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1.
Cell Calcium ; 43(5): 457-68, 2008 May.
Article in English | MEDLINE | ID: mdl-17825906

ABSTRACT

Reactive oxygen species (ROS) have long been considered as toxic by-products of aerobic metabolism and appear involved in the pathogenesis of degenerative diseases. The physiological role of ROS as second messengers in cell signal transduction is, on the other hand, increasingly recognized. Here we investigated the effects of H(2)O(2) and extracellular nucleotides on calcium signalling in four osteoblastic cell lines. In the highly differentiated HOBIT cells, sensitive to nanomolar concentrations of ADP and UTP, millimolar H(2)O(2) induced oscillatory increases of the cytosolic calcium concentration followed by a steady and sustained calcium increase. Long lasting rhythmic calcium activity was induced by micromolar H(2)O(2) doses. The H(2)O(2)-induced calcium signals, due to both release from intracellular stores and influx from the extracellular milieu, were totally prevented by incubating the cells with the P2 receptor antagonist suramin or with the ATP/ADP hydrolyzing enzyme apyrase. In the osteosarcoma SaOS-2 cells micromolar H(2)O(2) failed to evoke calcium signals and millimolar H(2)O(2) induced a slowly developing calcium influx which was unaffected by suramin and apyrase. These cells responded to micromolar concentrations of ATP and ADP, but were largely insensitive to UTP. ROS 17/2.8 osteosarcoma cells were totally insensitive to ATP, ADP and UTP in keeping with the evidence that these cells lack functional purinergic receptors. In these cells, H(2)O(2) up to 1mM did not increase the cytosolic calcium concentration. In ROS/P2Y(2) cells, stably expressing the P2Y(2) receptor, spontaneous calcium oscillations were observed in 38% of the population and nanomolar concentration of extracellular ATP or UTP activated oscillations in quiescent cells. Spontaneous calcium signals were inhibited by suramin and apyrase. In these cells H(2)O(2) induced oscillatory calcium activity that was blocked by suramin and apyrase. The sensitivity of ROS/P2Y(2) cells to UTP decreased significantly in the presence of DTT, which was effective also in inhibiting spontaneous calcium oscillations. On the other hand, the membrane-impermeant thiol oxidant DTNB induced calcium oscillations that were inhibited by incubating the cells with suramin or apyrase. Since peroxide did not increase extracellular ATP in these cell lines, we propose that, in osteoblasts, mild oxidative conditions could activate purinergic signalling through the sensitization of P2Y(2) receptor.


Subject(s)
Adenine Nucleotides/pharmacology , Calcium Signaling , Hydrogen Peroxide/pharmacology , Osteoblasts/metabolism , Receptors, Purinergic P2/metabolism , Adenosine Diphosphate/pharmacology , Adenosine Triphosphate/pharmacology , Cell Line , Cell Line, Tumor , Humans , Osteoblasts/drug effects , Receptors, Purinergic P2Y2 , Uridine Triphosphate/pharmacology
2.
Hum Mol Genet ; 15(17): 2569-87, 2006 Sep 01.
Article in English | MEDLINE | ID: mdl-16849369

ABSTRACT

Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major cause of genetic non-syndromic hearing loss. The role of the allelic variant M34T in causing hereditary deafness remains controversial. By combining genetic, clinical, biochemical, electrophysiological and structural modeling studies, we have re-assessed the pathogenetic role of the M34T mutation. Genetic and audiological data indicate that the majority of heterozygous carriers and all five compound heterozygotes exhibited an impaired auditory function. Functional expression in transiently transfected HeLa cells showed that, although M34T was correctly synthesized and targeted to the plasma membrane, it inefficiently formed intercellular channels that displayed an abnormal electrical behavior and retained only 11% of the unitary conductance of the wild-type protein (HCx26wt). Moreover, M34T channels failed to support the intercellular diffusion of Lucifer Yellow and the spreading of mechanically induced intercellular Ca2+ waves. When co-expressed together with HCx26wt, M34T exerted dominant-negative effects on cell-cell coupling. Our findings are consistent with a structural model, predicting that the mutation leads to a constriction of the channel pore. These data support the view that M34T is a pathological variant of Cx26 associated with hearing impairment.


Subject(s)
Amino Acid Substitution , Connexins/genetics , Deafness/genetics , Genetic Predisposition to Disease , Point Mutation , Adolescent , Adult , Aged , Audiology , Calcium Signaling , Child , Child, Preschool , Coloring Agents/chemistry , Coloring Agents/pharmacokinetics , Connexin 26 , Connexins/chemistry , Connexins/metabolism , Female , Follow-Up Studies , HeLa Cells , Humans , Ion Channel Gating , Male , Middle Aged , Pedigree , Protein Structure, Tertiary , Structure-Activity Relationship , Transfection
3.
Neurobiol Dis ; 21(3): 607-17, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16442804

ABSTRACT

The X-linked form of Charcot-Marie-Tooth disease (CMTX) is caused by mutations in connexin32 (Cx32), a gap junction protein expressed by Schwann cells where it forms reflexive channels that allow the passage of ions and signaling molecules across the myelin sheath. Although most mutations result in loss of function, several studies have reported that some retain the ability to form homotypic intercellular channels. To gain insight into the molecular defect of three functional CMTX variants, S26L, Delta111-116 and R220stop, we have used several fluorescent tracers of different size and ionic charge to compare their permeation properties to those of wild-type Cx32. Although all mutations allowed the passage of the dye with the smallest molecular mass, they exhibited a clear reduction in the permeability of either one or all of the probes with respect to wild-type channels, as assessed by the percentage of injections showing dye coupling. These data reveal that a lower size cutoff distinguishes these functional CMTX variants from wild-type channels and suggest that this defect may be of pathophysiological relevance.


Subject(s)
Charcot-Marie-Tooth Disease/metabolism , Connexins/genetics , Genetic Diseases, X-Linked/metabolism , Ion Channels/metabolism , Blotting, Western , Charcot-Marie-Tooth Disease/genetics , Genetic Diseases, X-Linked/genetics , HeLa Cells , Humans , Microscopy, Fluorescence , Mutation , Patch-Clamp Techniques , Permeability , Transfection , Gap Junction beta-1 Protein
4.
Biochem Biophys Res Commun ; 339(3): 821-6, 2006 Jan 20.
Article in English | MEDLINE | ID: mdl-16325774

ABSTRACT

Bacteria belonging to the Burkholderia cepacia complex (Bcc) are interesting for their involvement in pulmonary infections in patients affected by cystic fibrosis (CF) or chronic granulomatous disease. Many Bcc strains isolated from CF patients produce high amounts of exopolysaccharides (EPS). Although different strains sometimes biosynthesise different EPS, the majority of Bcc bacteria produce only one type of polysaccharide, which is called cepacian. The polymer has a unique heptasaccharidic repeating unit, containing three side chains, and up to three O-acetyl substituents.. We here report for the first time the isolation and characterisation of a lyase active towards cepacian produced by a Bacillus sp., which was isolated in our laboratory. The enzyme molecular mass, evaluated by size-exclusion chromatography, is 32,700+/-1500Da. The enzyme catalyses a beta-elimination reaction of the disaccharide side chain beta-d-Galp-(1-->2)-alpha-d-Rhap-(1--> from the C-4 of the glucuronic acid residue present in the polymer backbone. Although active on both native and de-acetylated cepacian, the enzyme showed higher activity on the latter polymer.


Subject(s)
Burkholderia cepacia complex/metabolism , Lyases/chemistry , Lyases/metabolism , Polysaccharides, Bacterial/chemistry , Polysaccharides, Bacterial/metabolism , Binding Sites , Enzyme Activation , Lyases/isolation & purification , Molecular Weight , Polysaccharides, Bacterial/isolation & purification , Protein Binding , Substrate Specificity
5.
Biochem Biophys Res Commun ; 337(3): 799-805, 2005 Nov 25.
Article in English | MEDLINE | ID: mdl-16226720

ABSTRACT

Mutations of the GJB2 gene, encoding connexin 26, are the most common cause of hereditary congenital hearing loss in many countries and account for up to 50% of cases of autosomal-recessive non-syndromic deafness. By contrast, only a few GJB2 mutations have been reported to cause an autosomal-dominant form of non-syndromic deafness. Here, we report a family from Southern Italy affected by non-syndromic autosomal dominant post-lingual hearing loss, due to a novel missense mutation in the GJB2 gene, a threonine to asparagine amino acid substitution at codon 55 (T55N). Functional studies indicated that the mutation T55N produces a protein that, although expressed to levels similar to those of the wt counterpart, is deeply impaired in its intracellular trafficking and fails to reach the plasma membrane. The mutation T55N is located at the apex of the first extracellular loop of the protein, a region suggested to play a role in protein targeting and a site for other two mutations, G59A and D66H, causing dominant forms of deafness.


Subject(s)
Connexins/genetics , Connexins/metabolism , Genetic Testing/methods , Hearing Loss/genetics , Hearing Loss/metabolism , Risk Assessment/methods , Base Sequence , Connexin 26 , DNA Mutational Analysis/methods , Genetic Predisposition to Disease/genetics , Hearing Loss/congenital , Humans , Italy , Molecular Sequence Data , Pedigree , Polymorphism, Genetic , Risk Factors , Syndrome
6.
Biochem Biophys Res Commun ; 331(4): 1429-38, 2005 Jun 17.
Article in English | MEDLINE | ID: mdl-15883034

ABSTRACT

Extracellular nucleotides such as ATP and UTP are released in response to mechanical stimulation in different cell systems. It is becoming increasingly evident that ATP release plays a role in autocrine and paracrine stimulation of osteoblasts. Mechanical stimulation, as shear stress, membrane stretch or hypo-osmotic swelling, as well as oscillatory fluid flow, stimulates ATP release from different osteoblastic cell lines. Human osteoblast-like initial transfectant (HOBIT) cells release ATP in response to mechanical stimulation. In the present study, we show that HOBIT cells are activated by nanomolar levels of extracellular ATP, concentrations that can be detected under resting conditions and increase following hypotonic shock. Cell activation by hypotonic medium induced intracellular Ca2+ oscillations, and Egr-1 synthesis and DNA-binding activity. Quinacrine staining of living, resting cells revealed a granular fluorescence, typical of ATP-storing vesicles. Monensin prevented quinacrine staining and considerably inhibited hypotonic-induced ATP release. Finally, elevated levels of cytosolic Ca2+ activated massive ATP release and a dose-dependent loss of quinacrine granules. The contribution of a vesicular mechanism for ATP release is proposed to sustain paracrine osteoblast activation.


Subject(s)
Adenosine Triphosphate/metabolism , Osteoblasts/metabolism , Receptors, Purinergic/metabolism , Base Sequence , Cell Line , DNA Primers , Electrophoretic Mobility Shift Assay , Humans , Quinacrine/metabolism
7.
Biochem Biophys Res Commun ; 305(4): 1024-33, 2003 Jun 13.
Article in English | MEDLINE | ID: mdl-12767933

ABSTRACT

Human connexins 26 and 30 were expressed either through the bicistronic pIRES-EGFP expression vector or as EYFP-tagged chimeras. When transiently transfected in communication-incompetent HeLa cells, hCx26-pIRES transfectants were permeable to dyes up to 622 Da, but were significantly less permeable to 759 Da molecules. Under the same conditions, permeability of hCx26-EYFP fusion products was comparable to that of hCx26-pIRES, but with significant increase in diffusion at 759 Da, possibly as a consequence of having selected large fluorescent junctional plaques. Dye transfer was limited to 457 Da in hCx30-EYFP transfectants. When reconstructed from confocal serial sections, fluorescent plaques formed by hCx26-EYFP and hCx30-EYFP appeared irregular, often with long protrusions or deep invagination. Similar plaques were observed following immunostaining both in cells transfected with hCx26-pIRES and in HeLa cells stably transfected with mouse Cx26. Tissue conductance (Tg(j)) displayed significantly smaller values (28.8+/-1.8 nS) for stably transfected mCx26 than transiently transfected hCx26 (43.5+/-3.3 nS). These differences reflected in distinct functional dependence of normalized junctional conductance (G(j)) on transjunctional voltage (V(j)). The half-activation voltage for G(j) was close to +/-95 and +/-58 mV in mCx26 and hCx26, respectively. The corresponding parameters for hCx30 transfectants were Tg(j)= 45.2 +/- 3.5 nS and V(0)= +/- 34 mV. These results highlight unexpected differences between mCx26 and hCx26 in this expression system, reinforce the concept that channel permeability may be related to Cx level expression, and indicate that fusion of hCx30 to GFP colour mutants produces channels that are suitable for permeability and gating studies.


Subject(s)
Connexins/physiology , Ion Channel Gating , Animals , Cell Membrane Permeability , Connexin 26 , Connexin 30 , Connexins/genetics , Connexins/metabolism , Electric Conductivity , Fluorescent Dyes/chemistry , Fluorescent Dyes/metabolism , Gap Junctions/chemistry , Gap Junctions/physiology , Gene Expression , Green Fluorescent Proteins , HeLa Cells , Humans , Luminescent Proteins/genetics , Mice , Patch-Clamp Techniques , Recombinant Fusion Proteins/analysis , Transfection
8.
Biochem Biophys Res Commun ; 299(3): 424-31, 2002 Dec 06.
Article in English | MEDLINE | ID: mdl-12445818

ABSTRACT

Intercellular communication allows co-ordination of cell metabolism and sensitivity to extracellular stimuli. In bone cells, paracrine stimulation and cell-to-cell coupling through gap junctions induce the formation of complex intercellular networks, which favours the intercellular exchange of nutrients and second messengers, ultimately controlling the process of bone remodelling. The importance of local factors in bone remodelling is known since many years. Bone cells secrete and respond to a variety signals, among which include prostaglandins, cytokines, growth factors, and ATP. We here report evidence that extracellular NAD(+) is a novel extracellular signal stimulating osteoblast differentiation. We found that HOBIT human osteoblastic cells, which are known to express ADP-ribosyl cyclase/CD38 activity, respond to micromolar concentrations of extracellular NAD(+) with oscillatory increases of the cytosolic Ca(2+) concentration. The initial Ca(2+) response was followed by a time-dependent inhibition of cell growth, the appearance of an epithelial morphology, and by an increase of alkaline phosphatase and osteocalcin expression. Under resting condition HOBIT cells release NAD(+) in the extracellular medium and the release is significantly potentiated by mechanical stimulation. Taken together these results point to NAD(+) as a novel autocrine/paracrine factor involved in stimulation and maintenance of the osteoblast differentiated phenotype.


Subject(s)
Autocrine Communication/physiology , Fura-2/analogs & derivatives , NAD/metabolism , Osteoblasts/physiology , Paracrine Communication/physiology , Adult , Animals , Calcium/metabolism , Cell Division/physiology , Cell Line , Cell Size , Connexins/metabolism , Fluorescent Dyes/metabolism , Fura-2/metabolism , Humans , Intercellular Junctions/metabolism , Isoquinolines/metabolism , NAD/pharmacology , Osteoblasts/drug effects
9.
Biochem Biophys Res Commun ; 296(3): 685-91, 2002 Aug 23.
Article in English | MEDLINE | ID: mdl-12176036

ABSTRACT

Mutations in the GJB2 gene, encoding the gap-junction channel protein connexin 26, account for the majority of recessive forms and some of the dominant cases of deafness. Here, we report the frequency of GJB2 alleles in the Italian population affected by hearing loss and the functional analysis of six missense mutations. Genetic studies indicate that, apart from the common 35delG, only few additional mutations can be detected with a significant frequency in our population. Transfection of communication-incompetent HeLa cells with Cx26 missense mutations revealed three distinct classes of functional deficits in terms of protein expression, subcellular localisation and/or functional activity. Moreover, the M34T mutant acted as a dominant inhibitor of wild-type Cx26 channel activity when the two proteins were co-expressed in a manner mimicking a heterozygous genotype. These data support the hypothesis of a functional role for M34T as a dominant allele and represent a further step towards a complete understanding of the role of GJB2 in causing hearing loss.


Subject(s)
Connexins/genetics , Connexins/physiology , Deafness/genetics , Mutation , Alleles , Connexin 26 , Connexins/chemistry , Gene Frequency , HeLa Cells , Humans , Italy , Mutation, Missense , Protein Conformation
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