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Development & Regeneration

Xenopus oocytes

Embryonic development through to the birth of a healthy child is without doubt one of biology's most startling achievements and one we tend to take for granted. The process is immensely complex and much remains to be learned about the basic underlying mechanism and its rare, but painful, failure. In some cases, such as neural tube defects in diabetic pregnancy, a cause can be delineated (Click here for related BRC study). In others, such as Hypoplastic Left Heart Syndrome, which affects 1 in 8000 births, basic research is still required to understand the process and its error.

Historically the study of development and polarity has been a driving force behind a number of the technologies currently available and advanced through the BRC. Unequal, patterned and polarized electric fields, working in their own right or through their constituent flux of charged ions, have been recognized as real or potential mechanisms in developmental control. 6 The roles of calcium as regulating waves and second messenger events have formed key areas of research20,22 recently being coupled with metabolic events through mitochondrial activity.4,9 Calcium events and proton flux have also been studied in rapidly growing polarized structures.2,3,5,7

Developmental problems focusing on the role of ion and molecular flux have also taken advantage of the advanced electrochemical approaches available through our self-referencing core activities. This has included observations on the movement of ions of calcium, potassium and hydrogen, as well as oxygen and ascorbate transport. A particularly interesting series of papers defined the two-pore potassium channel as a root player in early mammalian embryonic apoptosis (programmed cell death), an important component of controlled development. 8,12

Unlike many of the other thematic areas of study within the BRC, development still takes advantage of several non-mammalian model systems such as sea urchins, tunicates and amphibians. As these models are readily available at the MBL, and the integrated technologies available are at an ideal state to focus on questions of development and polarity, the BRC hosts a focused module in this area, coordinated by Professor K. Robinson of Purdue. Our current emphasis is on the underlying mechanisms behind left/right asymmetry.

Related projects at the BRC

• Membrane voltage in spinal cord/muscle regeneration >>
• Polarized ion transport during tip growth & directed cell motility >>
• Role of ion fluxes during regeneration >>
• Role of ion fluxes during patterning and embryogenesis >>
• Effect of hyperglycemia on living embryos >>
• Development & maintenance of the neuromuscular junction >>
• Electrical and ionic controls of developmental polarity >>
• Cell division & related motility >>

Related BRC publications

1) Li, R., Chase, M., Jung, S.-K., Smith, P.J.S., and Loeken, M.R. 2005. Hypoxic stress in diabetic pregnancy contributes to impaired embryo gene expression and defective development by inducing oxidative stress. American Journal of Physiology, Endocrinology and Metabolism, 289(4):E591-9.

2) Lew, R.R., Levina, N.N. 2004. Oxygen flux magnitude and location along growing hyphae of Neurospora crassa. FEMS Microbiology Letters, 233:125-130.
3) Messerli, M.A., Smith, P.J.S., Lewis, R.C. and Robinson, K.R. 2004. Chloride fluxes in lily pollen tubes: a critical reevaluation. Plant Journal, 40:799-812.
4) Dumollard, R., Hammar, K., Porterfield, M., Smith, P.J.S., Cibert, C., Rouviere, C. and Sardet, C. 2003. Mitochondrial respiration and Ca(2+) waves are linked during fertilization and meiosis completion. Development, 130(4): 683-692.
5) Messerli, M.A. and Robinson, K.R. 2003. Ionic and osmotic disruptions of the lily pollen tube oscillator: testing proposed models. Planta, 217(1): 147-57.
6) Robinson, K.R., Messerli, M.A. 2003. Left/right, up/down: the role of endogenous electrical fields as directional signals in development, repair and invasion. Bioessays, 25:759-766.
7) Robinson, K.R., and Messerli, M.A. 2002. Pulsating ion fluxes and growth at the pollen tube tip. Science's STKE, 2002(162): PE51.
8) Trimarchi, J.R., Liu, L., Smith, P.J.S. and Keefe, D.L. 2002. Apoptosis recruits two-pore domain potassium channels used for homeostatic volume regulation. American Journal of Physiology. Cell Physiology. 282: C588-C594.
9) Liu, L., Hammar, K., Smith, P.J.S., Inoue, S., Keefe, D. 2001. Mitochondrial modulation of calcium signaling at the initiation of development. Cell Calcium, 30(6): 423-433.
10) Danuser, G. and Oldenbourg, R. 2000. Probing f-actin flow by tracking shape fluctuations of radial bundles in Lamellipoda of motile cells. Biophysics Journal, 79: 191-201.
11) Oldenbourg, R., Katoh, K. and Danuser, G. 2000. Mechanism of lateral movement of filopodia and radial actin bundles across neuronal growth cones. Biophysical Journal, 78: 1176- 1182.
12) Trimarchi, J.R., Liu, L., Smith, P.J.S. and Keefe, D.L. 2000. Non-invasive measurement of potassium efflux as an early indicator of cell death in mouse embryos. Biology of Reprodution, 63: 851-857.

13) Trimarchi, J.R., Liu, L., Porterfield, D.M., Smith, P.J.S. and Keefe, D.L. 2000. A non-invasive method for measuring pre-implantation embryo physiology. Zygote, 8: 15-24.

14) Trimarchi, J.R., Liu, L., Porterfield, D.M., Smith, P.J.S. and Keefe, D.L. 2000. Oxidative phosphorylation-dependent and -independent oxygen consumption by individual preimplantation mouse embryos. Biology of Reproduction, 62: 1866-1874.
15) Katoh, K., Hammar, K., Smith, P.J.S. and Oldenbourg, R. 1999. Birefringence imaging directly reveals architectural dynamics of filamentous actin in living growth cones. Molecular Biology of the Cell, 10: 197-210.
16) Messerli, M.A., Danuser, G. and Robinson, K.R. 1999. Pulsatile influxes of H+, K+ and Ca++ lag growth pulses of Lilium longiflorum pollen tubes. Journal of Cell Science, 112: 1497-1509.
17) Pepperell, J.R., Kommineni, K., Buradagunta, S., Smith, P.J.S. and Keefe, D.L. 1999. Transmembrane regulation of intracellular calcium by a plasma membrane Sodium/Calcium exchanger in mouse oocytes. Biology of Reproduction, 60: 1137-1143.
18) Hill, J. L., Hammar, K., Smith, P. J. S. and Gross, D. 1999. Stage-dependent effects of epidermal growth factor on Ca2+ efflux in mouse oocytes. Molecular Reproduction and Development, 53: 244-253.
19) Katoh, K., Hammar, K., Smith, P.J.S. and Oldenbourg, R. 1999. Arrangement of radial actin bundles in the growth cone of Aplysia bag cell neurons shows a short history of filopodial behavior. Proceedings of the National Academy of Sciences, USA 96: 7928-7931.
20) Jaffe, L.F. 1999. Organization of early development by calcium patterns. BioEssays, 21: 657-667.
21) Lew, R.R. 1999. Comparative analysis of Ca2+ and H+ flux magnitude and location along growing hyphae of Saprolegnia ferax and Neurospora crassa. European Journal of Cell Biology, 78: 892-902.
22) Jaffe, L.F. and Creton, R. 1998. On the conservation of calcium wave speeds. Cell Calcium, 24(1): 1-8 (a review).
23) Porterfield, D.M., Trimarchi, J.R., Keefe, D.L. and Smith, P.J.S. 1998. Characterization of oxygen and calcium fluxes from early mouse embryos and oocytes. Biological Bulletin, 195: 208-209.
24) Katoh, K., Langford, G., Hammar, K., Smith, P.J.S. and Oldenbourg, R. 1997. Observation of actin bundles in neural growth cone with the Oldenbourg Pol-Scope. Biological Bulletin, 193: 219-220.
25) Pierson, E.S., Miller, D.D., Callaham, D.A., van Aken, J., Hackett, G. and Hepler, P.K. 1996. Tip-localized calcium entry fluctuates during pollen tube growth. Developmental Biology, 174: 160-173.
26) Dube, F. and Eckberg, W.R. 1996. Intracellular pH measurements during fertilization of surf clam (Spisula solidissima) oocytes. Biological Bulletin, 191: 279-280.
27) Eckberg, W.R. and Dube, F. 1996. Effects of altering pHi and pHo on the activation of Chaetopterus eggs. Biological Bulletin,191: 280-281.

Click on article titles for links to PubMed abstracts and PDF files (underlined when available).

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