期刊论文详细信息
BMC Developmental Biology
Bioelectric patterning during oogenesis: stage-specific distribution of membrane potentials, intracellular pH and ion-transport mechanisms in Drosophila ovarian follicles
Johannes Bohrmann1  Julia Krüger1 
[1] RWTH Aachen University, Institut für Biologie II, Abt. Zoologie und Humanbiologie, Worringerweg 3, Aachen, 52056, Germany
关键词: Live-cell imaging;    Gap junction;    Ion pump;    Ion channel;    Membrane potential;    Pattern formation;    Cell communication;    Bioelectricity;    Oogenesis;    Drosophila melanogaster;   
Others  :  1089687
DOI  :  10.1186/s12861-015-0051-3
 received in 2014-09-28, accepted in 2015-01-05,  发布年份 2015
PDF
【 摘 要 】

Background

Bioelectric phenomena have been found to exert influence on various developmental and regenerative processes. Little is known about their possible functions and the cellular mechanisms by which they might act during Drosophila oogenesis. In developing follicles, characteristic extracellular current patterns and membrane-potential changes in oocyte and nurse cells have been observed that partly depend on the exchange of protons, potassium ions and sodium ions. These bioelectric properties have been supposed to be related to various processes during oogenesis, e. g. pH-regulation, osmoregulation, cell communication, cell migration, cell proliferation, cell death, vitellogenesis and follicle growth. Analysing in detail the spatial distribution and activity of the relevant ion-transport mechanisms is expected to elucidate the roles that bioelectric phenomena play during oogenesis.

Results

To obtain an overview of bioelectric patterning along the longitudinal and transversal axes of the developing follicle, the spatial distributions of membrane potentials (Vmem), intracellular pH (pHi) and various membrane-channel proteins were studied systematically using fluorescent indicators, fluorescent inhibitors and antisera. During mid-vitellogenic stages 9 to 10B, characteristic, stage-specific Vmem-patterns in the follicle-cell epithelium as well as anteroposterior pHi-gradients in follicle cells and nurse cells were observed. Corresponding distribution patterns of proton pumps (V-ATPases), voltage-dependent L-type Ca2+-channels, amiloride-sensitive Na+-channels and Na+,H+-exchangers (NHE) and gap-junction proteins (innexin 3) were detected. In particular, six morphologically distinguishable follicle-cell types are characterized on the bioelectric level by differences concerning Vmem and pHi as well as specific compositions of ion channels and carriers. Striking similarities between Vmem-patterns and activity patterns of voltage-dependent Ca2+-channels were found, suggesting a mechanism for transducing bioelectric signals into cellular responses. Moreover, gradients of electrical potential and pH were observed within single cells.

Conclusions

Our data suggest that spatial patterning of Vmem, pHi and specific membrane-channel proteins results in bioelectric signals that are supposed to play important roles during oogenesis, e. g. by influencing spatial coordinates, regulating migration processes or modifying the cytoskeletal organization. Characteristic stage-specific changes of bioelectric activity in specialized cell types are correlated with various developmental processes.

【 授权许可】

   
2015 Krüger and Bohrmann; licensee BioMed Central.

【 预 览 】
附件列表
Files Size Format View
20150127011502797.pdf 3332KB PDF download
Figure 8. 88KB Image download
Figure 7. 72KB Image download
Figure 6. 60KB Image download
Figure 5. 86KB Image download
Figure 4. 67KB Image download
Figure 3. 106KB Image download
Figure 2. 84KB Image download
Figure 1. 26KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

Figure 6.

Figure 7.

Figure 8.

【 参考文献 】
  • [1]McCaig CD, Rajnicek AM, Song B, Zhao M: Controlling cell behaviour electrically: current views and future potential. Physiol Rev 2005, 85:943-78.
  • [2]Zhao M, Song B, Pu J, Wada T, Reid B, Tai G, et al.: Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-gamma and PTEN. Nature 2006, 442:457-60.
  • [3]Levin M, Stevenson CG: Regulation of cell behavior and tissue patterning by bioelectric signals: challenges and opportunities for biomedical engineering. Annu Rev Biomed Eng 2012, 14:295-323.
  • [4]Campetelli A, Bonazzi D, Minc N: Electrochemical regulation of cell polarity and the cytoskeleton. Cytoskeleton 2012, 69:601-12.
  • [5]Overall R, Jaffe LF: Patterns of ionic currents through Drosophila follicles and eggs. Dev Biol 1985, 108:102-19.
  • [6]Bohrmann J, Dorn A, Sander K, Gutzeit H: The extracellular electrical current pattern and its variability in vitellogenic Drosophila follicles. J Cell Sci 1986, 81:189-206.
  • [7]Bohrmann J, Huebner E, Sander K, Gutzeit H: Intracellular electrical potential measurements in Drosophila follicles. J Cell Sci 1986, 81:207-21.
  • [8]Munley SM, Kinzeler S, Lizzano R, Woodruff RI: Fractional contribution of major ions to the membrane potential of Drosophila melanogaster oocytes. Arch Insect Biochem Physiol 2009, 70:230-43.
  • [9]Sun YA, Wyman RJ: Reevaluation of electrophoresis in the Drosophila egg chamber. Dev Biol 1993, 155:206-15.
  • [10]Spradling A: Developmental genetics of oogenesis. In The Development of Drosophila melanogaster. Edited by Bate M, Martinez Arias A. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York; 1993:1-70.
  • [11]Airoldi SJ, McLean PF, Shimada Y, Cooley L: Intercellular protein movement in syncytial Drosophila follicle cells. J Cell Sci 2011, 124:4077-86.
  • [12]Bohrmann J, Haas-Assenbaum A: Gap junctions in ovarian follicles of Drosophila melanogaster: inhibition and promotion of dye-coupling between oocyte and follicle cells. Cell Tissue Res 1993, 273:163-73.
  • [13]Ray RP, Schüpbach T: Intercellular signaling and the polarization of body axes during Drosophila oogenesis. Genes Dev 1996, 10:1711-23.
  • [14]González-Reyes A, St Johnston D: Patterning of the follicle cell epithelium along the anterior-posterior axis during Drosophila oogenesis. Development 1998, 125:2837-46.
  • [15]Grammont M, Irvine KD: Organizer activity of the polar cells during Drosophila oogenesis. Development 2002, 129:5131-40.
  • [16]Cavaliere V, Bernardi F, Romani P, Duchi S, Gargiulo G: Building up the Drosophila eggshell: first of all the eggshell genes must be transcribed. Dev Dyn 2008, 237:2061-72.
  • [17]Nishi T, Forgac M. The vacuolar (H+)-ATPases – nature’s most versatile proton pumps. Nat Rev Mol Cell Biol. 2002;3:94–103.
  • [18]Kawasaki-Nishi S, Nishi T, Forgac M: Proton translocation driven by ATP hydrolysis in V-ATPases. FEBS Lett 2003, 545:76-85.
  • [19]Nelson N: Organellar proton-ATPases. Curr Opin Cell Biol 1992, 4:654-60.
  • [20]Finbow ME, Harrison MA. The vacuolar H+-ATPase: a universal proton pump of eukaryotes. Biochem J. 1997;324:697–712.
  • [21]Wieczorek H: The insect V-ATPase, a plasma membrane proton pump energizing secondary active transport: molecular analysis of electrogenic potassium transport in the tobacco hornworm midgut. J Exp Biol 1992, 172:335-43.
  • [22]Harvey WR, Wieczorek H. Animal plasma membrane energization by chemiosmotic H+ V-ATPases. J Exp Biol. 1997;200:203–16.
  • [23]Pullikuth AK, Filippov V, Gill SS: Phylogeny and cloning of ion transporters in mosquitoes. J Exp Biol 2003, 206:3857-68.
  • [24]O´Donnell MJ, Sharda RK: Membrane potential and pH regulation in vitellogenic oocytes of an insect, Rhodnius prolixus. Physiol Zool 1994, 67:7-28.
  • [25]Wang Y, Telfer WH: Cyclic-AMP-induced water uptake in a moth ovary: inhibition by bafilomycin and anthracene-9-carboxylic acid. J Exp Biol 1998, 201:1627-35.
  • [26]Bohrmann J, Braun B: Na, K-ATPase and V-ATPase in ovarian follicles of Drosophila melanogaster. Biol Cell 1999, 91:85-98.
  • [27]Nuccitelli R: Endogenous electric fields in embryos during development, regeneration and wound healing. Radiat Prot Dosimetry 2003, 106:375-83.
  • [28]Levin M: Endogenous bioelectric networks store non-genetic patterning information during development and regeneration. J Physiol 2014, 592:2295-305.
  • [29]Adams DS, Robinson KR, Fukumoto T, Yuan S, Albertson RC, Yelick P, et al. Early, H+-V-ATPase-dependent proton flux is necessary for consistent left-right patterning of non-mammalian vertebrates. Development. 2006;133:1657–71.
  • [30]Cho MR, Thatte HS, Silvia MT, Golan DE: Transmembrane calcium influx induced by ac electric fields. FASEB J 1999, 13:677-83.
  • [31]Schuster A, Lacinová L, Klugbauer N, Ito H, Birnbaumer I, Hofmann F: The IV6 segment of the L-type calcium channel is critical for the action of dihydropyridines and phenylalkylamines. EMBO J 1996, 15:2365-70.
  • [32]Hockerman GH, Peterson BZ, Johnson BD, Catterall WA: Molecular determinants of drug binding and action on L-type calcium channels. Annu Rev Pharmacol Toxicol 1997, 37:361-96.
  • [33]Lee KS, Tsien RW: Mechanism of calcium channel blockade by verapamil, D600, diltiazem and nitrendipine in single dialysed heart cells. Nature 1983, 302:790-94.
  • [34]Rakotoarisoa L, Sayet I, Mironneau C, Mironneau J: Selective modulation by membrane potential of desmethoxyverapamil binding to calcium channels in rat portal vein. J Pharmacol Exp Ther 1990, 255:942-47.
  • [35]Armstrong CM, Hille B: Voltage-gated ion channels and electrical excitability. Neuron 1998, 20:371-80.
  • [36]Zhang MI, O´Neil RG: An L-type calcium channel in renal epithelial cells. J Membr Biol 1996, 154:259-66.
  • [37]MacPherson MR, Pollock VP, Broderick KE, Kean L, O´Connell FC, Dow JAT, et al.: Model organisms: new insights into ion channel and transport function. L-type calcium channels regulate epithelial fluid transport in Drosophila melanogaster. Am J Physiol Cell Physiol 2001, 280:394-407.
  • [38]Wakabayashi S, Shigekawa M, Pouyssegur J. Molecular physiology of vertebrate Na+/H+ exchangers. Physiol Rev. 1997;77:51–74.
  • [39]Giannakou ME, Dow JAT: Characterization of the Drosophila melanogaster alkali-metal/proton exchanger (NHE) gene family. J Exp Biol 2001, 204:3703-16.
  • [40]Kupitz Y, Atlas D. A putative ATP-activated Na+ channel involved in sperm-induced fertilization. Science. 1993;261:484–6.
  • [41]Darboux I, Lingueglia E, Champigny G, Coscoy S, Barbry P, Lazdunsky M. dGNaC1, a gonad-specific amiloride-sensitive Na+ channel. J Biol Chem. 1998;273:9424–9.
  • [42]Phelan P: Innexins: members of an evolutionarily conserved family of gap-junction proteins. Biochim Biophys Acta 2005, 1711:225-45.
  • [43]Bauer R, Löer B, Ostrowski K, Martini J, Weimbs A, Lechner H, et al.: Intercellular communication: the Drosophila innexin multiprotein family of gap junction proteins. Chem Biol 2005, 12:515-26.
  • [44]Barbe MT, Monyer H, Bruzzone R: Cell-cell communication beyond connexins: the pannexin channels. Physiology 2006, 21:103-14.
  • [45]Finbow ME, Pitts JD: Structure of the ductin channel. Biosci Rep 1998, 18:287-97.
  • [46]Bohrmann J: Antisera against a channel-forming 16 kDa protein inhibit dye-coupling and bind to cell membranes in Drosophila ovarian follicles. J Cell Sci 1993, 105:513-18.
  • [47]Bohrmann J, Lämmel H: Microinjected antisera against ductin affect gastrulation in Drosophila melanogaster. Int J Dev Biol 1998, 42:709-21.
  • [48]Bohrmann J, Bonafede A: Tissue-specific distribution and variation of the channel-forming protein ductin during development of Drosophila melanogaster. Int J Dev Biol 2000, 44:883-90.
  • [49]Stebbings LA, Todman MG, Phillips R, Greer CE, Tam J, Phelan P, et al.: Gap junctions in Drosophila: developmental expression of the entire innexin gene family. Mech Dev 2002, 113:197-205.
  • [50]Bohrmann J, Zimmermann J: Gap junctions in the ovary of Drosophila melanogaster: localization of innexins 1, 2, 3 and 4 and evidence for intercellular communication via innexin-2 containing channels. BMC Dev Biol 2008, 8:111. BioMed Central Full Text
  • [51]Robb JA: Maintenance of imaginal discs of Drosophila melanogaster in chemically defined media. J Cell Biol 1969, 41:876-85.
  • [52]Bohrmann J: In vitro culture of Drosophila ovarian follicles: the influence of different media on development, RNA synthesis, protein synthesis and potassium uptake. Rouxs Arch Dev Biol 1991, 199:315-26.
  • [53]Roth S, Lynch JA: Symmetry breaking during Drosophila oogenesis. Cold Spring Harb Perspect Biol 2009, 1:a001891.
  • [54]Leibfried A, Müller S, Ephrussi A: A Cdc42-regulated actin cytoskeleton mediates Drosophila oocyte polarization. Development 2013, 140:362-71.
  • [55]Viktorinová I, Dahmann C: Microtubule polarity predicts direction of egg chamber rotation in Drosophila. Curr Biol 2013, 23:1472-77.
  • [56]Grünert S, St Johnston D: RNA localization and the development of asymmetry during Drosophila oogenesis. Curr Opin Genet Dev 1996, 6:395-402.
  • [57]Dobens LL, Raftery LA: Integration of epithelial patterning and morphogenesis in Drosophila ovarian follicle cells. Dev Dyn 2000, 218:80-93.
  • [58]Jaffe LF: Organization of early development by calcium patterns. Bioessays 1999, 21:657-67.
  • [59]Créton R, Kreiling JA, Jaffe LF: Presence and roles of calcium gradients along the dorso-ventral axis in Drosophila embryos. Dev Biol 2000, 217:375-85.
  • [60]He L, Wang X, Tang HL, Montell DJ: Tissue elongation requires oscillating contractions of a basal actomyosin network. Nat Cell Biol 2010, 12:1133-42.
  • [61]Busa WB, Nuccitelli R: Metabolic regulation via intracellular pH. Am J Physiol 1984, 246:409-38.
  • [62]Madshus IH: Regulation of intracellular pH in eukaryotic cells. Biochem J 1988, 250:1-8.
  • [63]Simons M, Gault WJ, Gotthardt D, Rohatgi R, Klein TJ, Shao Y, et al.: Electrochemical cues regulate assembly of the Frizzled/Dishevelled complex at the plasma membrane during planar epithelial polarization. Nat Cell Biol 2009, 11:286-94.
  • [64]Giuliani F, Giuliani G, Bauer R, Rabouille C: Innexin 3, a new gene required for dorsal closure in Drosophila embryo. PLoS One 2013, 8:e69212.
  • [65]Bohrmann J, Heinrich U-R: Localisation of potassium pumps in Drosophila ovarian follicles. Zygote 1994, 2:189-99.
  • [66]Bohrmann J: Potassium uptake into Drosophila ovarian follicles: relevance to physiological and developmental processes. J Insect Physiol 1991, 37:937-46.
  • [67]Heinrich U-R, Gutzeit HO: Characterization of cation-rich follicle cells in vitellogenic follicles of Drosophila melanogaster. Differentiation 1985, 28:237-43.
  • [68]Stebbings LA, Todman MG, Phelan P, Bacon JP, Davies JA: Two Drosophila innexins are expressed in overlapping domains and cooperate to form gap-junction channels. Mol Biol Cell 2000, 11:2459-70.
  • [69]Dahl G, Muller KJ: Innexin and pannexin channels and their signaling. FEBS Lett 2014, 588:1396-402.
  • [70]Levin M: Molecular bioelectricity in developmental biology: new tools and recent discoveries. Bioessays 2012, 34:205-17.
  • [71]Yakoby N, Lembong J, Schüpbach T, Shvartsman SY: Drosophila eggshell is patterned by sequential action of feedforward and feedback loops. Development 2008, 135:343-51.
  • [72]Dahal GR, Rawson J, Gassaway B, Kwok B, Tong Y, Ptáček LJ, et al. An inwardly rectifying K+ channel is required for patterning. Development. 2012;139:3653–64.
  • [73]Adams DS, Levin M: Endogenous voltage gradients as mediators of cell-cell communication: strategies for investigating bioelectrical signals during pattern formation. Cell Tissue Res 2013, 352:95-122.
  文献评价指标  
  下载次数:44次 浏览次数:9次