scholarly journals A highly polarized excitable cell separates sodium channels from sodium-activated potassium channels by more than a millimeter

2015 ◽  
Vol 114 (1) ◽  
pp. 520-530 ◽  
Author(s):  
Yue Ban ◽  
Benjamin E. Smith ◽  
Michael R. Markham

The bioelectrical properties and resulting metabolic demands of electrogenic cells are determined by their morphology and the subcellular localization of ion channels. The electric organ cells (electrocytes) of the electric fish Eigenmannia virescens generate action potentials (APs) with Na+ currents >10 μA and repolarize the AP with Na+-activated K+ (KNa) channels. To better understand the role of morphology and ion channel localization in determining the metabolic cost of electrocyte APs, we used two-photon three-dimensional imaging to determine the fine cellular morphology and immunohistochemistry to localize the electrocytes' ion channels, ionotropic receptors, and Na+-K+-ATPases. We found that electrocytes are highly polarized cells ∼1.5 mm in anterior-posterior length and ∼0.6 mm in diameter, containing ∼30,000 nuclei along the cell periphery. The cell's innervated posterior region is deeply invaginated and vascularized with complex ultrastructural features, whereas the anterior region is relatively smooth. Cholinergic receptors and Na+ channels are restricted to the innervated posterior region, whereas inward rectifier K+ channels and the KNa channels that terminate the electrocyte AP are localized to the anterior region, separated by >1 mm from the only sources of Na+ influx. In other systems, submicrometer spatial coupling of Na+ and KNa channels is necessary for KNa channel activation. However, our computational simulations showed that KNa channels at a great distance from Na+ influx can still terminate the AP, suggesting that KNa channels can be activated by distant sources of Na+ influx and overturning a long-standing assumption that AP-generating ion channels are restricted to the electrocyte's posterior face.

Author(s):  
Junjie Quan ◽  
Enze Xu ◽  
Hanwen Zhu ◽  
Yajing Chang ◽  
Yi Zhu ◽  
...  

Prussian blue analogues are potential competitive energy storage materials due to its diverse metal combinations and wide three-dimensional ion channels. Here, we prepared a new high crystalline monoclinic nickel doped...


1987 ◽  
Vol 105 (1) ◽  
pp. 387-395 ◽  
Author(s):  
J A Traas ◽  
J H Doonan ◽  
D J Rawlins ◽  
P J Shaw ◽  
J Watts ◽  
...  

We have studied the F-actin network in cycling suspension culture cells of carrot (Daucus carota L.) using rhodaminyl lysine phallotoxin (RLP). In addition to conventional fixation with formaldehyde, we have used two different nonfixation methods before adding RLP: extracting cells in a stabilizing buffer; inducing transient pores in the plasma membrane with pulses of direct current (electroporation). These alternative methods for introducing RLP revealed additional features of the actin network not seen in aldehyde-fixed cells. The three-dimensional organization of this network in nonflattened cells was demonstrated by projecting stereopairs derived from through-focal series of computer-enhanced images. F-actin is present in interphase cells in four interconnected configurations: a meshwork surrounding the nucleus; thick cables in transvacuolar strands and deep in the cytoplasm; a finer network of bundles within the cortical cytoplasm; even finer filaments that run in ordered transverse array around the cell periphery. The actin network is organized differently during division but it does not disappear as do the cortical microtubules. RLP stains a central filamentous cortical band as the chromatin begins to condense (preprophase); it stains the mitotic spindle (as recently shown by Seagull et al. [Seagull, R. W., M. Falconer, and C. A. Weerdenburg, 1987, J. Cell Biol., 104:995-1004] for aldehyde fixed suspension cells) and the cytokinetic apparatus (as shown by Clayton, L., and C. W. Lloyd, 1985, Exp. Cell Res., 156:231-238). However, it is now shown that an additional network of F-actin persists in the cytoplasm throughout division associating in turn with the preprophase band, the mitotic spindle, and the cytokinetic phragmoplast.


Author(s):  
Jean Uhlendorf ◽  
Carolina A. Cartelli ◽  
Larissa C. Trojan ◽  
Geninho Thomé ◽  
Marcos B. Moura

Immediate loading of full-arch prostheses on dental implants in the upper arch is challenging, as the bone is of low quality and obtaining sufficient torque may be difficult. The purpose of this case report is to describe the rehabilitation of a full-arch by means of placement of four internal tapered connection tilted implants and immediate loading. A 65-year-old man sought dental care with a partially edentulous upper arch. The teeth presented mobility and were extracted. In a second step, two conventional-length implants were placed in the anterior region and two tilted and nasal wall–directed extra-long implants in the posterior region. The insertion torques of 60 N.cm allowed the installation of an immediate prosthesis (hybrid). The clinical case report suggests that the placement of tilted and extra-long implants in the paranasal bone and immediate loading may be a viable option for rehabilitation of the edentulous upper arch.


2017 ◽  
Vol 43 ◽  
pp. 221-251 ◽  
Author(s):  
Riccardo Sacco ◽  
Paolo Airoldi ◽  
Aurelio G. Mauri ◽  
Joseph W. Jerome

1928 ◽  
Vol s2-72 (287) ◽  
pp. 447-483
Author(s):  
C. J. GEORGE

1. In the male Philaenus and Agrion the vasa deferentia terminate on the ninth segment in the early stages. An ectodermal invagination from that segment joins them subsequently and thus the male gonopore is established. 2. The accessory glands develop in Philaenus male from the anterior end of the swollen extremities of the vasa deferentia and the vesiculae seminales from a still more forward region. 3. The accessory glands of the male are mesodermal in origin and not ectodermal as some authors state. 4. There is no evidence as to the existence of a ‘pair of ectodermal ejaculatory’ ducts either in Philaenus orin Agrion, and reasons are adduced to show that they do not exist at all in the higher Insecta. 5. In the female nymph of Philaenus the oviducts terminate on the seventh segment. They are subsequently joined by an ectodermal invagination from the seventh segment. The common oviduct is formed in two parts: the anterior part is derived from the posterior region of the invagination on the seventh and the posterior region is formed as a groove from the ectodermis of the eighth segment and subsequently this groove is converted into a tube. When the second part is completed it is in connexion with the invagination from the seventh and opens to the outside on the eighth segment. The ectodermal invagination from the seventh also gives rise to the spermatheca. A median accessory gland develops as an invagination from the ninth segment between the bases of the inner ovipositor lobes. A pair of accessory glands develop as paired imaginations from the anterior region of the ninth segment. 6. In the female nymph of Agrion the oviducts fuse to form a single duct and terminate in the middle of the eighth segment. Posteriorly an ectodermal invagination from the eighth segment meets this duct and lies in a position dorsal to it. Later on the ectodermal invagination develops a spermatheca dorsally and the mesodermal and the ectodermal ducts unite into one. The accessory glands develop as paired ectodermal invaginations from the anterior region of the ninth segment. 7. The female gonopore is not homologous in the different groups of insects. The vaginal opening in Orthoptera, Hymenoptera, Homoptera, Diptera, and Lepidoptera is homologous. The vaginal opening in Coleoptera is homologous with the oviducal opening of Lepidoptera, with the opening of the accessory gland of Homoptera, Hymenoptera, Diptera, Isoptera, and the opening of the spermatheca in some Orthoptera. 8. The common oviduct, being formed differently in the different groups is not homologous. The accessory organs, e. g. spermatheca, are not homologous in the different groups. 9. There is no evidence to show that the common oviduct is of paired origin. 10. The occurrence of a median accessory structure on the ninth segment which develops in the young as an invagination between the bases of the inner ovipositor lobes is very general in the higher Insecta. In some it functions as a gland, in others as a storehouse for spermatozoa. 11. The homology of the paired accessory glands is indicated. 12. The male genital ducts are not strictly homologous with those of the female. The homologue of the ejaculatory duct is the invagination from the ninth segment in the female. 13. The Odonata stand isolated in having a mesodermal region for the common oviduct and in the peculiar development of the two processes between the anterior ovipositor lobes. 14. The probable lines of evolution of the female efferent system in Insecta are indicated. The study of the development of the female efferent system indicates that the groups Orthoptera, Homoptera, Lepidoptera, and Diptera are very closely allied. Coleoptera seem to have had quite a different line of evolution from the above groups in this respect. 15. The adult Odonatan anatomy of the genital organs in the female as observed by me is in some respects different from that described by Tillyard. In conclusion I wish to express my deep sense of gratitude towards Professor Balfour-Browne and Dr. J. W. Munroe, both of whom have always been ready to help me. My colleague Mr. R. I. Nel, who is working on similar lines in this department,, has rendered me valuable help, not only in matters connected with the subject proper but also in translating difficult German references. I am also indebted to Mr. Peter Gray who helped me a good deal in translating references in Italian.


Development ◽  
1979 ◽  
Vol 53 (1) ◽  
pp. 75-90
Author(s):  
Elizabeth L. Wee ◽  
Bruce S. Babiarz ◽  
Stephen Zimmerman ◽  
Ernest F. Zimmerman

Previous studies have localized non-muscle contractile systems in the posterior (region 2) and the anterior (region 3) ends of mouse palates at the time of shelf movement. In order to determine whether these contractile systems function in shelf rotation, effects of pharmacologic agents have been analyzed in embryo culture. First, it was shown that the posterior end of the palate rotates before the anterior end, and its rotation in culture was proportionally greater as development of the embryo progressed. Generally, the posterior end of the palate was more easily inhibited in embryo culture than the anterior end. Serotonin at 10–−8 M to 10–−5 M was shown to significantly stimulate rotation atthe anterior end of the palate after 2 h in embryo culture. The effect on the posterior palate was less pronounced. To investigate further the role of this neurotransmitter on palate shelf rotation, serotonin antagonists were employed. Methysergide (10–−4 M) inhibited anterior shelf rotation to 12% of control values (P < 0·005), while not significantly affecting the posterior end. Ergotamine (10–−6 M) significantly inhibited the stimulation induced by 10–−5 M serotonin (P < 0·025). Cyproheptadine (10–−9 M) partially inhibited anterior and posterior shelf rotation in embryo culture. When injected into the pregnant dam, cyproheptadine partially inhibited shelf rotation and fusion. The palate was examined histologically after embryo culture. In the presence of 10–−4 M methysergide, the elongated contractile cells in region 3 at the anterior and midpalatal mesenchyme were prevented from rounding. Thus, serotonin may be regulating rotation of the anterior end of the palate by an effect on a cell-mediated process.


2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Takayuki Yoshida ◽  
Yoshiko Watanabe ◽  
Takeshi Hashimoto ◽  
Atsushi Ohta ◽  
Tatsuo Nakamoto

Single injections in the anterior region of the thoracic paravertebral space (TPVS) have been reported to generate a multisegmental longitudinal spreading pattern more frequently than those in the posterior region of the TPVS. In this trial, we examined the hypothesis that a continuous thoracic paravertebral block (TPVB) administered through a catheter inserted into the anterior region of the TPVS allows a wider sensory block dispersion. Fifty consecutive patients undergoing video-assisted thoracic surgery were enrolled. Before the surgery, an infusion catheter was inserted into the TPVS through a needle placed adjacent to either the parietal pleura (group A) or internal intercostal membrane (group P) using an ultrasound-guided intercostal transverse approach according to a randomized allocation schedule. A chest radiograph was obtained postoperatively after injection of 10 mL of radiopaque dye through the catheter. Thereafter, 20 mL of 0.375% levobupivacaine was injected via the catheter, followed by commencement of continuous TPVB with 0.25% levobupivacaine at 8 mL/h. The primary outcome was the number of blocked dermatomes at 24 h after surgery. The secondary outcomes included radiopaque dye spreading patterns, the number of segments reached by the radiopaque dye, the number of blocked dermatomes at 2 h after surgery, and pain scores. The median (interquartile range [range]) number of blocked dermatomes 24 h after surgery was 3 (2.75–4 [1–6]) in group A (n = 22) and 2 (1.5–3 [0–7]) in group P (n = 25; p = 0.037). No significant differences in the other outcomes were found between the groups. In conclusion, a continuous TPVB administered using a catheter supposedly inserted into the anterior region of the TPVS allows a wider sensory block dispersion than a catheter inserted into the posterior region of the TPVS. This trial is registered with the UMIN Clinical Trials Registry (UMIN000018578).


2015 ◽  
Vol 126 (8) ◽  
pp. e79
Author(s):  
P. Broser ◽  
R. Beschroner ◽  
M. Ginger ◽  
S. Rona ◽  
M. Schuhmann ◽  
...  

1982 ◽  
Vol 56 (1) ◽  
pp. 453-460
Author(s):  
K. Mikami

Nuclear differentiation in exconjugants of Paramecium caudatum is closely associated with a brief localization of the postzygotic nuclei near the opposite ends of the cell, with the germinal nucleus (micronucleus) in the anterior region and the somatic nuclei (macronuclei) in the posterior region. The posterior nuclei cannot regenerate to produce micronuclei when all four anterior nuclei are removed. There is no difference among the anterior four presumptive micronuclei, because, when any three of them were removed, the remaining nucleus was able to divide at each postconjugational fission and to persist as a micronucleus during the vegetative phase. This conclusion agrees with the results of transplanting a presumptive micronucleus into a vegetative cell. Cells during the vegetative phase, however, normally have only one micronucleus. Micronuclear number must be reduced to arrive at the uni-micronucleate condition after the stage of macro- and micronuclear differentiation. Elimination of supernumerary presumptive micronuclei, which had been indicated by morphological observations, was confirmed by the results of nuclear transplantation studies.


2014 ◽  
Vol 307 (3) ◽  
pp. C255-C265 ◽  
Author(s):  
Agnieszka K. Dymowska ◽  
Aaron G. Schultz ◽  
Salvatore D. Blair ◽  
Danuta Chamot ◽  
Greg G. Goss

A role for acid-sensing ion channels (ASICs) to serve as epithelial channels for Na+ uptake by the gill of freshwater rainbow trout was investigated. We found that the ASIC inhibitors 4′,6-diamidino-2-phenylindole and diminazene decreased Na+ uptake in adult rainbow trout in a dose-dependent manner, with IC50 values of 0.12 and 0.96 μM, respectively. Furthermore, we cloned the trout ASIC1 and ASIC4 homologs and demonstrated that they are expressed differentially in the tissues of the rainbow trout, including gills and isolated mitochondrion-rich cells. Immunohistochemical analysis using custom-made anti-zASIC4.2 antibody and the Na+-K+-ATPase (α5-subunit) antibody demonstrated that the trout ASIC localizes to Na+/K+-ATPase-rich cells in the gill. Moreover, three-dimensional rendering of confocal micrographs demonstrated that ASIC is found in the apical region of mitochondrion-rich cells. We present a revised model whereby ASIC4 is proposed as one mechanism for Na+ uptake from dilute freshwater in the gill of rainbow trout.


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