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971.
972.
Ruggiero M Bottaro DP Liguri G Gulisano M Peruzzi B Pacini S 《Bioelectromagnetics》2004,25(5):390-396
Inhibition of angiogenesis is a major target in the fight against cancer and other diseases. Although the effects of static magnetic fields on cancer development and cell growth have been investigated, effects on angiogenesis have received no attention so far. In this study we report the effects on angiogenesis of exposure to 0.2 T static magnetic field. Angiogenesis was analyzed using the chick embryo chorioallantoic membrane assay. Exposure to 0.2 T static magnetic field was achieved by placing the eggs for 3 hr in the isocentre of the magnet of a sectorial magnetic resonance tomograph used in clinical practice. In sham exposed specimens treated with phosphate buffered saline (negative control), no significant vascular reaction was detectable; 3 hr exposure to 0.2 T static magnetic field did not affect the basal pattern of vascularization or chick embryo viability. Prostaglandin E1 and fetal calf serum elicited a strong angiogenic response in sham exposed eggs. This angiogenic response was significantly inhibited by 3 hr exposure to 0.2 T static magnetic field. These findings point to possible use of static magnetic field in inhibiting angiogenesis; this effect could be exploited for treatment of cancer and other diseases where excessive angiogenesis is involved. 相似文献
973.
Viard M Parolini I Rawat SS Fecchi K Sargiacomo M Puri A Blumenthal R 《Glycoconjugate journal》2004,20(3):213-222
Although HIV uses CD4 and coreceptors (CCR5 and CXCR4) for productive infection of T cells, glycosphingolipids (GSL) may play ancillary roles in lymphoid and non-lymphoid cells. Interactions of the HIV Envelope Glycoprotein (Env) with GSL may help HIV in various steps of its pathogenesis. Physical-chemical aspects of the interactions between HIV Env and GSL leading to CD4-dependent entry into lymphocytes, the role of GSL in HIV transcytosis, and CD4-independent entry into non-lymphoid cells are reviewed. An overview of signaling properties of HIV receptors is provided with some speculation on how GSL may play a role in these events by virtue of being in membrane rafts. Finally, we summarize how interactions between HIV and coreceptors leading to signaling and/or fusion can be analyzed by the use of various tyrosine kinase and cytoskeletal inhibitors. 相似文献
974.
Integrin-linked kinase regulates endothelial cell survival and vascular development 总被引:9,自引:0,他引:9
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Friedrich EB Liu E Sinha S Cook S Milstone DS MacRae CA Mariotti M Kuhlencordt PJ Force T Rosenzweig A St-Arnaud R Dedhar S Gerszten RE 《Molecular and cellular biology》2004,24(18):8134-8144
Integrin-linked kinase (ILK) is a phosphoinositide 3-kinase-dependent serine/threonine kinase that interacts with beta integrins. Here we show that endothelial cell (EC)-specific deletion of ILK in mice confers placental insufficiency with decreased labyrinthine vascularization, yielding no viable offspring. Deletion of ILK in zebra fish using antisense morpholino oligonucleotides results in marked patterning abnormalities of the vasculature and is similarly lethal. To dissect potential mechanisms responsible for these phenotypes, we performed ex vivo deletion of ILK from purified EC of adult mice. We observed downregulation of the active-conformation of beta1 integrins with a striking increase in EC apoptosis associated with activation of caspase 9. There was also reduced phosphorylation of the ILK kinase substrate, Akt. However, phenotypic rescue of ILK-deficient EC by wild-type ILK, but not by a constitutively active mutant of Akt, suggests regulation of EC survival by ILK in an Akt-independent manner. Thus, endothelial ILK plays a critical role in vascular development through integrin-matrix interactions and EC survival. These data have important implications for both physiological and pathological angiogenesis. 相似文献
975.
Pomponi M Gavuzzo E Bertonati C Derocher AE Lydersen C Wiig Ø Kovacs KM 《Biochimie》2004,86(12):927-932
In this study a decreased DPG response by polar bear (Ursus maritimus) hemoglobin was observed, and this response was interpreted as an example of gradual DPG/chloride shifting. This sort of mechanism has been suggested to occur in ruminants and, intuitively, one might guess that for ruminants the DPG/Cl- shifting might have been beneficial and hence selected for at the time of the latest Ice Age. However, suggestion that this is purely a temperature effect in polar bears and ruminants conflicts with the existence, in the hot savanna, of mammals that have Hb modulated by chloride. However, acidosis effects caused by routine periods of food shortage, induced in extreme environments may explain the responses of the hemoglobins of animals adapted to extreme habitats. The chloride effect is bound to specific amino acid substitutions in key positions. In polar bear Hb, they are specific, additional (with respect to human HbA) O2-linked chloride binding sites located between Lys-76 (beta) and Lys-8 (beta). The amino acids operate as an additional H+ binding site for a chloride anion. Additionally, with respect to human adult HbA, the primary structure of polar bear Hb was characterized by two substitutions in beta chains: Pro-5 (A2)--> Gly and Ala-76 (E20)-->Lys. The increased flexibility of the A helix causes the lower DPG effect. We further hypothesize that the resulting widening of the central cavity allows the Lys-82 (beta) terminus to be free and constitute an additional, chloride-binding site. 相似文献
976.
977.
Monticelli A Giacchetti M De Biase I Pianese L Turano M Pandolfo M Cocozza S 《Human genetics》2004,114(5):458-463
Friedreichs ataxia (FRDA) is an autosomal recessive neurodegenerative disorder commonly caused by large expansions of a GAA repeat in the first intron of the frataxin gene, FRDA. The expansion of the triplet repeat is localized within an Alu sequence. FRDA GAA-repeat alleles can be divided into three classes depending on their lengths: short normal alleles (SN), long normal alleles (LN) and expanded pathological alleles (E). We made an accurate analysis of the Alu sequence containing the GAA repeat. We found a new single-nucleotide polymorphism (SNP) that is the closest one to the GAA repeat. We studied this new SNP and the polymorphic polyA region contiguous to the GAA triplets in two populations with different frequencies of FRDA. We found that, while both E and LN alleles seem to be genetically homogeneous and likely related, SN represents a more heterogeneous class of alleles. Indeed, one SNP variation (T) was more frequently associated with (GAA)8 alleles, whereas the other one (C) with (GAA)9 repeat(s). The long normal and expanded alleles presented the C haplotype. The same correlation was described for polyA-tract polymorphisms. Thus, 14A was commonly associated with (GAA)8 alleles and 17A with (GAA)9 alleles. The long normal alleles more frequently showed the 17A haplotype. Our data seem to suggest that all the E alleles come from LN alleles, while LN alleles come from a defined subclass of SN alleles. 相似文献
978.
979.
Bonecchi R Locati M Galliera E Vulcano M Sironi M Fra AM Gobbi M Vecchi A Sozzani S Haribabu B Van Damme J Mantovani A 《Journal of immunology (Baltimore, Md. : 1950)》2004,172(8):4972-4976
The promiscuous D6 receptor binds several inflammatory CC chemokines and has been recently proposed to act as a chemokine-scavenging decoy receptor. The present study was designed to better characterize the spectrum of CC chemokines scavenged by D6, focusing in particular on CCR4 ligands and analyzing the influence of NH(2)-terminal processing on recognition by this promiscuous receptor. Using D6 transfectants, it was found that D6 efficiently bound and scavenged most inflammatory CC chemokines (CCR1 through CCR5 agonists). Homeostatic CC chemokines (CCR6 and CCR7 agonists) were not recognized by D6. The CCR4 agonists CC chemokine ligand 17 (CCL17) and CCL22 bound to D6 with high affinity. CCL17 and CCL22 have no agonistic activity for D6 (chemotaxis and calcium fluxes), but were rapidly scavenged, resulting in reduced chemotactic activity on CCR4 transfectants. CD26 mediates NH(2) terminus processing of CCL22, leading to the production of CCL22 (3-69) and CCL22 (5-69) that do not interact with CCR4. These NH(2)-terminal truncated forms of CCL22 were not recognized by D6. The results presented in this study show that D6 recognizes and scavenges a wide spectrum of inflammatory CC chemokines, including the CCR4 agonists CCL22 and CCL17. However, this promiscuous receptor is not engaged by CD26-processed, inactive, CCL22 variants. By recognizing intact CCL22, but not its truncated variants, D6 expressed on lymphatic endothelial cells may regulate the traffic of CCR4-expressing cells, such as dendritic cells. 相似文献
980.
Cousens C Bishop JV Philbey AW Gill CA Palmarini M Carlson JO DeMartini JC Sharp JM 《Journal of virology》2004,78(16):8506-8512
Ovine pulmonary adenocarcinoma (OPA) is an infectious lung tumor of sheep caused by Jaagsiekte sheep retrovirus (JSRV). To test the hypothesis that JSRV insertional mutagenesis is involved in the oncogenesis of OPA, we cloned and characterized 70 independent integration sites from 23 cases of OPA. Multiple integration sites were identified in most tumors. BLAST analysis of the sequences did not disclose any potential oncogenic motifs or any identical integration sites in different tumors. Thirty-seven of the integration sites were mapped to individual chromosomes by PCR with a panel of sheep-hamster hybrid cell lines. Integration sites were found on 20 of the 28 sheep chromosomes, suggesting a random distribution. However, four integration sites from four different tumors mapped to chromosome 16. By Southern blot hybridization, probes derived from two of these sites mapped to within 5 kb of each other on normal sheep DNA. These sites were found within a single sheep bacterial artificial chromosome clone and were further mapped to only 2.5 kb apart, within an uncharacterized predicted gene and less than 200 kb from a mitogen-activated protein kinase-encoding gene. These findings suggest that there is at least one common integration site for JSRV in OPA and add weight to the hypothesis that insertional mutagenesis is involved in the development of this tumor. 相似文献