects.