Rodolfo Lorenzini
Istituto Superiore di Sanità
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Featured researches published by Rodolfo Lorenzini.
Journal of Experimental Medicine | 2003
Anna Rita Migliaccio; Rosa Alba Rana; Massimo Sanchez; Rodolfo Lorenzini; Lucia Centurione; Lucia Bianchi; Alessandro M. Vannucchi; Giovanni Migliaccio; Stuart H. Orkin
Here it is shown that the phenotype of adult mice lacking the first enhancer (DNA hypersensitive site I) and the distal promoter of the GATA-1 gene (neoΔHS or GATA-1low mutants) reveals defects in mast cell development. These include the presence of morphologically abnormal alcian blue+ mast cells and apoptotic metachromatic− mast cell precursors in connective tissues and peritoneal lavage and numerous (60–70% of all the progenitors) “unique” trilineage cells committed to erythroid, megakaryocytic, and mast pathways in the bone marrow and spleen. These abnormalities, which were mirrored by impaired mast differentiation in vitro, were reversed by retroviral-mediated expression of GATA-1 cDNA. These data indicate an essential role for GATA-1 in mast cell differentiation.
Oncogene | 2003
Rosamaria Mangiacasale; Carmine Pittoggi; Ilaria Sciamanna; Angela Careddu; Elisabetta Mattei; Rodolfo Lorenzini; Lorena Travaglini; Matteo Landriscina; Carlo Barone; Clara Nervi; Patrizia Lavia; Corrado Spadafora
Endogenous, nontelomeric reverse transcriptase (RT) is encoded by two classes of repeated elements: retrotransposons and endogenous retroviruses. Expression of RT-coding genes is generally repressed in differentiated nonpathological tissues, yet is active in the mammalian germ line, embryonic tissues and tumor cells. Nevirapine is a non-nucleoside RT inhibitor with a well-characterized inhibitory activity on RT enzymes of retroviral origin. Here, we show that nevirapine is also an effective inhibitor of the endogenous RT in murine and human cell lines. In addition, progenitor and transformed cells undergo a significant reduction in the rate of cell growth upon exposure to nevirapine. This is accompanied by the onset of differentiation, as depicted in F9 and C2C7 progenitor cells cultures in which nevirapine triggers the expression of differentiation-specific markers. Consistent with this, an extensive reprogramming of cell cycle gene expression was depicted in nevirapine-treated F9 cultures. Furthermore, nevirapine exposure rescued the differentiation block present in acute myeloid leukemia (AML) cell lines and primary blasts from two AML patients, as indicated by morphological, functional and immunophenotypic assays. The finding that an RT inhibitor can modulate cell proliferation and differentiation suggests that RT may represent a novel target in the development of therapeutical approaches to neoplasia.
Mycopathologia | 1986
L. Polonelli; Rodolfo Lorenzini; Flavia De Bernardis; Giulia Morace
Experimental infections were produced in guinea pigs, rabbits and dogs with lesions similar to those seen in human seborrheic dermatitis and otitis externa by cutaneous application of cultures of Malassezia furfur and M. pachydermatis. Infected animals were treated by topical application of a concentrated yeast killer toxin (Hansenula anomala UCSC 25F). Clinical recovery as well as negative mycological test cultures of infected animals proved to the clearly associated with the treatment by the killer toxin.
Molecular Reproduction and Development | 2000
Ilaria Sciamanna; Simona Piccoli; Laura Barberi; Germana Zaccagnini; Anna Rosa Magnano; Roberto Giordano; Paolo Campedelli; Clague P. Hodgson; Rodolfo Lorenzini; Corrado Spadafora
We have tested three parameters in sperm‐mediated gene transfer assays with mice and pigs: (i) the epididymal versus ejaculated origin of sperm cells, (ii) the primary structure, and (iii) the amount of the challenging foreign DNA. We have found that the pVLCNhGH construct, of retrotransposon origin, causes a massive embryo lethality and yet increases the yield of genetic transformation among born animals of both species compared to viral constructs. Arrest of embryonic development is a DNA dose‐dependent effect, which is observed with high DNA doses, while lower doses are compatible with development. Finally, the overall efficiency of sperm‐mediated gene transfer is higher when ejaculated, versus epididymal, spermatozoa are used. We suggest that this difference is related to the highly efficient apoptotic response in epididymal compared to ejaculated spermatozoa, triggered by the interaction of exogenous DNA molecules with the sperm membrane. Mol. Reprod. Dev. 56:301–305, 2000.
Molecular Reproduction and Development | 2000
Carmine Pittoggi; Germana Zaccagnini; Roberto Giordano; Anna Rosa Magnano; Baccio Baccetti; Rodolfo Lorenzini; Corrado Spadafora
Exogenous DNA molecules are spontaneously taken up by sperm cells, internalized in nuclei, and eventually integrated in the sperm genome. The actual occurrence of the integration suggests that the sperm chromosomal DNA is not uniformly and tightly packed with protamines, implying the existence of genomic sites where the chromosomal DNA is accessible to foreign molecules. We have characterized a hypersensitive, nucleosomal subfraction of mouse sperm chromatin that is highly enriched in unmethylated retroposon DNA from a variety of families. Here we propose that both the integration of exogenous DNA molecules, and the endogenous retroposition activity, occur in the same site(s) of sperm chromatin. Mol. Reprod. Dev. 56:248–251, 2000.
Medical Mycology | 1990
F. De Bernardis; Luisella Morelli; T. Ceddia; Rodolfo Lorenzini; Antonio Cassone
Isolates of Candida parapsilosis from women with or without candidal vaginitis were compared for their ability to produce secretory aspartate (acid) proteinase and their virulence for normal or cyclophosphamide-immunodepressed mice. Although all isolates were strongly proteolytic in vitro, only those from candidosis-affected subjects were appreciably pathogenic for neutropenic mice. In these animals, organ invasion was monitored after challenge with representative isolates of each category. The number of yeast cells in the kidneys of animals infected with an isolate from a subject without candidal vaginitis was approximately one order of magnitude less than that in mice infected with either one of two isolates from patients with candidal vaginitis. Mice infected with either category of C. parapsilosis isolates developed antibodies against a mannoprotein-rich extract of the cell wall, and these antibodies did not cross-react with a chemically similar preparation from Candida albicans. However, only those animals which had been challenged with one of the isolates from a candidosis subject produced a low level of antibodies, detectable by ELISA, against an acid proteinase of C. parapsilosis. These antibodies cross-reacted with a highly purified enzyme preparation of C. albicans. The data demonstrate differences in the potential virulence of different isolates of C. parapsilosis and suggest that the ability to express the acid proteinase in vivo may be related to differences in pathogenicity.
FEBS Letters | 2001
Rosamaria Mangiacasale; Alessandra Tritarelli; Ilaria Sciamanna; Maria Cannone; Patrizia Lavia; Massimo Barberis; Rodolfo Lorenzini; Enrico Cundari
Human lymphoblastoid cells of normal origin and from genetic instability syndromes, i.e. Fanconi anemia (FA) group C and ataxia telangectasia, were continuously exposed to extremely low frequency magnetic field (ELF‐MF). We report that ELF‐MF, though not perturbing cell cycle progression, increases the rate of cell death in normal cell lines. In contrast, cell death is not affected in cells from genetic instability syndromes; this reflects a specific failure of the apoptotic response. Reintroduction of complementation group C in FA cells re‐established the apoptotic response to ELF‐MF. Thus, genes implicated in genetic instability syndromes are relevant in modulating the response of cells to ELF‐MF.
Handbook of Animal Models of Infection#R##N#Experimental Models in Antimicrobial Chemotherapy | 1999
F. De Bernardis; Rodolfo Lorenzini; Antonio Cassone
Publisher Summary This chapter presents a rat model of Candida vaginal infection. Several strains of rats have been used in this model including Sprague-Dawley, CD, Wistar, and Alderley Park. No specialized housing or feeding is required, and caring is under the ordinary standards for outbred animal care. Rat vaginal infection by Candida is under strict hormonal control. For the infectious challenge, cells of each Candida strain tested are grown in Winge broth for 48 hours at 28° C on a shaker at 200 rpm. Growth is measured by hemocytometer counts and the yeast suspension is appropriately diluted in physiological saline before animal inoculation. Six days after the first estradiol dose, the animals are inoculated intravaginally with Candida cells in 0.1 ml of saline solution, which is administered to each animal through a syringe equipped with a multipurpose calibrated tip. To favor intravaginal contact and adsorption of fungal cells, the rat is held head-down for 1 minute. For immunological studies and detection of antibodies, samples of vaginal fluids are taken at regular intervals from each animal by gently washing the vaginal cavity with 0.5 ml of sterile saline solution. For the histological examination of vaginal tissue, the vaginas from euthanized Candida-infected rats and control are aseptically removed and fixed in 10% (vol/vol) formalin. Paraffin sections are examined after treatment with PAS and van Giesen stains. A major advantage of the rat model is the possibility of obtaining a relatively large amount of vaginal fluid and other materials for the studies of pathogenesis and immunity in candidiasis.
Mutation Research-genetic Toxicology and Environmental Mutagenesis | 2003
Rosanna Beraldi; Ilaria Sciamanna; Rosamaria Mangiacasale; Rodolfo Lorenzini; Corrado Spadafora
We have investigated the sensitivity of pre-implantation embryos obtained by natural breeding (NB) or in vitro fertilization (IVF) to extremely low-frequency magnetic fields (ELF-MF). Fertilized eggs obtained by NB were removed from mothers 12h after mating and cultured in vitro for 5 days under continuous ELF-MF exposure (constant strength of 50Hz and various intensities, i.e. 60, 120 and 220 microT). Alternatively, zygotes obtained by IVF were subjected to ELF-MF exposure (50Hz, 60 microT), starting 12h after IVF for 5 days. We found that ELF-MF exposure causes a small yet significant (P<0.05) decrease in the survival rate of NB-derived embryos at the latest stages of pre-implantation development, i.e. the eight cell-to-blastocyst transition. In embryos exposed to the highest field intensity (220 microT), the effect became apparent somewhat earlier. When IVF-derived embryos were exposed to ELF-MF, the reduction in the rate of embryo survival was more pronounced and the difference from controls was more significant (P<0.01). Moreover, the decreased survival rate in IVF embryos became apparent as early as the first cleavage and persisted throughout pre-implantation. These results suggest that IVF-derived embryos are more sensitive than NB-generated embryos to ELF-MF, and that this sensitivity occurs earlier in development.
Mycopathologia | 1987
Rodolfo Lorenzini; Flavia De Bernardis
Results related to the isolation, cultivation, culture and maintenance of the opportunistic pathogen Malassezia pachydermatis are reported. A dextrose nutrient medium with 1.5% yeast extract turned out to be the most favourable medium for its development. It permitted identification in 24 hours and maintenance of isolates for three months without subculturing. Addition of Tween 80 (1%) significantly enhanced the isolation of this yeast from clinical materials.