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1.
Cell Transplant ; 27(1): 117-129, 2018 01.
Article in English | MEDLINE | ID: mdl-29562783

ABSTRACT

Wharton's jelly mesenchymal stromal cells (WJ-MSCs) have been recently exploited as a feeder layer in coculture systems to expand umbilical cord blood-hematopoietic stem/progenitor cells (UCB-HSPCs). Here, we investigated the role of WJ-MSCs in supporting ex vivo UCB-HSPC expansion either when cultured in direct contact (DC) with WJ-MSCs or separated by a transwell system or in the presence of WJ-MSC-conditioned medium. We found, in short-term culture, a greater degree of expansion of UCB-CD34+ cells in a DC system (15.7 ± 4.1-fold increase) with respect to the other conditions. Moreover, in DC, we evidenced two different CD34+ cell populations (one floating and one adherent to WJ-MSCs) with different phenotypic and functional characteristics. Both multipotent CD34+/CD38- and lineage-committed CD34+/CD38+ hematopoietic progenitors were expanded in a DC system. The former were significantly more represented in the adherent cell fraction than in the floating one (18.7 ± 11.2% vs. 9.7 ± 7.9% over the total CD34+ cells). Short-term colony forming unit (CFU) assays showed that HSPCs adherent to the stromal layer were able to generate a higher frequency of immature colonies (CFU-granulocyte/macrophage and burst-forming unit erythroid/large colonies) with respect to the floating cells. In the attempt to identify molecules that may play a role in supporting the observed ex vivo HSPC growth, we performed secretome analyses. We found a number of proteins involved in the HSPC homing, self-renewal, and differentiation in all tested conditions. It is important to note that a set of sixteen proteins, which are only in part reported to be expressed in any hematopoietic niche, were exclusively found in the DC system secretome. In conclusion, WJ-MSCs allowed a significant ex vivo expansion of multipotent as well as committed HSPCs. This may be relevant for future clinical applications.


Subject(s)
Cell Culture Techniques/methods , Hematopoietic Stem Cells/cytology , Mesenchymal Stem Cells/cytology , Wharton Jelly/cytology , ADP-ribosyl Cyclase 1/metabolism , Antigens, CD34/metabolism , Cell Differentiation/genetics , Cell Differentiation/physiology , Coculture Techniques/methods , Fetal Blood/cytology , Humans
2.
Cerebellum Ataxias ; 2: 12, 2015.
Article in English | MEDLINE | ID: mdl-26445675

ABSTRACT

BACKGROUND: Many studies are in the literature on the ANP and oxytocin-presence in the brain, but very few studies with controversial results are reported on the presence of these peptides in the cerebellum. This immunohistochemical study investigates on the ANP and oxytocin-presence in the cerebellum of the adult rat and mouse rodents. RESULTS: This study, firstly, evidences the ANP- immunopositivity in cerebellar cortex of both rat and mouse rodents. In rat the molecular layer presents some few immunopositive fibers, but no neuron resulted immunopositive; the granular and Purkinje cells are immunopositive. In mouse the cerebellar cortex ANP-immunopositivity is present in all layers. The oxytocin-presence in the rat the afferent fibers are immunopositive are in the granular layer; in mouse the OT-immunopositivity is in the molecular layer only. CONCLUSIONS: This study, firstly, shows that ANP and OT are present in the cerebellar cortex both in rat and mouse rodents. In the mouse cerebellar cortex ANP-presence is more diffuse and OT- localization differences in the two species.

3.
Anticancer Res ; 34(8): 4153-9, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25075042

ABSTRACT

BACKGROUND: Heat shock proteins (Hsps) assist other proteins in their folding and drive the degradation of defective proteins. During evolution, these proteins have also acquired other roles. Hsp10 is involved in immunomodulation and tumor progression. Hsp90 stabilizes a range of "client" proteins involved in cell signaling. The present study evaluated the expression levels of Hsp10 and Hsp90 in normal mucosa and adenocarcinoma samples of human large bowel. MATERIALS AND METHODS: Samples of normal mucosa and adenocarcinoma were collected and Reverse transcriptase-polymerase chain reaction RT-PCR, western blotting (WB) analyses, as well as immunohistochemistry were performed to evaluate the expression levels of Hsp10 and Hsp90. RESULTS: RT-PCR showed a higher gene expression of Hsp10 and Hsp90 in adenocarcinoma samples compared to healthy mucosa. WB results confirmed these findings. Immunohistochemistry revealed higher levels of Hsp10 in adenocarcinoma in both the epithelium and the lamina propria, while Hsp90 expression was higher in the adenocarcinoma samples only in the lamina propria. CONCLUSION: Hsp10 and Hsp90 may be involved in large bowel carcinogenesis.


Subject(s)
Adenocarcinoma/chemistry , Chaperonin 10/physiology , Colonic Neoplasms/chemistry , HSP90 Heat-Shock Proteins/physiology , Intestinal Mucosa/chemistry , Adenocarcinoma/etiology , Blotting, Western , Chaperonin 10/analysis , Chaperonin 10/genetics , Colonic Neoplasms/etiology , HSP90 Heat-Shock Proteins/analysis , HSP90 Heat-Shock Proteins/genetics , Humans , Immunohistochemistry , Reverse Transcriptase Polymerase Chain Reaction
4.
Folia Histochem Cytobiol ; 51(1): 55-8, 2013.
Article in English | MEDLINE | ID: mdl-23690218

ABSTRACT

Our immunohistochemical study shows that atrial natriuretic peptide (ANP) is present in both human fetal and adult parotid gland. In the fetuses ANP is localized in cell clusters, while in adult parotid gland, the ANP is seen only in the wall of intra- and extralobular ducts. The results suggest that ANP might play a role in the differentiation of the parotid gland similarly as in brain and that during fetal growth ANP may play a role in the regulating the secretion of primitive salivary fluid, even if acini are still not developed.


Subject(s)
Atrial Natriuretic Factor/metabolism , Fetus/embryology , Fetus/metabolism , Gestational Age , Parotid Gland/metabolism , Adult , Fetus/cytology , Humans , Male , Parotid Gland/cytology
5.
Curr Stem Cell Res Ther ; 8(1): 39-45, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23278911

ABSTRACT

Cardiomyopathies are still the first cause of death in the world. The identification of resident stem cells, comprising those derived from sub-endocardial stroma, suggests the possible self regeneration of the heart under autocrine/paracrine modulation in the cardiac microenvironment. Nevertheless, because of the limited in vivo regeneration potential of damaged cardiac tissue, the use of drugs and ultimately cardiac transplantation remain the common treatments of heart diseases and defects. The differentiative potential of embryonic and mesenchymal stem cells (MSCs) derived from different tissues (such as bone marrow and adipose tissue) was extensively explored in cell therapy for regenerative medicine. Many groups have been focused, in recent years, on isolation, characterization, and differentiation potential of MSCs derived from perinatal (or extraembryonic) tissues, mainly the placenta and the human umbilical cord. In this review, we summarized recent works about the stemness of Wharton's jelly stromal cells and their potential in cardiac regeneration with favourable use in cell therapy and regenerative medicine. The peculiar features of these cells, as the expression of cardiac-specific transcription factors and immunomodulatory molecules suggest that human umbilical cord may be considered as a reliable alternative source of MSC useful for advanced therapy in cardiac regenerative medicine.


Subject(s)
Cardiology , Cardiovascular Diseases/therapy , Mesenchymal Stem Cells/cytology , Regenerative Medicine , Wharton Jelly/cytology , Humans
6.
Odontology ; 101(2): 233-8, 2013 Jul.
Article in English | MEDLINE | ID: mdl-22349931

ABSTRACT

BACKGROUND: Odontogenic myxoma (OM) is a benign, locally invasive, non-metastasizing neoplasm of the jaw bones. Despite the benign nature of these lesions, there is a high rate of recurrence and the current recommended therapy, depending on the size and behaviour of the lesion, can vary from curettage with peripheral ostectomy, segmental resection up to radical resections for more aggressive lesions. OM is a rare tumour which occurs predominantly in the third decade of life and it is rare in children. Matrix metalloproteinases (MMPs) are a family of extracellular endopeptidases responsible for the degradation and remodelling of extracellular matrix, they are known to be involved in the progression and invasiveness of many types of tumour. MMPs have been studied in OM because of their well-known role in extracellular matrix degradation, tumour invasion and recurrence. CLINICAL CASE REPORT: We report a case of OM in a 6-year-old boy. A conservative excision was accomplished. The mass was excised without affecting the mandibular bone and the inferior alveolar nerve. Curettage and removal of the first right inferior molar were performed. After 6-month follow-up, no evidence of recurrence was found. EXPERIMENTAL DATA: We investigated the expression of MMP-2 and MMP-9 in this case of OM in a child. RT-PCR showed the expression of both MMP-2 and MMP-9 mRNAs. Immunohistochemistry showed a weak MMP-2 protein expression while MMP-9 protein was not detected. CONCLUSION: In this case of OM in a child, we report lack of recurrence after excision associated with low MMP-2 protein expression and absence of MMP-9. We believe it is worthy to deeply investigate the relationship between MMPs expression and OM behaviour with the aim to use MMPs as prognostic and/or therapeutic markers in OM.


Subject(s)
Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Myxoma/enzymology , Odontogenic Tumors/enzymology , Base Sequence , Child , DNA Primers , Humans , Male , Myxoma/pathology , Odontogenic Tumors/pathology , Reverse Transcriptase Polymerase Chain Reaction
7.
Folia Histochem Cytobiol ; 50(4): 497-503, 2012.
Article in English | MEDLINE | ID: mdl-23264211

ABSTRACT

The aim of the study was to assess the involvement of apoptotic factors, cytokeratins and metalloproteinase-9 in the histogenesis of both Epithelialized Gingival Lesions (EGL) and Periapical Lesions (PAL). 55 consecutive patients, 30 with PAL and 25 with EGL, were selected for the study after clinical and radiological examinations. The PAL patients had severe periapical lesions and tooth decay with exposure of the pulp chamber.All PAL and EGL biopsies were surgically extracted, fixed in 10% buffered formalin, and processed for routine light microscopy. Ten biopsies of each category were processed for immunohistochemistry (IHC). Serial paraffin sections were stained by IHC with appropriate antibodies to detect cytokeratins (CKs) 1, 5, 8, 10 and 14, caspase-3 and -9, metalloproteinase-9, and for PCNA and TUNEL assays. Both PAL and EGL showed a high expression of the cytokeratin 1, 5 and 8 with higher expression in EGL. Moreover, CK10 was markedly less intense expressed in EGL compared to PAL, while CK14 was almost three times stronger expressed in EGL. The expression of caspase-3 and -9 was stronger in PAL compared to EGL, however, the difference was only significant for caspase-9. In PAL apoptosis detected by TUNNEL method and the expression of MMP-9 were higher than in EGL, whereas PCNA was significantly more expressed in EGL. The results clearly suggest that both lesions have exclusively an epithelial origin and that epithelial proliferation was correlated with the degree of apoptosis in both entities. PAL and EGL presented mostly similar cytokeratin expression except for CK10 and CK14, though with marked differences in the distribution and intensity of IHC reactions. Finally, the degradation of extracellular matrix in both lesions could be partially attributed to the strong presence of MMP-9.


Subject(s)
Apoptosis Regulatory Proteins/metabolism , Epithelium/enzymology , Gingiva/pathology , Keratins/metabolism , Matrix Metalloproteinase 9/metabolism , Periapical Granuloma/enzymology , Periapical Granuloma/pathology , Apoptosis , Caspase 3/metabolism , Caspase 9/metabolism , Epithelium/pathology , Humans , Immunohistochemistry , Proliferating Cell Nuclear Antigen/metabolism
8.
Folia Histochem Cytobiol ; 49(2): 211-8, 2011.
Article in English | MEDLINE | ID: mdl-21744319

ABSTRACT

Full-term human umbilical cord contains three blood vessels: two arteries coiled around a vein and surrounded by Wharton's jelly, a mucous tissue with few mesenchymal stromal cells and abundant extracellular matrix. Umbilical vessels lack innervations, thus endothelial cells must play a role in the control of blood flow. The aim of this study was to investigate in human umbilical cord the expression of five peptides that could be involved in the regulation of vascular tone: Orphanin FQ, Oxytocin, Atrial Natriuretic Peptide (ANP), endothelial Nitric Oxide Synthase (eNOS) and inducible Nitric Oxide Synthase (iNOS). The expression of these molecules in full-term human umbilical cord was investigated through immunohistochemistry and RT-PCR. Immunoreactivity for Orphanin FQ was detected in Wharton's jelly, vessel musculature and endothelium; Oxytocin, ANP and eNOS were expressed by the umbilical epithelium, Wharton's jelly and endothelium, whereas iNOS only by endothelial cells. RT-PCR analysis showed transcriptional expression of Oxytocin, ANP and eNOS mRNAs. The presence of Orphanin, Oxytocin, ANP, eNOS and iNOS proteins was identified in the human umbilical cord. mRNA expression for Oxytocin, ANP and eNOS suggest that these molecules are synthesized by umbilical cord cells themselves. The expression of these vasoactive molecules could be part of a general mechanism locally regulating vascular tone.


Subject(s)
Atrial Natriuretic Factor/metabolism , Blood Vessels/metabolism , Nitric Oxide Synthase Type III/metabolism , Nitric Oxide Synthase Type II/metabolism , Opioid Peptides/metabolism , Oxytocin/metabolism , Umbilical Cord/metabolism , Animals , Atrial Natriuretic Factor/genetics , Female , Gene Expression Regulation , Humans , Immunohistochemistry , Male , Nitric Oxide Synthase Type II/genetics , Nitric Oxide Synthase Type III/genetics , Opioid Peptides/genetics , Oxytocin/genetics , Rats , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , Umbilical Cord/cytology , Nociceptin
9.
J Mol Histol ; 41(6): 367-77, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20936527

ABSTRACT

Matrix metalloproteinases (MMPs) are extracellular zinc-dependent endopeptidases involved in the degradation and remodelling of extracellular matrix in physiological and pathological processes. MMPs also have a role on cell proliferation, migration, differentiation, angiogenesis and apoptosis. Umbilical cord is a special organ subjected to many changes during pre-natal life and whose cells can maintain a certain degree of plasticity also in post-natal period; for example recently they have been used as a source of stem cells. In this work we investigated the expression of MMPs in human umbilical cord and human umbilical vein endothelial cells (HUVEC) though immunohistochemistry, RT-PCR and gelatin zymography. MMP-2 protein is expressed in the amniotic epithelium of human umbilical cord and in few sub-epithelial fibroblasts, while MMP-3 and MMP-10 only in the umbilical epithelium. MMP-8, MMP-9 and MMP-13 immunoreactivity is localised in the epithelium and in Wharton's jelly mesenchymal cells. Immunocytochemistry also revealed protein expression for MMP-2, 3, 8, 9 and 10 in cultured HUVEC. In agreement with immunohistochemical data, RT-PCR analysis performed on samples of whole umbilical cord confirmed the transcriptional expression for the genes encoding all the six matrix metalloproteinases investigated, while in HUVEC only the expression of MMP-2, 3, 9, 10 and 13 mRNAs was detected. Gelatin zymography showed a clear MMP-2 and MMP-9 enzymatic activity in the conditioned medium of HUVEC at different culture passages, suggesting that HUVEC secrete gelatinases, that afterwards undergo extracellular activation, and this ability is not affected by passage number.


Subject(s)
Endothelial Cells/enzymology , Matrix Metalloproteinases/metabolism , Umbilical Cord/enzymology , Umbilical Veins/cytology , Cells, Cultured , Endothelial Cells/cytology , Gene Expression Regulation, Enzymologic , Humans , Immunohistochemistry , Matrix Metalloproteinase 10/metabolism , Matrix Metalloproteinase 13/metabolism , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 3/metabolism , Matrix Metalloproteinase 8/metabolism , Matrix Metalloproteinase 9/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Umbilical Veins/enzymology
10.
Clin Anat ; 23(7): 743-9, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20803570

ABSTRACT

Giovanni Filippo Ingrassia was born five centuries ago in Regalbuto, a small town in the center of Sicily. After his medical course in Padua, under the guidance of Vesalius and Fallopius, he gained international fame as a physician and was recruited as a Professor of human anatomy in Naples and later in Palermo. He is remembered as "the new Galen" or "the Sicilian Hippocrates." He contributed to the knowledge of human anatomy through the description of single bones rather than the whole skeleton. In particular, he was the first to describe the "stapes," the "lesser wings of the sphenoid" and various other structures in the head (probably the pharyngotympanic tube) as well as in the reproductive system (corpora cavernosa and seminal vesicles). He was also a pioneer in the study of forensic medicine, hygiene, surgical pathology, and teratology. As Protomedicus of Sicily, he developed the scientific culture in this country. During those years, he faced the spread of malaria and plague with competence and authoritativeness. Indeed, he was one of the first physicians to suppose that certain diseases could be transmitted between individuals, therefore, introducing revolutionary measures of prevention. He is remembered for his intellectual authority and honesty. Five-hundred years after his birth, his teaching is still alive. In this article, we survey the life and contribution of this pioneer of early anatomical study.


Subject(s)
Osteology/history , Bone and Bones/anatomy & histology , Ear Ossicles/anatomy & histology , History, 16th Century , Humans , Male , Penis/blood supply , Sicily
11.
Folia Histochem Cytobiol ; 48(1): 68-70, 2010 Jan 01.
Article in English | MEDLINE | ID: mdl-20529818

ABSTRACT

Atrial natriuretic peptide was found in the heart of vertebrates, we studied the ANP presence in the heart of Ciona intestinalis. This is animal is very important because of the its evolutionary position between invertebrates and vertebrates. ANP presence was only revealed in myoepithelial cells of the myocardium. Results suggest the hypothesis that ANP is present not only in the vertebrates but also in the invertebrates and in Ciona heart ANP might play a similar role like in the heart of vertebrates.


Subject(s)
Atrial Natriuretic Factor/metabolism , Ciona intestinalis/metabolism , Myocardium/metabolism , Animals , Ciona intestinalis/cytology , Myocardium/cytology
12.
Folia Histochem Cytobiol ; 48(4): 555-63, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21478098

ABSTRACT

Cyclooxigenase (COX) is the rate-limiting enzyme for the conversion of arachidonic acid (AA) to prostaglandins (PGs). Two isoforms of COX have been identified: COX-1 is constitutively expressed in many cells and is involved in cell homeostasis, angiogenesis and cell-cell signalling; COX-2 is not expressed in normal condition however it is strongly expressed in inflammation. The oral cavity is constantly exposed to physical and chemical trauma that could lead to mucosal reactions such as hyperplasia, dysplasia and cancer. Early diagnosis is the most important issue to address for a positive outcome of oral cancer; therefore it would be useful to identify molecular markers whose expression is associated with the various stages of oral cancer progression. Since COX enzyme has been involved, with different mechanisms, in the development and progression of malignancies we decided to investigate the expression and localization of COX-1 and COX-2 in normal human oral mucosa and three different pathologies (hyperplasia, dysplasia and carcinoma) by immunohistochemistry and RT-PCR. COX-1 mRNA and protein have been detected already in normal oral mucosa and their expression progressively increases from normal samples towards hyperplasia, dysplasia and finally carcinoma. On the contrary, COX-2 is not expressed in the normal tissue, starts to be expressed in hyperplasia, reaches the maximum activation in dysplasia and then starts to be downregulated in carcinoma.


Subject(s)
Cyclooxygenase 1/metabolism , Cyclooxygenase 2/metabolism , Mouth Mucosa/enzymology , Mouth Mucosa/pathology , Mouth Neoplasms/enzymology , Precancerous Conditions/enzymology , Cyclooxygenase 1/genetics , Cyclooxygenase 2/genetics , Gene Expression Regulation, Neoplastic , Humans , Hyperplasia , Immunohistochemistry , Mouth Neoplasms/pathology , Neoplasm Staging , Precancerous Conditions/pathology , Reverse Transcriptase Polymerase Chain Reaction
13.
Angle Orthod ; 79(6): 1119-25, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19852603

ABSTRACT

OBJECTIVE: To test the hypothesis that some metalloproteinases (MMP-2, MMP-9) and inducible nitric oxide synthetase (iNOS) enzymes in dental pulp samples do not vary when subjected to orthodontic treatment. MATERIALS AND METHODS: Human dental pulps were taken from male and female patients (N=10; age 10-14 years). A straight wire technique was used with nickel-titanium or steel archwires. The increase of pressure applied on teeth was gradual. Five patients were subjected to premolar extractions after 14 months of treatment and one after 24 months. Samples were Bouin-fixed, paraffin-embedded, and afterwards processed for immunohistochemistry using anti-MMP-2, anti-MMP-9, and anti-iNOS antibodies. RESULTS: A reduction of MMP-2, MMP-9, and iNOS expression occurred in treated samples. This became more evident with increased treatment time. CONCLUSION: The hypothesis is rejected. The reduction of expression of those proteins revealed a time-dependent relationship.


Subject(s)
Dental Pulp/enzymology , Matrix Metalloproteinase 2/analysis , Matrix Metalloproteinase 9/analysis , Nitric Oxide Synthase Type II/analysis , Tooth Movement Techniques , Adolescent , Bicuspid/enzymology , Biomechanical Phenomena , Child , Dental Alloys , Dental Pulp/pathology , Female , Follow-Up Studies , Humans , Male , Malocclusion, Angle Class II/therapy , Nickel , Odontoblasts/enzymology , Orthodontic Wires , Pressure , Steel , Stress, Mechanical , Time Factors , Titanium
14.
J Cell Physiol ; 221(1): 189-94, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19492417

ABSTRACT

Both leptin and vascular endothelial growth factor (VEGF) are growth and angiogenic cytokines that are upregulated in different types of cancer and have been implicated in neoplastic progression. Here we investigated the molecular mechanism by which leptin and VEGF expression are regulated in colon cancer by epidermal growth factor (EGF). In colon cancer cell line HT-29, EGF induced the binding of signal transducer and activator transcription 3 (STAT3) to STAT3 consensus motifs within the VEGF and leptin promoters and stimulated leptin and VEGF mRNA and protein synthesis. All these EGF effects were significantly blocked when HT-29 cells were treated with an inhibitor of the phosphoinositide 3-kinase (PI3K) pathway, LY294002, or with small interfering RNA (siRNA) targeting STAT3. Thus, our study identified the EGF/PI3K/STAT3 signaling as an essential pathway regulating VEGF and leptin expression in EGF-responsive colon cancer cells. This suggests that STAT3 pathways might constitute attractive pharmaceutical targets in colon cancer patients where anti-EGF receptor drugs are ineffective.


Subject(s)
Colorectal Neoplasms/enzymology , Epidermal Growth Factor/metabolism , Leptin/metabolism , Neovascularization, Physiologic , Phosphatidylinositol 3-Kinases/metabolism , STAT3 Transcription Factor/metabolism , Vascular Endothelial Growth Factor A/metabolism , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Colorectal Neoplasms/genetics , Gene Expression Regulation, Neoplastic/drug effects , Gene Silencing/drug effects , HT29 Cells , Humans , Leptin/genetics , Neovascularization, Physiologic/drug effects , Promoter Regions, Genetic/genetics , Protein Binding/drug effects , RNA, Messenger/genetics , RNA, Messenger/metabolism , Up-Regulation/drug effects , Vascular Endothelial Growth Factor A/genetics
15.
Med Secoli ; 19(2): 481-93, 2007.
Article in Italian | MEDLINE | ID: mdl-18450029

ABSTRACT

Born on 7th April 1668 in Modica, Ciceronian 'Agrum Motucanum', the Modican county of Chiaramontes and Chiabreras, Tommaso Campailla, a poet and a physician, is mostly known as the author of a philosophical poem in octaves--Adam or the Created World. In his 1727 Problemi naturali [Natural Problems], his essay Del disordinato discorso dell'uomo [On Man's Disorderly Discourse] distinguishes itself by its intellectual wit on both the speculative and the experimental research aspects. He formulates concepts on the darkness which often reason has to fare through; he substantializes the body/soul syncretic dimension, and underlines how this disrupts the perfect bodily mechanism. His observations are born in a scientific and historical period which was absorbed within an iatromechanical scenario of which they are reliable proofs and physiological foundations. If on the one hand he reduces the spiritual (psychical) stance to a physical one, on the other hand he gives substance to his questioning his own inner torments, his own hypochondriac being. He died of apoplexy aged 72, on 7th February 1740.


Subject(s)
Famous Persons , Hypochondriasis/history , Literature, Modern/history , Poetry as Topic/history , History, 17th Century , History, 18th Century , Humans , Italy , Male , Physicians/history
16.
Ital J Anat Embryol ; 111(1): 23-30, 2006.
Article in English | MEDLINE | ID: mdl-16736715

ABSTRACT

In this work we used a virtual approach to study the human liver by three-dimensional geometrical models. We built the models through computer aided geometric modelling techniques starting from pictures taken during both real dissections and diagnostic medical imaging. The results show in a complete modular synthesis and with a schematic iconology the structural organization of this organ in a logic sequence of layers and topographic and spatial relationship among its components. This approach represents an amazing support to clinical anatomy for teaching and research.


Subject(s)
Computer Simulation , Liver/anatomy & histology , Models, Anatomic , Databases, Factual , Hepatic Artery/anatomy & histology , Humans , Libraries, Digital , Portal Vein/anatomy & histology
17.
J Cell Physiol ; 207(3): 654-9, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16447252

ABSTRACT

The putative role of TP53 and p16(INK4A) tumor suppressor genes and Ras oncogenes in the development and progression of salivary gland neoplasias was studied in 28 cases of pleomorphic adenomas (PA), 4 cases of cystic adenocarcinomas, and 1 case of carcinoma ex-PA. Genetic and epigenetic alterations in the above genes were analyzed by Polymerase Chain Reaction/Single Strand Conformational Polymorphism (PCR/SSCP) and sequencing and by Methylation Specific-PCR (MS-PCR). Mutations in TP53 were found in 14% (4/28) of PAs and in 60% (3/5) of carcinomas. Mutations in H-Ras and K-Ras were identified in 4% (1/28) and 7% (2/28) of PAs, respectively. Only 20% (1/5) of carcinomas screened displayed mutations in K-Ras. p16(INK4A) promoter hypermethylation was found in 14% (4/28) of PAs and 100% (5/5) carcinomas. All genetic and epigenetic alterations were detected exclusively in the epithelial and transitional tumor components, and were absent in the mesenchymal parts. Our analysis suggests that TP53 mutations and p16(INK4A) promoter methylation, but not alterations in the H-Ras and K-Ras genes, might be involved in the malignant progression of PA into carcinoma.


Subject(s)
Adenoma/genetics , Adenoma/pathology , Cell Transformation, Neoplastic/genetics , Cell Transformation, Neoplastic/pathology , Cyclin-Dependent Kinase Inhibitor p16/genetics , Tumor Suppressor Protein p53/genetics , Adenoma/metabolism , Base Sequence , Cell Transformation, Neoplastic/metabolism , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Disease Progression , Epigenesis, Genetic/genetics , Genotype , Humans , Methylation , Mutation/genetics , Proto-Oncogene Proteins p21(ras)/genetics
18.
Ital J Anat Embryol ; 109(3): 155-66, 2004.
Article in English | MEDLINE | ID: mdl-15597916

ABSTRACT

On 11 March 2004, the Section of Human Anatomy of Palermo was dedicated and registered to the anatomist Emerico Luna (Palermo 1882-1963) with a ceremony (moderated by Giovanni Zummo) with the participation of institutional personalities and Italian anatomists. Luna, who was an acute morphologist and a scholar of Riccardo Versari (1865-1943), was the continuator of Francesco Todaro's Anatomical School and occupied the Chair at the University of Palermo that had belonged to Levi since 1919. His wide histo-anatomical culture culminates in the collaboration to the "Trattato di Neurologia", the richly composed treatise by Bertelli (1931). Then his studies and his teaching reached to the Anatomia Clinica Regionale (1951). In charge of Histology and Normal Human Anatomy in 1920-21, he became a full professor and a master till 1952. He had so many students: among them Ignazio Fàzzari (1889-1986) who had the chair in the University of Florence, Alberto Monroy who had the charge of Compared Anatomy in the University of Palermo and Arcangelo Pasqualino from Marineo. Luna was co-founder and leader of the "Italian Society of Anatomy". He developed an intense research above all on the nervous system, the connective tissues, the arteries of the brain, and the experimental embryology, developing the radiological and clinical anatomy. He also dedicated himself to literature writing in 1953, among the scientific and literary works, a booklet titled Alla Fiera Delle Fantasie where he discuss the fantasy in a style that recall the literary evasion of the last period of crepuscolarism.


Subject(s)
Anatomy/history , Anatomy/education , Animals , History, 20th Century , Humans , Italy
19.
Ital J Anat Embryol ; 108(4): 223-30, 2003.
Article in English | MEDLINE | ID: mdl-14974505

ABSTRACT

In this work we studied the inguinal-abdominal region and the inguinal canal using three-dimensional geometrical models. We built the models through computer aided geometric modeling techniques on the basis of observations during real dissections, operations and diagnostic medical imaging. The obtained models show in a complete modular synthesis and with a schematic iconology the structural organization of the anatomical districts in a logic sequence of layers and topographic and spatial relationships among its components. The models represent an amazing support to anatomy and clinical anatomy for teaching and research purposes on organogenesis, surgery and diagnosis.


Subject(s)
Image Processing, Computer-Assisted/methods , Inguinal Canal/anatomy & histology , Models, Anatomic , Abdominal Muscles/anatomy & histology , Abdominal Muscles/diagnostic imaging , Abdominal Muscles/physiology , Anatomy/education , Anatomy/methods , Hernia, Inguinal/pathology , Hernia, Inguinal/physiopathology , Humans , Inguinal Canal/diagnostic imaging , Inguinal Canal/physiology , Ligaments/anatomy & histology , Ligaments/diagnostic imaging , Ligaments/physiology , Magnetic Resonance Imaging , Male , Software , Spermatic Cord/anatomy & histology , Spermatic Cord/diagnostic imaging , Spermatic Cord/physiology , Testis/embryology , Tomography, X-Ray Computed
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