Abstract-Cardiomyocyte regeneration is limited in adult life. Thus, the identification of a putative source of cardiomyocyte progenitors is of great interest to provide a usable model in vitro and new perspective in regenerative therapy. Key Words: cardiomyocytes Ⅲ adipose tissue Ⅲ differentiation Ⅲ stem cells Ⅲ cell therapy C ardiomyocyte differentiation mainly takes place during neonatal and perinatal life. In adult life, the regenerative potential of cardiac tissue is limited and is not sufficient to prevent from the degeneration occurring in pathological conditions such as myocardial infarction. 1 Cell transplantation seems to be an alternative to overcome this problem. 2 This led to numerous investigations to identify a putative source of transplanted cells and to better understand cardiomyocyte proliferation and differentiation in order to drive the fate of stem cells toward this process. Different sources, ie, embryonic, fetal, and adult cells have been investigated and tested. 3-8 Among them, mesenchymal stem cells (MSCs) isolated from bone marrow are accepted to give rise to connective tissue cell types. Their differentiation toward cardiomyocyte was obtained in vitro and in vivo. However, immortalized MSCs and treatment with the DNA demethylation agent 5-azacytidine was necessary to reveal their cardiogenic potential in vitro. 6 Adipose tissues are mesodermic tissues, which develop during perinatal and postnatal life. 9 They are strongly involved in various metabolic disorders such as obesity. Tremendous changes in adipose mass are achieved through highly controlled processes such as angiogenesis, precursor recruitment, proliferation, differentiation, dedifferentiation, and apoptosis as well. More recently, differentiation of cells derived or purified from adipose tissue toward phenotypes different from adipocyte was described. 10 -13 However, the characterization of cells with such potential remains to be done. The present statement is that adipose tissue consists of mature adipocytes and the stroma vascular fraction (SVF). SVF is a heterogeneous cell population. Among them the identified ones are vascular cells (endothelial, smooth muscle cell, circulating blood cells) and an undefined fibroblast-like cell population recently described as a multipotential stem cell population for various mesodermic lineage. 10 -13 This led us to test the in vitro cardiomyogenic potential of cells purified from adipose tissue. In the results reported in this study, adipose-derived cells (SVF cells) from primary culture spontaneously differentiate into cells with morphological, molecular, and functional properties of cardiomyocytes. Materials and Methods AnimalsSix-week-old adult male C57Bl/6N mice (Harlan, France) were housed in conventional animal quarters (SPS barrier facility). Mice were killed by cervical dislocation under CO 2 anesthesia. All procedures were performed according to SELASA norms.

In patients with old myocardial infarction, treatment with skeletal myoblast in conjunction with coronary artery bypass is safe and feasible and is associated with an increased global and regional left ventricular function,improvement in the viability of cardiac tissue in the infarct area and no induction of arrhythmias.

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The biofilm-forming capacity of 972 clinical isolates of Staphylococcus aureus was tested using a high-throughput polystyrene 96-peg plate format. Isolates of S. aureus were collected from patients in hospitals throughout Scotland from 2004 to 2006; 763 of these were meticillinresistant S. aureus (MRSA) and 209 were meticillin-sensitive S. aureus (MSSA). The biomass of each biofilm was quantified using a crystal violet staining technique. Isolates were divided into those that formed fully established biofilms, moderately attached biofilms and weakly adherent biofilms by comparison with a known biofilm-forming strain. The majority of MRSA (53.8 %) and MSSA (43.5 %) isolates formed moderately attached biofilms. Fully established biofilms were formed by 20.5 % of MRSA isolates and 28.0 % of MSSA isolates, whilst 25.7 % of MRSA isolates and 28.5 % of MSSA isolates formed negligible biofilms. There was no significant correlation between susceptibility to meticillin and biofilm formation (P50.77). MRSA isolates were divided into clonal types (EMRSA-15, EMRSA-16 and sporadic isolates) based on PFGE genotyping results. EMRSA-15 isolates formed significantly more moderately and fully established biofilms than EMRSA-16 isolates (P,0.001). S. aureus strains isolated from the skin of patients had a significantly greater capacity to form biofilms than isolates from other body sites, including the blood. Microscopic examination of biofilms by scanning electron microscopy (SEM) revealed that poorly adherent biofilm formers failed to colonize the entire surface of the peg, whilst moderately adherent biofilm formers grew in uniform monolayers but failed to develop a mature three-dimensional structure. SEM analysis of an isolate representative of the group that formed fully established biofilms confirmed that this isolate developed a dense biofilm with a textured, multi-layered, three-dimensional structure.

Several features and functions of a Candida albicans gene, PGA10 (also designated as RBT51), coding for a putative polypeptide species belonging to a subset of fungal proteins containing an eight-cysteine domain referred as CFEM (Common in several Fungal Extracellular Membrane proteins), are described. The ORF of the gene (ORF19.5674) encoded a protein of 250 amino acids, with a predicted molecular mass of 25.17 kDa. The product of the PGA10 gene also exhibited some features reminiscent of a class II-type hydrophobin. Deletion of PGA10 resulted in a cascade of pleiotropic effects, mostly affecting cell-surface-related properties. Thus, the null pga10Delta mutant displayed an increased sensitivity to cell-wall-perturbing agents and formed fragile biofilms that appeared partially split and weakly attached to the substratum. The biofilm-forming ability of several C. albicans mutants with single, double and triple deletions of genes encoding other protein species also containing the CFEM domain (RBT5 and WAP1/CSA1) was determined. These mutants also exhibited an abnormal ability to form biofilms. Overall, the evidence presented here suggests that fungal proteins containing the CFEM domain (Pga10p/Rbt51p, Rbt5p and Wap1p/Csa1p) may play a key role in the formation, development and/or maintenance of the biofilm structure in C. albicans.

In patients with previous myocardial infarction, treatment with skeletal myoblasts in conjunction with coronary artery bypass is safe and feasible and is associated with an increased global and regional left ventricular function, improvement in viability, and perfusion of cardiac tissue and no significant incidence of arrhythmias.

Several biological features of Candida albicans genes (PGA10, RBT5 and CSA1) coding for putative polypeptide species belonging to a subset of fungal proteins containing an eight-cysteine domain referred as common in several fungal extracellular membrane (CFEM) are described. The deletion of these genes resulted in a cascade of pleiotropic effects. Thus, mutant strains exhibited higher cell surface hydrophobicity levels and an increased ability to bind to inert or biological substrates. Confocal scanning laser microscopy using concanavalin A-Alexafluor 488 (which binds to mannose and glucose residues) and FUN-1 (a cytoplasmic fluorescent probe for cell viability) dyes showed that mutant strains formed thinner and more fragile biofilms. These apparently contained lower quantities of extracellular matrix material and less metabolically active cells than their parental strain counterpart, although the relative percentage of mycelial forms was similar in all cases. The cell surface of C. albicans strains harbouring deletions for genes coding CFEM-domain proteins appeared to be severely altered according to atomic force microscopy observations. Assessment of the relative gene expression within individual C. albicans cells revealed that CFEM-coding genes were upregulated in mycelium, although these genes were shown not to affect virulence in animal models. Overall, this study has demonstrated that CFEM domain protein-encoding genes are pleiotropic, influencing cell surface characteristics and biofilm formation.

This investigation was carried out to show the possible association between groups of children with extreme values of copper and zinc concentrations and cardiovascular risk indicators. Serum copper and zinc concentrations were analysed in a group of 3887 children from Navarra, Spain (both sexes. aged 4-17 years). Hypertension, unfavourable serum lipid profile (total cholesterol, high density lipoprotein cholesterol, low density lipoprotein cholesterol, triglycerides, and cholesterol/HDL and LDL/HDL ratios), and degree of adiposity (weight, height, subcutaneous skinfolds, Quetelet's index and mean of subcutaneous skinfolds) were evaluated. Positive correlation was found between several lipid parameters and copper and zinc concentrations, i.e. degree of correlation related with age, except for copper/HDL and triglycerides/zinc ratios, where correlation remained negative at all points. Copper levels were correlated with adiposity parameters in an age-dependent fashion (Quetelet's index: r = 0.01 for ages 4-7 years to r = 0.10, p < 0.01 for ages 14-17 years; mean skinfold thickness: r = 0.05 for ages 4-7 years up to r = 0.18, p < 0.01 for ages 14-17 years). Most correlations between lipid parameters and copper and zinc are markedly amplified if adiposity parameters are taken into account. However, the only significant association was the established relation between high copper concentrations (> x + 2SD) and unfavourable serum lipid profile (LDL/HDL > 2.2).