Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
Add more filters










Publication year range
1.
Phys Med Biol ; 51(5): 1313-24, 2006 Mar 07.
Article in English | MEDLINE | ID: mdl-16481696

ABSTRACT

Diffraction enhanced imaging (DEI) uses refraction of x-rays at edges, which allows pronounced visualization of material borders and rejects scattering which often obscures edges and blurs images. Here, the first evidence is presented that, using DEI, a destruction-free evaluation of the quality of integration of metal implants into bone is possible. Experiments were performed in rabbits and sheep with model implants to investigate the option for DEI as a tool in implant research. The results obtained from DEI were compared to conventional histology obtained from the specimens. DE images allow the identification of the quality of ingrowth of bone into the hydroxyapatite layer of the implant. Incomplete integration of the implant with a remaining gap of less than 0.3 mm caused the presence of a highly refractive edge at the implant/bone border. In contrast, implants with bone fully grown onto the surface did not display a refractive signal. Therefore, the refractive signal could be utilized to diagnose implant healing and/or loosening.


Subject(s)
Bone Nails , Bone Remodeling , Radiographic Image Enhancement , Titanium/chemistry , Animals , Durapatite/chemistry , Femur/diagnostic imaging , Femur/physiology , Femur/surgery , Rabbits , Sheep/surgery , Tibia/diagnostic imaging , Tibia/physiology , Tibia/surgery , X-Ray Diffraction
2.
Bone ; 37(5): 699-710, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16139577

ABSTRACT

Osteointegration of metal implants into aged organisms can be severely compromised due to reduced healing capacity of bone, lack of precursor cells for new bone formation, or osteoporosis. Here, we report on successful implant healing in a novel model of aged sheep in the presence of nonglycosylated bone morphogenetic protein 2 (BMP-2). Ewes of 8 to 12 years with significant radiologic and histologic signs of osteoporosis and adipocytic bone marrow received a cylindrical hydroxyapatite-titanium implant of 12 x 10 mm. BMP-2 has been produced as a bacterial recombinant fusion protein with maltose-binding protein and in vitro generation of mature BMP-2 by renaturation and proteolytic cleavage. A BMP-2 inhibition ELISA was developed to measure the in vitro release kinetics of bioactive human BMP-2 from immersed solid implant materials by using Escherichia coli expressed and biotinylated recombinant human BMP-2 receptor IA extracellular domain (ALK-3 ECD). The implants were placed laterally below both tibial plateaus, with the left leg implant carrying 380 microg BMP-2. Both implant types became integrated within the following 20 weeks. The control implant only integrated at the cortical bone, and little new bone formation was found within the pre-existing trabecular bone or the marrow cavity. Marrow fat tissue was partially replaced by unspecific connective tissue. In contrast, BMP-2-coated implants initiated significant new bone formation, initially in trabecular arrangements to be replaced by cortical-like bone after 20 weeks. The new bone was oriented towards the cylinder. Highly viable bone marrow appeared and filled the lacunar structures of the new bone. In mechanical tests, the BMP-2-coated implants displayed in average 50% higher stability. This animal model provided first evidence that application of nonglycosylated BMP-2 coated on solid implants may foster bone healing and regeneration even in aged-compromised individuals.


Subject(s)
Aging , Bone Morphogenetic Proteins/physiology , Hydroxyapatites , Osseointegration , Osteogenesis/physiology , Prostheses and Implants , Titanium , Transforming Growth Factor beta/physiology , Animals , Biomechanical Phenomena , Bone Morphogenetic Protein 2 , Bone Morphogenetic Proteins/biosynthesis , Bone Morphogenetic Proteins/genetics , Bone Regeneration , Bone Remodeling , Disease Models, Animal , Female , Glycosylation , Models, Biological , Osteogenesis/genetics , Osteoporosis/metabolism , Osteoporosis/pathology , Osteoporosis/physiopathology , Recombinant Fusion Proteins , Sheep , Tibia/physiology , Transforming Growth Factor beta/biosynthesis , Transforming Growth Factor beta/genetics
3.
FEBS Lett ; 424(1-2): 63-8, 1998 Mar 06.
Article in English | MEDLINE | ID: mdl-9537516

ABSTRACT

Using the yeast two-hybrid system we isolated a cDNA clone encoding a novel protein interacting with the C-terminal domain of the 5-HT2C receptor. The protein, named MUPP1 (multi-PDZ-domain protein), contains thirteen PDZ domains and no obvious catalytic domain; it is related to hINADL and a putative C. elegans polypeptide referred to as C52A11.4 containing six or ten PDZ domains, respectively. Domains highly similar to those of MUPP1 are arrayed in the same order in all three proteins. The MUPP1 gene is localized on human chromosome 9p24-p22. Transcripts encoding MUPP1 are abundant in the brain as well as in several peripheral organs.


Subject(s)
Carrier Proteins/genetics , Carrier Proteins/isolation & purification , Receptors, Serotonin/genetics , Amino Acid Sequence , Animals , Brain/metabolism , Chromosome Mapping , DNA, Complementary/analysis , Humans , Intracellular Signaling Peptides and Proteins , Membrane Proteins , Molecular Sequence Data , Protein Conformation , RNA, Messenger/metabolism , Rats , Receptor, Serotonin, 5-HT2C , Receptors, Serotonin/chemistry , Sequence Alignment , Sequence Homology, Amino Acid
5.
Genomics ; 38(3): 435-7, 1996 Dec 15.
Article in English | MEDLINE | ID: mdl-8975724

ABSTRACT

Phospholipases A2 (PLA2) form an extended class of enzymes that play an important role in signal transduction. Phospholipase A2-like (PLA2L) belongs to the secreted forms of phospholipases A2, but constitutes a new subgroup. We have assigned the gene for this enzyme to human chromosome 8q24-qter using fluorescence in situ hybridization and radiation hybrid mapping techniques.


Subject(s)
Chromosomes, Human, Pair 8/genetics , Genes , Phospholipases A/genetics , Animals , Chromosome Mapping/methods , Chromosomes, Artificial, Yeast/genetics , Chromosomes, Human, Pair 8/radiation effects , DNA, Complementary/genetics , Humans , Hybrid Cells/radiation effects , Hybrid Cells/ultrastructure , In Situ Hybridization, Fluorescence , Phospholipases A2 , Schizophrenia/genetics
6.
Eur J Neurosci ; 8(5): 959-67, 1996 May.
Article in English | MEDLINE | ID: mdl-8743744

ABSTRACT

Several pharmaceuticals are frequently dispensed to prevent or reduce the occurrence of migraine attacks. The prophylactic effect of these drugs has been suggested to be caused through blockade of serotonin (5-HT) receptors of type 5-HT2B or 5-HT2C. To elucidate which of these receptors is involved, we first used radioligand binding assays to determine the pharmacological profile of the human and rat-5-HT2B receptor. Furthermore, the potency of drugs used in migraine prophylaxis to stimulate or inhibit 5-HT2B or 5-HT2C receptor-mediated potency of drugs used in migraine prophylaxis to stimulate or inhibit 5-HT2B or 5-HT2C receptor-mediated phosphatidyl inositol hydrolysis was measured. All these drugs were found to block both human receptors. Correlation of the receptor affinities with the potencies used in migraine prophylaxis showed significant correlations, which were better for the 5-HT2B (P = 0.001) than for the 5-HT2C receptor (P = 0.005). Migraine headache is thought to be transmitted by the trigeminal nerve from the meninges and their blood vessels. Using the reverse transcription-polymerase chain reaction, the expression patterns of all cloned G-protein-coupled serotonin receptors were analysed in various human meningeal tissues. All tissues expressed 5-HT1Dbeta, 5-HT2A, 5-HT2B, 5-HT4 and 5-HT7 mRNAs. Only trace amounts of 5-HT2C receptor mRNA were found. With organ bath experiments we showed that the 5-HT2B receptor stimulated the relaxation of the pig cerebral artery via the release of nitric oxide. Our data support the hypothesis that 5-HT2B receptors located on endothelial cells of meningeal blood vessels trigger migraine headache through the formation of nitric oxide.


Subject(s)
Meninges/drug effects , Migraine Disorders/prevention & control , Receptors, Serotonin/physiology , Serotonin Antagonists/pharmacology , Animals , Base Sequence , Cell Line , Cerebral Arteries/physiology , Humans , In Vitro Techniques , Meninges/metabolism , Migraine Disorders/physiopathology , Molecular Sequence Data , Polymerase Chain Reaction/methods , Rats , Time Factors , Transcription, Genetic , Vasodilation/physiology
7.
Br J Pharmacol ; 117(6): 1081-8, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8882600

ABSTRACT

1. We have characterized the 5-hydroxytryptamine (5-HT)-induced calcium signalling in endothelial cells from the human pulmonary artery. Using RT-PCR we show, that of all cloned G-protein coupled 5-HT receptors, these cells express only 5-HT1D beta, 5-HT2B and little 5-HT4 receptor mRNA. 2. In endothelial cells 5-HT inhibits the formation of adenosine 3':5'-cyclic monophosphate (cyclic AMP) via 5-HT1D beta receptors but fails to activate phosphoinositide (PI) turnover. However, the latter pathway is strongly activated by histamine. 3. Despite the lack of detectable inositol phosphate (IP) formation in human pulmonary artery endothelial cells, 5-HT (pD2 = 5.82 +/- 0.06, n = 6) or the selective 5-HT2 agonist, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI) (pD2 = 5.66 +/- 0.03, n = 7) elicited transient calcium signals comparable to those evoked by histamine (pD2 = 6.44 +/- 0.01, n = 7). Since 5-HT2A and 5-HT2C receptor mRNAs are not detectable in pulmonary artery endothelial cells, activation of 5-HT2B receptors is responsible for the transient calcium release. The calcium transients are independent of the inhibition of adenylate cyclase, since DOI does not stimulate 5-HT1D beta receptors. 4. Both, the 5-HT- and histamine-stimulated calcium signals were also observed when the cells were placed in calcium-free medium. This indicates that 5-HT triggers calcium release from intracellular stores. 5. Heparin is an inhibitor of the IP3-activated calcium release channels on the endoplasmic reticulum. Intracellular infusion of heparin through patch pipettes in voltage clamp experiments failed to block 5-HT-induced calcium signals, whereas it abolished the histamine response. This supports the conclusion that the 5-HT-induced calcium release is independent of IP3 formation. 6. Unlike the histamine response, the 5-HT response was sensitive to micromolar concentrations of ryanodine and, to a lesser extent, ruthenium red. This implies that 5-HT2B receptors trigger calcium release from a ryanodine-sensitive calcium pool. 7. It has been postulated that cyclic ADP-ribose (cADPR) is a soluble second messenger which activates ryanodine receptors. However, calcium signals similar to the 5-HT response could not be elicited by intracellular infusion with cADPR. Furthermore, the subsequent application of 5-HT or DOI elicited a calcium signal that was not affected by the above pretreatment. 8. We conclude that human 5-HT2B receptors stimulate calcium release from intracellular stores through a novel pathway, which involves activation of ryanodine receptors, and is independent of PI-hydrolysis and cADPR.


Subject(s)
Calcium/metabolism , Endothelium, Vascular/drug effects , Receptors, Serotonin/drug effects , Ryanodine/pharmacology , Serotonin/pharmacology , Cells, Cultured , Dose-Response Relationship, Drug , Endothelium, Vascular/metabolism , Histamine/pharmacology , Humans , Patch-Clamp Techniques , Pulmonary Artery/drug effects , Pulmonary Artery/metabolism , Receptor, Serotonin, 5-HT2B , Receptors, Serotonin/genetics , Receptors, Serotonin/metabolism , Ruthenium Red/pharmacology
8.
FEBS Lett ; 370(3): 215-21, 1995 Aug 21.
Article in English | MEDLINE | ID: mdl-7656980

ABSTRACT

Using RT-PCR we distinguished mRNAs for all known G-protein coupled serotonin receptors expressed in various rat and porcine blood vessels. Nearly all vessels expressed 5HT1D beta, 5-HT2A, 5-HT2B, 5-HT4, and 5-HT7 receptor mRNA to different extents. New splice variants of the porcine 5-HT4 receptor were observed. Similar PCR assays were performed with endothelial and smooth muscle cells from human pulmonary artery, aorta, and with endothelial cells from human coronary artery and umbilical vein. All endothelial cells expressed 5-HT1D beta, 5-HT2B, and 5-HT4 receptor mRNA, whereas in smooth muscle cells 5-HT1D beta, 5-HT2A, 5-HT7, and in some experiments 5-HT2B receptor mRNA were found. A model for the regulation of vascular tone by different 5-HT receptors is proposed.


Subject(s)
Blood Vessels/physiology , RNA, Messenger/analysis , Receptors, Serotonin/genetics , Amino Acid Sequence , Animals , Base Sequence , Blood Vessels/chemistry , Cells, Cultured , DNA, Complementary/chemistry , Endothelium, Vascular/cytology , Endothelium, Vascular/physiology , Gene Expression , Humans , Molecular Sequence Data , Muscle, Smooth/cytology , Muscle, Smooth/physiology , Polymerase Chain Reaction/methods , Rats , Sequence Homology, Amino Acid , Swine
9.
FEBS Lett ; 342(1): 85-90, 1994 Mar 28.
Article in English | MEDLINE | ID: mdl-8143856

ABSTRACT

Recently, we have reported the cloning of the rat 5-HT2B receptor cDNA. This receptor is particularly interesting since it may be involved in diseases such as migraine. Here, we describe the isolation of a human 5-HT2B receptor clone from a cDNA library derived from SH-SY5Y cells. Although the receptor sequence was only 80% homologous to the rat sequence, the exon-intron distribution was conserved between the two species. In the human body, the receptor mRNA was detected in most peripheral organs. Only low expression levels were found in the brain. After expression in HEK 293 cells, activation of the receptor stimulated the production of phosphatidylinositol. The pharmacology of this functional response correlated well with that of the rodent receptor.


Subject(s)
Cloning, Molecular , Receptors, Serotonin/genetics , Amino Acid Sequence , Animals , Base Sequence , Cell Line , DNA, Complementary/genetics , DNA, Complementary/isolation & purification , Exons , HeLa Cells , Humans , Introns , Mice , Molecular Sequence Data , Phosphatidylinositols/metabolism , Rats , Receptors, Serotonin/chemistry , Receptors, Serotonin/metabolism , Second Messenger Systems , Sequence Alignment , Serotonin/pharmacology , Serotonin Antagonists/pharmacology
10.
EMBO J ; 12(3): 903-10, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8384555

ABSTRACT

Serotonergic neurons located at the base of the mammalian brain innervate practically every region of the brain and the spinal cord. These neurons exhibit spontaneous electrical discharges in a rhythmical way. Their firing frequency is modulated by serotonin autoreceptors which also regulate intracellular cAMP levels. We have investigated how elevated levels of cAMP alter the development and the functional properties of serotonergic neurons in culture. To study the influence of cAMP on the expression of genes underlying serotonergic activity, a quantitative RT-PCR approach using internal standards was developed. Cultures of embryonic rat brain serotonergic neurons were continuously treated with cAMP analogues. Increased cAMP levels had three effects. First, the neuronal morphology was changed towards that typical for mature serotonergic neurons. Second, the expression of tryptophan hydroxylase, the rate-limiting enzyme in serotonin production, was increased in dibutyryl-cAMP treated cultures. Third, the expression of the inhibitory autoreceptor (5-HT1A) was down-regulated. These results suggest the existence of a mechanism by which the neurons react to synaptic input regulating intracellular cAMP levels. Increased cAMP concentrations affect the development and cause a prolonged activation of serotonergic transmission. Since 5-HT1A receptors inhibit cAMP formation, their down-regulation argues against a negative feedback control in this system, consistent with observations in vivo.


Subject(s)
Neurons/metabolism , Protein Kinases/metabolism , Raphe Nuclei/metabolism , Serotonin/metabolism , Animals , Base Sequence , Bucladesine/pharmacology , Cells, Cultured , DNA , Enzyme Activation , Gene Expression/drug effects , Molecular Sequence Data , Neurons/drug effects , Polymerase Chain Reaction , Raphe Nuclei/cytology , Raphe Nuclei/drug effects , Raphe Nuclei/enzymology , Rats , Rats, Sprague-Dawley , Receptors, Serotonin/genetics , Serotonin/genetics , Tryptophan Hydroxylase/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...