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Marinova Z Vukojevic V Surcheva S Yakovleva T Cebers G Pasikova N Usynin I Hugonin L Fang W Hallberg M Hirschberg D Bergman T Langel U Hauser KF Pramanik A Aldrich JV Gräslund A Terenius L Bakalkin G 《The Journal of biological chemistry》2005,280(28):26360-26370
Several peptides, including penetratin and Tat, are known to translocate across the plasma membrane. Dynorphin opioid peptides are similar to cell-penetrating peptides in a high content of basic and hydrophobic amino acid residues. We demonstrate that dynorphin A and big dynorphin, consisting of dynorphins A and B, can penetrate into neurons and non-neuronal cells using confocal fluorescence microscopy/immunolabeling. The peptide distribution was characterized by cytoplasmic labeling with minimal signal in the cell nucleus and on the plasma membrane. Translocated peptides were associated with the endoplasmic reticulum but not with the Golgi apparatus or clathrin-coated endocytotic vesicles. Rapid entry of dynorphin A into the cytoplasm of live cells was revealed by fluorescence correlation spectroscopy. The translocation potential of dynorphin A was comparable with that of transportan-10, a prototypical cell-penetrating peptide. A central big dynorphin fragment, which retains all basic amino acids, and dynorphin B did not enter the cells. The latter two peptides interacted with negatively charged phospholipid vesicles similarly to big dynorphin and dynorphin A, suggesting that interactions of these peptides with phospholipids in the plasma membrane are not impaired. Translocation was not mediated via opioid receptors. The potential of dynorphins to penetrate into cells correlates with their ability to induce non-opioid effects in animals. Translocation across the plasma membrane may represent a previously unknown mechanism by which dynorphins can signal information to the cell interior. 相似文献
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Ugo Mellone Pascual López‐López Rubén Limiñana Gvido Piasevoli Vicente Urios 《Journal of avian biology》2013,44(5):417-426
Internal factors such as experience (e.g. age) and motivation for breeding, and external ones such as environmental conditions (e.g. meteorology and landscape characteristics) can promote differences in migratory behaviour and routes among seasons, regions and populations. Using satellite telemetry we investigated whether such differences occur and which factors promote them among migrating Eleonora’s falcons breeding in the Mediterranean area (Spain and Croatia) and wintering in Madagascar. We found that during autumn migration no age differences occur when crossing the Sahara desert, but in the remaining African regions, juveniles were more prone than adults to fly at a slower and more tortuous rate, as well as exhibiting longer stop‐overs, particularly in the Sahel region. Such differences might be promoted by a lower foraging and pre‐migratory fattening efficiency in juveniles. During spring, routes were significantly more eastern than during autumn, resulting in a loop migration occurring in all studied populations. This could be accounted by seasonal variation in the distribution of trophic resources. Our results show that Eleonora’s falcons integrate spatially seasonal changing resources on a continental scale throughout their annual cycle, changing their movement patterns in response to internal (age) and external (habitat) factors. This loop migration pattern may prove to be widespread among other Palearctic trans‐continental migratory bird species. 相似文献
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Ann Hjelm Cluff Birgitta Byström Aurelija Klimaviciute Camilla Dahlqvist Gvido Cebers Anders Malmström Gunvor Ekman-Ordeberg 《Reproductive biology and endocrinology : RB&E》2006,4(1):24-9
Background
Prolonged labour is associated with greater morbidity and mortality for mother and child. Connexin 43 is a major myometrial gap junction protein found in human myometrium. Syndecan 3 seems to prevail in the human uterus among heparan sulphate proteoglycans, showing the most significant increase during labour. The aims of the present study were to investigate syndecan 3 and connexin 43 mRNA expressions and protein distributions in human uterine tissue during normal and prolonged labour. 相似文献
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