John Gurdon

نویسنده

  • John Gurdon
چکیده

significant hurdles that are only just beginning to be overcome. Complex cell behaviors, such as migration, result from coordinated activity of several individual component processes. While considerable progress has been made in identifying molecules related to migration and elucidating the mechanisms by which they function in a component process, understanding the integration of these various component processes presents a major challenge. Fortunately, technologies are emerging that allow us to study the spatial and temporal regulation that generates the coordination of these processes. These include biosensors that allow spatially resolved assays of signaling events in real time in living cells and photomanipulative techniques that allow local perturbations of function via photoactivation or inactivation to complement the observations made using biosensors. It is now clear that migration in vivo differs from that studied in vitro; this may reflect different signaling mechanisms or cellular mechanics. The development of three-dimensional systems that allow imaging of cellular and molecular dynamics is helping to reveal mechanisms underlying migration in physiological environments. Finally, the signals that initiate, guide, and stop migration are not well understood, especially in the context of the component processes of migration and their regulation. Cell Migration as a Discipline Until recently, research in cell migration was split into a number of subdisciplines that did not interact as an integrated research area. Over the past few years, cell migration has emerged as its own discipline. Recently, an NIH-sponsored Cell Migration Consortium was formed (www.cellmigration.org) with the aim of promoting migration research by addressing some major barriers to progress in the field. These include a census of the migration proteome, the structure of the supramolecular complexes that drive migration, development of novel signaling reagents that report spatially resolved signals in living cells, development of mathematical models of migration, development of novel imaging techniques, development of new biomaterials, and the production of knockout, knockin and knockdown mice and cell lines. Other Consortium activities include promoting interdisciplinary collaboration and organizing information in the field through a web-based cell migration knowledge database. Cellular motility driven by assembly and disassembly of actin filaments. (2000). Leukocytes navigate by compass: roles of PI3Kgamma and its lipid products. (2001). Human brain malformations and their lessons for neuronal migration. changed from classics to zoology. During graduate work under Michael Fischberg at Oxford, he was the first to obtain a normal adult animal by somatic cell nuclear transfer. He then spent a year on …

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منابع مشابه

"Developmental Capacity of Nuclei Transplanted from Keratinized Skin Cells of Adult Frogs" (1975), by John Gurdon, Ronald Laskey, and O. Raymond Reeves

In 1975 John Gurdon [4], Ronald Laskey [5], and O. Raymond Reeves [6] published ?Developmental Capacity of Nuclei Transplanted from Keratinized Skin Cells of Adult Frogs,? in the Journal of Embryology and Experimental Morphology. Their article was the capstone of a series of experiments performed by Gurdon during his time at Oxford and Cambridge, using the frog [7] species Xenopus laevis [8]. G...

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"The Developmental Capacity of Nuclei Taken from Intestinal Epithelium Cells of Feeding Tadpoles" (1962), by John B. Gurdon

In 1962 researcher John Bertrand Gurdon at the University of Oxford [3] in Oxford, England conducted a series of experiments on the developmental capacity of nuclei taken from intestinal epithelium [4] cells of feeding tadpoles. In the experiments, Gurdon conducted nuclear transplantation, or cloning [5], of differentiated cells, or cells that have already specialized to become one cell type or...

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Sir John Gurdon: father of nuclear reprogramming.

Sir John Gurdon founded the field of nuclear reprogramming. His work set the stage for the ever burgeoning area of stem cell biology and regenerative medicine. Here I provide personal reflections on times I shared with John Gurdon and professional reflections of the impact of his ground-breaking research on my own development as a scientist and on the field in general. His paradigm-shifting exp...

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An interview with John Gurdon.

John Gurdon is a Distinguished Group Leader in the Wellcome Trust/Cancer Research UK Gurdon Institute and Professor Emeritus in the Department of Zoology at the University of Cambridge. In 2012, he was awarded the Nobel Prize in Physiology or Medicine jointly with Shinya Yamanaka for work on the reprogramming of mature cells to pluripotency, and his lab continues to investigate the molecular me...

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The egg and the nucleus: a battle for supremacy (Nobel Lecture).

Sir John Gurdon and Professor Shinya Yamanaka were the recipients of the 2012 Nobel Prize for Physiology or Medicine. This Spotlight article is a commentary on the early nuclear transplant work in Xenopus, which was very important for the Nobel award in 2012, and the influence of this work on the reprogramming field.

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Epigenetic memory and parliamentary privilege combine to evoke discussions on inheritance

Understanding the basis of epigenetic memory is a fast-moving challenge in modern biology. At a recent Company of Biologists Workshop held at Steyning’s historic Wiston House, thirty researchers led by John Gurdon interrogated three central questions: how are cell type-specific programs generated, what mechanisms duplicate this programmatic information as cells divide, and how does epigenetics ...

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عنوان ژورنال:
  • Current Biology

دوره 13  شماره 

صفحات  -

تاریخ انتشار 2003