Christopher Coates

Dr. Christopher Coates

Department of Biosciences, College of Science, Swansea University, Swansea SA2 8PP, Wales UK
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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2016
Verified
Book Chapter
Closed access
TBTariq Butt
Tariq Butt
CCChristopher Coates
Christopher Coates
Ivan DubovskiyIvan Dubovskiy
Ivan Dubovskiy
NRN.A. Ratcliffe
N.A. Ratcliffe

1 July 2014 in Developmental & Comparative Immunology
Verified
Journal Article
Closed access
CCChristopher Coates
Christopher Coates
JNJacqueline Nairn
Jacqueline Nairn

12 August 2016 in Cellular and Molecular Life Sciences
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Journal Article
Open access
PDF file
CCChristopher Coates
Christopher Coates
HDHeinz Decker
Heinz Decker
It is now well documented that peptides with enhanced or alternative functionality (termed cryptides) can be liberated from larger, and sometimes inactive, proteins. A primary example of this phenomenon is the oxygen-transport protein hemoglobin. Aside from respiration, hemoglobin and hemoglobin-derived peptides have been associated with immune modulation, hematopoiesis, signal transduction and microbicidal activities in metazoans. Likewise, the functional equivalents to hemoglobin in invertebrates, namely hemocyanin and hemerythrin, act as potent immune effectors under certain physiological conditions. The purpose of this review is to evaluate the true extent of oxygen-transport protein dynamics in innate immunity, and to impress upon the reader the multi-functionality of these ancient proteins on the basis of their structures. In this context, erythrocyte–pathogen antibiosis and the immune competences of various erythroid cells are compared across diverse taxa.

13 June 2017 in Pigment Cell & Melanoma Research
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Journal Article
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MWMiranda M. A. Whitten
Miranda M. A. Whitten
CCChristopher Coates
Christopher Coates

7 December 2017 in Journal of Innate Immunity
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Journal Article
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CCChristopher Coates
Christopher Coates
CMClaire McCulloch
Claire McCulloch
JBJoshua Betts
Joshua Betts
TWTim Whalley
Tim Whalley
Cellular immune defences in sea urchins are shared amongst the coelomocytes - a heterogeneous population of cells residing in the coelomic fluid (blood equivalent) and tissues. The most iconic coelomocyte morphotype is the red spherule cell (or amebocyte), so named due to the abundance of cytoplasmic vesicles containing the naphthoquinone pigment echinochrome A. Despite their identification over a century ago, and evidence of antiseptic properties, little progress has been made in characterising the immunocompetence of these cells. Upon exposure of red spherule cells from sea urchins, i.e., Paracentrotus lividus and Psammechinus miliaris, to microbial ligands, intact microbes, and damage signals, we observed cellular degranulation and increased detection of cell-free echinochrome in the coelomic fluid ex vivo. Treatment of the cells with ionomycin, a calcium-specific ionophore, confirmed that an increase in intracellular levels of Ca2+ is a trigger of echinochrome release. Incubating Gram-positive/negative bacteria as well as yeast with lysates of red spherule cells led to significant reductions in colony-forming units. Such antimicrobial properties were counteracted by the addition of ferric iron (Fe3+), suggesting that echinochrome acts as a primitive iron chelator in echinoid biological defences.

1 February 2010 in Microbes and Infection
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Journal Article
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PMPeter Mowlds
Peter Mowlds
CCChristopher Coates
Christopher Coates
JRJulie Renwick
Julie Renwick
KKKevin Kavanagh
Kevin Kavanagh