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Dive into the research topics where Maria Laura Uzzo is active.

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Featured researches published by Maria Laura Uzzo.


Folia Histochemica Et Cytobiologica | 2012

Immunohistochemical expression and distribution of orexin, orphanin and leptin in the major salivary glands of some mammals

Angelo Leone; Giovanni Francesco Spatola; Daniela Cucco; Vincenzo Tessitore; Giuseppe Bonaventura; Maria Laura Uzzo

The aim of the study was to determine by immunochemistry the expression of leptin, orexin A and orphanin FQ in the major salivary glands (parotid, submandibular and sublingual) of rat, sheep and cow. These peptides, originally synthesized in central nervous system, adipose tissue and peripheral tissues including gastrointestinal tract, play an orexigenic (orphanin and orexin) or anorexigenic (leptin) roles in the intricate neuronal network appointed to the control of nutritional homeostasis. Peptide-specific immunoreactivity was present in the studied salivary glands with various intensities in different species, in the ductal epithelium, sometimes in the acinar epithelium, and in nervous trunks spread in connective tissue stroma. The obtained data show that salivary glands present an unexpected source of orexigenic and anorexigenic peptides which with their autocrine, paracrine, and endocrine mechanisms of action may participate in the control of salivary gland function.


International Journal of Immunopathology and Pharmacology | 2014

Modulation of MMP-2 and MMP-9 in Churg-Strauss syndrome respiratory mucosa: potential monitoring parameters

Angelo Leone; Maria Laura Uzzo; Aldo Gerbino; Silvia Tortorici; Tralongo P; Francesco Cappello; S Incandela; Giovanni Francesco Spatola; Abdo Jurjus

Churg-Strauss (CSS) syndrome is rare and of unknown etiology. It is associated with vasculitis, blood eosinophilia and granulomatosis, and affects multiple organs and systems at various stages of the disease. Specific diagnostic and monitoring tests are not yet available. This study aims to assess the changes in MMP-2 and MMP-9 along with the histopathological alterations in two cases of CSS, as possible potential diagnostic and monitoring criteria. Two adult male patients were diagnosed with CSS in the otorhinolaryngology clinic in the University of Palermo, based on multiple clinical and histopathologic criteria. Biopsies of respiratory mucosa were taken after the consent of the patients, processed for routine histopathology and immunohistochemistry as well as quantitative polymerase chain reaction (qPCR). Similar biopsies were also taken from a non-CSS patient. The Assessment of MMP-2 and MMP-9 was performed using both immunohistochemistry and qPCR techniques. Histopathological alterations in the respiratory mucosa were consistent with vasculitis and granulomatous tissue formation, in addition to inflammatory cell infiltration with abundance of eosinophils. Immunohistochemistry assay performed on the samples derived from the two CSS patients showed a relative and remarkable increase of both MMP-2 and MMP-9 compared to controls. Such an increase was consistent with the qPCR results which depicted a significant increase between 20 and 30% for both MMP-2 and MMP-9, respectively. Since the secretion of MMPs is an essential step in angiogenesis, could these enzymatic factors be used as parameters to diagnose or monitor the evolution of CSS? The small number of samples analyzed in this study does not allow us to suggest a general statement correlating the increase in expression of MMP-2 and MMP-9 to the appearance or evolution of vasculitis; it is only speculative.


Folia Histochemica Et Cytobiologica | 2012

Immunohistochemical expression of apoptotic factors, cytokeratins, and metalloproteinase-9 in periapical and epithelialized gingival lesions

Angelo Leone; Maria Laura Uzzo; Francesca Rappa; Inaya Hajj Hussein; Aldo Gerbino; Giovanni Francesco Spatola; Abdo Jurjus

Bellmann K, 2010, CELL STRESS CHAPERON, V15, P101, DOI 10.1007-s12192-009-0126-9; Cappello Francesco, 2011, Front Biosci (Schol Ed), V3, P341, DOI 10.2741-s155; Cappello F, 2006, CANCER, V107, P2417, DOI 10.1002-cncr.22265; Cappello F, 2002, EUR J HISTOCHEM, V46, P199; Carneiro E, 2009, ORAL SURG ORAL MED O, V107, P127, DOI 10.1016-j.tripleo.2008.07.030; Chandra D, 2007, J BIOL CHEM, V282, P31289, DOI 10.1074-jbc.M702777200; Fujita Y, 2011, ODONTOLOGY, V100, P215; Garcia Celia Carrillo, 2007, Med Oral Patol Oral Cir Bucal, V12, pE585; Garcia CC, 2009, ORAL SURG ORAL MED O, V107, pE43, DOI 10.1016-j.tripleo.2008.12.002; Gregory CD, 2011, J PATHOL, V223, P177, DOI 10.1002-path.2792; Gupta S, 2002, CIRCULATION, V106, P2727, DOI 10.1061-01.CIR.0000038112.64503.6E; Hajra KM, 2004, APOPTOSIS, V9, P691, DOI 10.1023-B:APPT.0000045786.98031.1d; Kimi K, 2001, J ORAL PATHOL MED, V30, P434, DOI 10.1034-j.1600-0714.2001.300709.x; Kirkeby S, 2005, J IMMUNOL METHODS, V301, P102, DOI 10.1016-j.jim.2005.04.006; Lehr HA, 1997, J HISTOCHEM CYTOCHEM, V45, P1559; Leonardi R, 2003, J ENDODONT, V29, P180, DOI 10.1097-00004770-200303000-00004; Li P, 1997, CELL, V91, P479, DOI 10.1016-S0092-8674(00)80434-1; Mak BC, 2008, J BIOL CHEM, V283, P23462, DOI 10.1074-jbc.M803194200; Martins CA, 2011, J ENDODONT, V37, P36, DOI 10.1016-j.joen.2010.09.010; MARTON IJ, 1993, INT ENDOD J, V26, P131, DOI 10.1111-j.1365-2591.1993.tb00555.x; MOLL R, 1982, CELL, V31, P11, DOI 10.1016-0092-8674(82)90400-7; Nagata S, 1999, ANNU REV GENET, V33, P29, DOI 10.1146-annurev.genet.33.1.29; Pham NA, 2007, DIAGN PATHOL, V27, P2; Pritlove-Carson S, 1997, Oral Dis, V3, P19; Samali A, 1999, EMBO J, V18, P2040, DOI 10.1093-emboj-18.8.2040; Sawaf M H, 1991, J Biol Buccale, V19, P187; Skaland I, 2008, J CLIN PATHOL, V61, P68, DOI 10.1136-jcp.2007.046763; Skaland I, 2008, APPL IMMUNOHISTO M M, V16, P185, DOI 10.1097-PAI.0b013e318059c20c; Suzuki T, 2005, J ORAL PATHOL MED, V34, P46, DOI 10.1111-j.1600-0714.2004.00248.x; Suzuki T, 2002, J ORAL PATHOL MED, V31, P488, DOI 10.1034-j.1600-0714.2002.00016.x; Taylor CR, 2006, HISTOPATHOLOGY, V49, P411, DOI 10.1111-j.1365-2559.2006.02513.x; Tuan RS, 2011, INT J ORAL MAX IMPL, V26, P50; Tuan RS, 2011, INT J ORAL MAX SURG, V26, P63; Walker RA, 2006, HISTOPATHOLOGY, V49, P406, DOI 10.1111-j.1365-2559.2006.02514.x; Xanthoudakis S, 1999, EMBO J, V18, P2049, DOI 10.1093-emboj-18.8.2049


Anatomia Histologia Embryologia | 2009

Immunohistochemical and biomolecular identification of orphanin FQ, eNOS, atrial natriuretic factor and oxytocin in rat seminal vesicles.

A. Mauro; Maria Buscemi; Francesco Cappello; Maria Laura Uzzo; Farina-Lipari E; Martorana A; Aldo Gerbino

In previous studies performed on rodents, we detected the presence of adreno‐cholinergic and peptidergic innervation in seminal vesicles and other organs of the male genital system, such as prostate and deferent duct, in which we also investigated the expression of NOS and NADPH‐diaphorase. During this project, we focused our attention on the expression of some peptides involved in local control of smooth muscle relaxation, contractility, vasodilatation and control of blood flow in rat seminal vesicles. We investigated, through immunohistochemistry and RT‐PCR, the presence of four peptides: orphanin, eNOS, ANF and oxytocin. Immunohistochemistry was used to detect the presence of the proteins, whereas RT‐PCR analysis confirmed gene expression of orphanin, eNOS and ANF, but not oxytocin. In our opinion, orphanin, eNOS and ANF could have paracrine effects regulating the function of seminal vesicles, whereas oxytocin, which may reach this anatomical district through the blood flow, may have a hormonal action. This is a pilot study that, with further investigation, may allow to better clarify the role of these molecules in the control of seminal vesicle tissues’ homeostasis.


Italian journal of anatomy and embryology | 2011

Immunohistochemical expression of Cytokeratins in periapical lesions

Angelo Leone; Maria Laura Uzzo; Giovanni Francesco Spatola; Aldo Gerbino; Giuseppe Bonaventura

Objective. This study seeks to clarify the histological origin of apical lesions, through the expression of certain cytokeratins.Study design. In 3 years 30 patients were selected. After clinical and radiological exams were chosen patients who had severe apical lesions and tooth decay with exposure of the pulp chamber left untreated for very long periods (more the 12 months). Serial slides were prepared both for immunohistochemistry and Hematoxylin- Eosin. Material and methods. Twenty specimens coming from the 30 patients were used for our purpose. All periapical lesions were surgically extracted and fixed in Bouin mixture, and embedded in paraffin. Samples were processed immunohistochemically employing the instructions of the Envision Dako cytomation kit. Monoclonal antibobies against Cytokeratins (CKs) 1, 5 , 8, 10 and 14 were used. Slides were observed with Leica Laborlux-S microscope and the image were acquired with NIKON DSL2 System. Each sample has been analyzed with a “double-blind” system by two different operators. Moreover, the digital images acquired have been compared to an image analysis tools by Adobe photoshop CS5 Extended. Results. CKs 1, 5 and 8 are expressed in all samples at external epithelial layer with no statistically significant differences. CK 10 is weakly expressed in some epithelial cells lining the periapical lesion. CK 14 was negative in most samples, and little positive in some specimens. Conclusion. Our results suggest that most of the apical lesions we studied have an epithelial origin. The absence of CK14 positivity may be explained by the fact that during the extirpation of the lesion the basal epithelium remained attached to the surrounding bone.


Journal of Biological Regulators and Homeostatic Agents | 2014

Lactobacillus casei and bifidobacterium lactis supplementation reduces tissue damage of intestinal mucosa and liver after 2,4,6-trinitrobenzenesulfonic acid treatment in mice.

Aldo Gerbino; Giovanni Zummo; Felicia Farina; Giuseppe Bonaventura; Angelo Leone; Francesco Cappello; Giovanni Tomasello; Maria Laura Uzzo; Giovanni Francesco Spatola; Sabrina David; Francesca Rappa; Margherita Lo Bello; Provvidenza Damiani; Schembri-Wismayer; Jurjus; Giovanna Traina; Brecchia; Maurizio Bellavia; Hajj-Hussein; Zeenny; Massimo Cocchi


Anticancer Research | 2014

Comparative analysis of Hsp10 and Hsp90 expression in healthy mucosa and adenocarcinoma of the large bowel.

F. Rappa; Carmelo Sciume; Lo Bello M; Celeste Caruso Bavisotto; Marino Gammazza A; Rosario Barone; Claudia Campanella; Sabrina David; Francesco Carini; Zarcone F; Rizzuto S; Adriana Lena; Giovanni Tomasello; Maria Laura Uzzo; Giovanni Francesco Spatola; Giuseppe Bonaventura; Angelo Leone; Aldo Gerbino; Francesco Cappello; Fabio Bucchieri; Giovanni Zummo; Felicia Farina


Acta Otorhinolaryngologica Italica | 2015

The immunohistochemical peptidergic expression of leptin is associated with recurrence of malignancy in laryngeal squamous cell carcinoma.

S. Gallina; F. Sireci; F. loruSSo; D.V. Di Benedetto; R. Speciale; D. Marchese; Claudio Costantino; Giuseppe Napoli; Vincenzo Tessitore; D Cucco; Angelo Leone; Giuseppe Bonaventura; Maria Laura Uzzo; Giovanni Francesco Spatola


Journal of Biological Regulators and Homeostatic Agents | 2013

Orthodontic stress Bcl-2 modulation and human odontoblast survival.

Angelo Leone; Luana Lipari; Maria Laura Uzzo; Giovanni Francesco Spatola; S Provenzano; Aldo Gerbino; Abdo Jurjus


Bulletin du Groupement International pour la Recherche Scientifique en Stomatologie et Odontologie | 2008

Expression and modification of NO synthase in human dental pulps during orthodontic treatment.

Angelo Leone; M Patel; Maria Laura Uzzo; Maria Buscemi; Aldo Gerbino

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Abdo Jurjus

American University of Beirut

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