Antony Galione

Last updated

Antony Galione

Professor Antony Galione FMedSci FRS (cropped).jpg
Galione in 2016
Born (1963-09-13) 13 September 1963 (age 59) [1]
Chelmsford, England
Education Felsted School
Alma mater Trinity College, Cambridge
Spouse
Angela Clayton
(m. 1992)
[1]
AwardsNovartis Prize (2001) [2]
Scientific career
Fields
Institutions
Thesis Oscillations in intracellular calcium in the blowfly salivary gland  (1989)
Doctoral advisor Michael Berridge [4]
Website pharm.ox.ac.uk/team/antony-galione

Antony Giuseppe Galione FRS FMedSci [5] (born 13 September 1963) [1] is a British pharmacologist. He is a professor and Wellcome Trust senior investigator in the Department of Pharmacology at the University of Oxford. [4]

Contents

Early life and education

Antony Giuseppe Galione was born on 13 September 1963 in Chelmsford, England, to Angelo and Margaret Galione. [1] He was educated at Felsted School [1] in Essex and Trinity College, Cambridge, where he was awarded a Bachelor of Arts degree in Natural Sciences (Pharmacology) in 1985 [4] followed by a PhD in 1989 for research on calcium signalling in the salivary gland of the blowfly, supervised by Michael Berridge. [6] [7]

Research and career

Galione's research investigates calcium signalling. [3] HC Lee established the concept of multiple calcium mobilising messengers which link cell surface stimuli to release of internal calcium stores, while Zhu, Evans and co-workers identified their target two-pore channels (TPCs) and organelles. [8] This has enhanced our understanding of how calcium as a ubiquitous cellular regulator may control a myriad of cellular processes with precision. [5]

Galione established that cyclic ADP-ribose regulates calcium-induced calcium release and globalisation of calcium signals, [9] and that Nicotinic acid adenine dinucleotide phosphate (NAADP) is a ubiquitous trigger for initiating and co-ordinating calcium signals, often involving communication between organelles at contact sites. [5]

By developing novel pharmacological, molecular and physiological approaches, he has demonstrated that these messengers and their targets regulate many fundamental pathophysiological cellular processes as diverse as Ebola virus disease infection, fertilisation and embryology, cardiac contractility, T cell activation and neuronal excitability. The discovery of lysosomes as calcium stores mobilised by NAADP has identified an entirely new signalling role for these organelles in health and disease. [5] [10]

Galione served as head of the Department of Pharmacology at the University of Oxford from 2006 until 2015. [11]

Awards and honours

Galione was elected a Fellow of the Academy of Medical Sciences (FMedSci) in 2010 [5] a Fellow of the Royal Society (FRS) in 2016. [5] He was awarded the Novartis Prize from the British Pharmacological Society in 2001. [2]

Related Research Articles

<span class="mw-page-title-main">Nucleotide</span> Biological molecules that form the building blocks of nucleic acids

Nucleotides are organic molecules composed of a nitrogenous base, a pentose sugar and a phosphate. They serve as monomeric units of the nucleic acid polymers – deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), both of which are essential biomolecules within all life-forms on Earth. Nucleotides are obtained in the diet and are also synthesized from common nutrients by the liver.

<span class="mw-page-title-main">Nicotinamide adenine dinucleotide</span> Chemical compound which is reduced and oxidized

Nicotinamide adenine dinucleotide (NAD) is a coenzyme central to metabolism. Found in all living cells, NAD is called a dinucleotide because it consists of two nucleotides joined through their phosphate groups. One nucleotide contains an adenine nucleobase and the other, nicotinamide. NAD exists in two forms: an oxidized and reduced form, abbreviated as NAD+ and NADH (H for hydrogen), respectively.

Dale Sanders, FRS was Director of the John Innes Centre, an institute for research in plant sciences and microbiology in Norwich, England.

Ryanodine receptors form a class of intracellular calcium channels in various forms of excitable animal tissue like muscles and neurons. There are three major isoforms of the ryanodine receptor, which are found in different tissues and participate in different signaling pathways involving calcium release from intracellular organelles. The RYR2 ryanodine receptor isoform is the major cellular mediator of calcium-induced calcium release (CICR) in animal cells.

<span class="mw-page-title-main">Calcium signaling</span> Intracellular communication process

Calcium signaling is the use of calcium ions (Ca2+) to communicate and drive intracellular processes often as a step in signal transduction. Ca2+ is important for cellular signalling, for once it enters the cytosol of the cytoplasm it exerts allosteric regulatory effects on many enzymes and proteins. Ca2+ can act in signal transduction resulting from activation of ion channels or as a second messenger caused by indirect signal transduction pathways such as G protein-coupled receptors.

<span class="mw-page-title-main">CD38</span> Protein-coding gene in the species Homo sapiens

CD38 (cluster of differentiation 38), also known as cyclic ADP ribose hydrolase is a glycoprotein found on the surface of many immune cells (white blood cells), including CD4+, CD8+, B lymphocytes and natural killer cells. CD38 also functions in cell adhesion, signal transduction and calcium signaling.

<span class="mw-page-title-main">Diphtheria toxin</span> Exotoxin

Diphtheria toxin is an exotoxin secreted mainly by Corynebacterium diphtheriae but also by Corynebacterium ulcerans and Corynebacterium pseudotuberculosis. the pathogenic bacterium that causes diphtheria. The toxin gene is encoded by a prophage called corynephage β. The toxin causes the disease in humans by gaining entry into the cell cytoplasm and inhibiting protein synthesis.

Sir Michael John Berridge was a British physiologist and biochemist.

Two-pore channels (TPCs) are eukaryotic intracellular voltage-gated and ligand gated cation selective ion channels. There are two known paralogs in the human genome, TPC1s and TPC2s. In humans, TPC1s are sodium selective and TPC2s conduct sodium ions, calcium ions and possibly hydrogen ions. Plant TPC1s are non-selective channels. Expression of TPCs are found in both plant vacuoles and animal acidic organelles. These organelles consist of endosomes and lysosomes. TPCs are formed from two transmembrane non-equivalent tandem Shaker-like, pore-forming subunits, dimerized to form quasi-tetramers. Quasi-tetramers appear very similar to tetramers, but are not quite the same. Some key roles of TPCs include calcium dependent responses in muscle contraction(s), hormone secretion, fertilization, and differentiation. Disorders linked to TPCs include membrane trafficking, Parkinson's disease, Ebola, and fatty liver.

<span class="mw-page-title-main">Ruthenium red</span> Chemical compound

The inorganic dye ammoniated ruthenium oxychloride, also known as ruthenium red, is used in histology to stain aldehyde fixed mucopolysaccharides.

<span class="mw-page-title-main">Cyclic ADP-ribose</span> Chemical compound

Cyclic ADP Ribose, frequently abbreviated as cADPR, is a cyclic adenine nucleotide (like cAMP) with two phosphate groups present on 5' OH of the adenosine (like ADP), further connected to another ribose at the 5' position, which, in turn, closes the cycle by glycosidic bonding to the nitrogen 1 (N1) of the same adenine base (whose position N9 has the glycosidic bond to the other ribose). The N1-glycosidic bond to adenine is what distinguishes cADPR from ADP-ribose (ADPR), the non-cyclic analog. cADPR is produced from nicotinamide adenine dinucleotide (NAD+) by ADP-ribosyl cyclases (EC 3.2.2.5) as part of a second messenger system.

<span class="mw-page-title-main">Nicotinic acid adenine dinucleotide phosphate</span> Chemical compound

Nicotinic acid adenine dinucleotide phosphate, (NAADP), is a Ca2+-mobilizing second messenger synthesised in response to extracellular stimuli. Like its mechanistic cousins, IP3 and cyclic adenosine diphosphoribose (Cyclic ADP-ribose), NAADP binds to and opens Ca2+ channels on intracellular organelles, thereby increasing the intracellular Ca2+ concentration which, in turn, modulates sundry cellular processes (see Calcium signalling). Structurally, it is a dinucleotide that only differs from the house-keeping enzyme cofactor, NADP by a hydroxyl group (replacing the nicotinamide amino group) and yet this minor modification converts it into the most potent Ca2+-mobilizing second messenger yet described. NAADP acts across phyla from plants to humans.

<span class="mw-page-title-main">Adenosine diphosphate ribose</span> Chemical compound

Adenosine diphosphate ribose (ADPR) is an ester molecule formed into chains by the enzyme poly ADP ribose polymerase. ADPR is created from cyclic ADP-ribose (cADPR) by the CD38 enzyme using nicotinamide adenine dinucleotide (NAD+) as a cofactor.

In enzymology, a NAD+ glycohydrolase (EC 3.2.2.5) is an enzyme that catalyzes the chemical reaction

<span class="mw-page-title-main">TPCN1</span> Protein-coding gene in the species Homo sapiens

Two pore segment channel 1 (TPC1) is a human protein encoded by the TPCN1 gene. The protein encoded by this gene is an ion channel. In contrast to other calcium and sodium channels which have four homologous domains, each containing 6 transmembrane segments, TPCN1 only contains two domains.

<span class="mw-page-title-main">TPCN2</span> Protein-coding gene in the species Homo sapiens

Two pore segment channel 2 (TPC2) is a protein which in humans is encoded by the TPCN2 gene. TPC2 is an ion channel, however, in contrast to other calcium and sodium channels which have four homologous domains, each containing 6 transmembrane segments, TPCN1 only contains two domain.

<span class="mw-page-title-main">Annette Dolphin</span> Professor of Pharmacology

Annette Catherine Dolphin is a Professor of Pharmacology in the Department of Neuroscience, Physiology and Pharmacology at University College London (UCL).

<span class="mw-page-title-main">Barry V. L. Potter</span> British biochemist

Barry Victor Lloyd Potter MAE FMedSci is a British chemist, who is Professor of Medicinal & Biological Chemistry at the University of Oxford, Wellcome Trust Senior Investigator and a Fellow of University College, Oxford.

Anant B. Parekh is professor of Physiology at the University of Oxford and a Fellow of Merton College, Oxford.

<span class="mw-page-title-main">NED-19</span> Chemical compound

Trans-NED-19 is a drug which acts as a potent and selective antagonist of the endogenous calcium channel opener nicotinic acid adenine dinucleotide phosphate (NAADP), thereby reducing the normal NAADP-mediated calcium flux without blocking calcium channels directly. It is used in research into the functions of NAADP signalling inside many different cell types.

References

  1. 1 2 3 4 5 "Galione, Prof. Antony Giuseppe" . Who's Who . A & C Black. 2021. doi:10.1093/ww/9780199540884.013.U246727.(Subscription or UK public library membership required.)
  2. 1 2 "Novartis Prize". bps.ac.uk. British Pharmacological Society. Archived from the original on 4 August 2017. Retrieved 3 August 2017.
  3. 1 2 Antony Galione publications indexed by Google Scholar
  4. 1 2 3 "Professor Antony Galione FMedSci FRS". Oxford: University of Oxford. Archived from the original on 23 March 2016.
  5. 1 2 3 4 5 6 Anon (2016). "Professor Antony Galione FMedSci FRS". London: Royal Society. Archived from the original on 29 April 2016. One or more of the preceding sentences incorporates text from the royalsociety.org website where:
    "All text published under the heading 'Biography' on Fellow profile pages is available under Creative Commons Attribution 4.0 International License." -- "Royal Society Terms, conditions and policies". Archived from the original on 25 September 2015. Retrieved 9 March 2016.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  6. Galione, Antony Giuseppe (1989). Oscillations in intracellular calcium in the blowfly salivary gland (PhD thesis). University of Cambridge. OCLC   53486297.
  7. Berridge MJ, Galione A (1988). "Cytosolic calcium oscillators". The FASEB Journal . 2 (15): 3074–82. doi:10.1096/fasebj.2.15.2847949. PMID   2847949. S2CID   21782086.
  8. Calcraft, Peter J.; Ruas, Margarida; Pan, Zui; Cheng, Xiaotong; Arredouani, Abdelilah; Hao, Xuemei; Tang, Jisen; Rietdorf, Katja; Teboul, Lydia; Chuang, Kai-Ting; Lin, Peihui; Xiao, Rui; Wang, Chunbo; Zhu, Yingmin; Lin, Yakang; Wyatt, Christopher N.; Parrington, John; Ma, Jianjie; Evans, A. Mark; Galione, Antony; Zhu, Michael X. (2009). "NAADP mobilizes calcium from acidic organelles through two-pore channels". Nature . 459 (7246): 596–600. Bibcode:2009Natur.459..596C. doi:10.1038/nature08030. PMC   2761823 . PMID   19387438.
  9. Galione, A.; Lee, H.; Busa, W. (1991). "Ca(2+)-induced Ca2+ release in sea urchin egg homogenates: modulation by cyclic ADP-ribose". Science . 253 (5024): 1143–1146. Bibcode:1991Sci...253.1143G. doi:10.1126/science.1909457. PMID   1909457. S2CID   43565315.
  10. Arredouani A, Ruas M, Collins SC, Parkesh R, Clough F, Pillinger T, et al. (2015). "Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) and Endolysosomal Two-pore Channels Modulate Membrane Excitability and Stimulus-Secretion Coupling in Mouse Pancreatic β Cells". Journal of Biological Chemistry . 290 (35): 21376–92. doi: 10.1074/jbc.M115.671248 . PMC   4571866 . PMID   26152717. Open Access logo PLoS transparent.svg
  11. "Antony Galione". University of Oxford. Archived from the original on 4 August 2017. Retrieved 3 August 2017.