Russell Foster | |
---|---|
Born | |
Nationality | British |
Alma mater | University of Bristol |
Awards | Honma Prize (Japan), David G. Cogan Award (USA), Zoological Society Scientific and Edridge-Green Medals (UK) |
Scientific career | |
Fields | Neuroscience |
Institutions | University of Oxford |
Thesis | An investigation of the extraretinal photoreceptors mediating photoperiodic induction in the Japanese quail (Coturnix coturnix japonica) (1978) |
Academic advisors | Brian Follett |
Website | www |
Russell Grant Foster, CBE, FRS FMedSci (born 1959) [1] [2] is a British professor of circadian neuroscience, the Director of the Nuffield Laboratory of Ophthalmology and the Head of the Sleep and Circadian Neuroscience Institute (SCNi). [3] [4] He is also a Nicholas Kurti Senior Fellow at Brasenose College [5] at the University of Oxford. [6] Foster and his group are credited with key contributions to the discovery of the non-rod, non-cone, photosensitive retinal ganglion cells (pRGCs) in the mammalian retina which provide input to the circadian rhythm system. He has written and co-authored over a hundred scientific publications. [6]
Since 2018 he has been Editor-in-Chief of the Royal Society journal Interface Focus .
Foster attended Heron Wood School in his native Aldershot and studied at the University of Bristol and graduated with a Bachelor of Science (BSc) in Zoology in 1980. He also carried out postgraduate studies at the University of Bristol under the supervision of Brian Follett, and was awarded a PhD in 1984 for his thesis entitled An investigation of the extraretinal photoreceptors mediating photoperiodic induction in the Japanese quail (Coturnix coturnix japonica). [7] [8]
From 1988 to 1995 Foster was a member of the National Science Foundation Center for Biological Rhythms at the University of Virginia, where he worked closely with Michael Menaker. [4] In 1995, he returned to UK and started his own lab at Imperial College, where he became Chair of Molecular Neuroscience within the Faculty of Medicine. He later transferred his laboratory to the University of Oxford to engage in more translational research. [9]
While at the University of Virginia, Foster and Menaker performed experiments where the suprachiasmatic nucleus (SCN) was tested by neural transplantation of donor's SCN to a recipient with an ablated SCN. In the experiment, the donor was a mutant strain of hamster with a shortened circadian period. The recipient was a wild-type hamster. Transplantation was done the other way around as well, with wild-type hamster as the donor and mutant strain hamster as the recipient. After the transplantation, the formerly wild-type hamster displayed a shortened period which resembled the mutant, and the mutant-strain hamster showed normal period. The SCN restored rhythm to arrhythmic recipients, which afterwards always exhibited the circadian period of the donor. This result led to the conclusion that the SCN is sufficient and necessary for mammalian circadian rhythms. [10]
In 1991, Foster and his colleagues provided evidence that rods and cones are not necessary for entrainment of an animal to light. [11] In this experiment, Foster gave light pulses to retinally degenerative mice. These mice were homozygous for the rd allele and were shown to have no rods in their retina. Only a few cones were found to remain in the retina. To study the effects of light entrainment, magnitude of phase shift of locomotor activity was measured. The results showed that both mice with normal retina and mice with degenerate retina showed similar entrainment patterns. Foster hypothesized that circadian photoreception occurs with a small number of cones without an outer layer or that an unrecognised class of photoreceptive cells are present.
In 1999, Foster studied light entrainment on mice without cones or both rods and cones. [12] Mice without cones or without both photoreceptive cells (rd/rd cl allele) still entrained to light. Meanwhile, mice with eyes removed could not entrain to light. Foster concluded that rods and cones are unnecessary for entrainment to light, and that the murine eye contains additional photoreceptive cell types. Later studies showed that melanopsin expressing photoreceptive retinal ganglion cells (pGRCs) were accountable for non-rod, non-cone entrainment to light. [13] [14]
He is the co-author with writer and broadcaster Leon Kreitzman of two popular science books on circadian rhythms, Rhythms of Life: The Biological Clocks that Control the Daily Lives of Every Living Thing [15] [16] and Seasons of Life: The Biological Rhythms That Enable Living Things to Thrive and Survive. [17] He has also co-written a book titled Sleep: a Very Short Introduction. [18] He wrote Life Time : The New Science of the Body Clock, and How It Can Revolutionize Your Sleep and Health. [19]
Foster was elected a fellow of the Royal Society in 2008. [3]
Foster was appointed Commander of the Order of the British Empire (CBE) in the 2015 New Year Honours for services to science. [20] [21]
Russell Foster was awarded with The Daylight Award 2020 in the category Daylight Research, for his clinical studies in humans addressing important questions regarding light.
Foster has received recognition from around the world for his discovery of pRGCs:
Chronobiology is a field of biology that examines timing processes, including periodic (cyclic) phenomena in living organisms, such as their adaptation to solar- and lunar-related rhythms. These cycles are known as biological rhythms. Chronobiology comes from the ancient Greek χρόνος, and biology, which pertains to the study, or science, of life. The related terms chronomics and chronome have been used in some cases to describe either the molecular mechanisms involved in chronobiological phenomena or the more quantitative aspects of chronobiology, particularly where comparison of cycles between organisms is required.
A photoreceptor cell is a specialized type of neuroepithelial cell found in the retina that is capable of visual phototransduction. The great biological importance of photoreceptors is that they convert light into signals that can stimulate biological processes. To be more specific, photoreceptor proteins in the cell absorb photons, triggering a change in the cell's membrane potential.
The suprachiasmatic nucleus or nuclei (SCN) is a small region of the brain in the hypothalamus, situated directly above the optic chiasm. It is responsible for regulating sleep cycles in animals. Reception of light inputs from photosensitive retinal ganglion cells allow it to coordinate the subordinate cellular clocks of the body and entrain to the environment. The neuronal and hormonal activities it generates regulate many different body functions in an approximately 24-hour cycle.
Melanopsin is a type of photopigment belonging to a larger family of light-sensitive retinal proteins called opsins and encoded by the gene Opn4. In the mammalian retina, there are two additional categories of opsins, both involved in the formation of visual images: rhodopsin and photopsin in the rod and cone photoreceptor cells, respectively.
Intrinsically photosensitive retinal ganglion cells (ipRGCs), also called photosensitive retinal ganglion cells (pRGC), or melanopsin-containing retinal ganglion cells (mRGCs), are a type of neuron in the retina of the mammalian eye. The presence of an additional photoreceptor was first suspected in 1927 when mice lacking rods and cones still responded to changing light levels through pupil constriction; this suggested that rods and cones are not the only light-sensitive tissue. However, it was unclear whether this light sensitivity arose from an additional retinal photoreceptor or elsewhere in the body. Recent research has shown that these retinal ganglion cells, unlike other retinal ganglion cells, are intrinsically photosensitive due to the presence of melanopsin, a light-sensitive protein. Therefore, they constitute a third class of photoreceptors, in addition to rod and cone cells.
In neuroanatomy, the retinohypothalamic tract (RHT) is a photic neural input pathway involved in the circadian rhythms of mammals. The origin of the retinohypothalamic tract is the intrinsically photosensitive retinal ganglion cells (ipRGC), which contain the photopigment melanopsin. The axons of the ipRGCs belonging to the retinohypothalamic tract project directly, monosynaptically, to the suprachiasmatic nuclei (SCN) via the optic nerve and the optic chiasm. The suprachiasmatic nuclei receive and interpret information on environmental light, dark and day length, important in the entrainment of the "body clock". They can coordinate peripheral "clocks" and direct the pineal gland to secrete the hormone melatonin.
Ignacio Provencio is an American neuroscientist and the discoverer of melanopsin, an opsin found in specialized photosensitive ganglion cells of the mammalian retina. Provencio served as the program committee chair of the Society for Research on Biological Rhythms from 2008 to 2010.
Light effects on circadian rhythm are the response of circadian rhythms to light.
Joseph S. Takahashi is a Japanese American neurobiologist and geneticist. Takahashi is a professor at University of Texas Southwestern Medical Center as well as an investigator at the Howard Hughes Medical Institute. Takahashi's research group discovered the genetic basis for the mammalian circadian clock in 1994 and identified the Clock gene in 1997. Takahashi was elected to the National Academy of Sciences in 2003.
King-Wai Yau is a Chinese-born American neuroscientist and Professor of Neuroscience at Johns Hopkins University School of Medicine in Baltimore, Maryland.
Michael Menaker, was an American chronobiologist who was Commonwealth Professor of Biology at University of Virginia. His research focused on circadian rhythmicity of vertebrates, including contributing to an understanding of light input pathways on extra-retinal photoreceptors of non-mammalian vertebrates, discovering a mammalian mutation for circadian rhythmicity, and locating a circadian oscillator in the pineal gland of bird. He wrote almost 200 scientific publications.
Arnold Eskin was a professor of chronobiology at the University of Houston in Houston, Texas. He attended Vanderbilt University, where he received a degree in physics. He later attended University of Texas at Austin, where he received his Ph.D. in zoology in 1969. He is recognized in the term Eskinogram, and has been a leader in the discovery of mechanisms underlying entrainment of circadian clocks.
Douglas G. McMahon is a professor of Biological Sciences and Pharmacology at Vanderbilt University. McMahon has contributed several important discoveries to the field of chronobiology and vision. His research focuses on connecting the anatomical location in the brain to specific behaviors. As a graduate student under Gene Block, McMahon identified that the basal retinal neurons (BRNs) of the molluscan eye exhibited circadian rhythms in spike frequency and membrane potential, indicating they are the clock neurons. He became the 1986 winner of the Society for Neuroscience's Donald B. Lindsley Prize in Behavioral Neuroscience for his work. Later, he moved on to investigate visual, circadian, and serotonergic mechanisms of neuroplasticity. In addition, he helped find that constant light can desynchronize the circadian cells in the suprachiasmatic nucleus (SCN). He has always been interested in the underlying causes of behavior and examining the long term changes in behavior and physiology in the neurological modular system. McMahon helped identifying a retrograde neurotransmission system in the retina involving the melanopsin containing ganglion cells and the retinal dopaminergic amacrine neurons.
Robert Y. Moore is an American neurologist with interests in disorders of biological rhythms, movement disorders, and behavioral neurology. He is credited with discovering the function of the suprachiasmatic nucleus (SCN) as the circadian clock, as well as, describing its organization. He is also credited with establishing the role of the mammalian retinohypothalamic tract (RHT) as a photic entrainment pathway. Moore cin 2017 serves as a professor of neurology, with a secondary in psychiatry and neuroscience at the University of Pittsburgh, and as co-director of the National Parkinson Foundation Center of Excellence at the University of Pittsburgh.
Johanna H. Meijer is a Dutch scientist who has contributed to the field of chronobiology. She started a national wide program, involving eight Dutch universities to study the effects of clock disturbance on human health and biodiversity. Notably, Meijer is the 2016 recipient of the Aschoff and Honma Prize.
Elizabeth Maywood is an English researcher who studies circadian rhythms and sleep in mice. Her studies are focused on the suprachiasmatic nucleus (SCN), a small region of the brain that controls circadian rhythms.
Dr. Debra J. Skene is a chronobiologist with specific interest in the mammalian circadian rhythm and the consequences of disturbing the circadian system. She is also interested in finding their potential treatments for people who suffer from circadian misalignment. Skene and her team of researchers tackle these questions using animal models, clinical trials, and most recently, liquid chromatography-mass spectrometry. Most notably, Skene is credited for her evidence of a novel photopigment in humans, later discovered to be melanopsin. She was also involved in discovering links between human PER3 genotype and an extremely shifted sleep schedules categorized as extreme diurnal preference. Skene received her Bachelor of Pharmacy, Master of Science, and Ph.D. in South Africa.
In chronobiology, photoentrainment refers to the process by which an organism's biological clock, or circadian rhythm, synchronizes to daily cycles of light and dark in the environment. The mechanisms of photoentrainment differ from organism to organism. Photoentrainment plays a major role in maintaining proper timing of physiological processes and coordinating behavior within the natural environment. Studying organisms’ different photoentrainment mechanisms sheds light on how organisms may adapt to anthropogenic changes to the environment.
Russell Van Gelder is an American clinician-scientist and board-certified ophthalmologist; he has served as the chair of the University of Washington Medicine Department of Ophthalmology since 2008 and Editor-in-Chief of the journal Ophthalmology since 2022. He is known for his research on the mechanisms of uveitis, non-visual photoreception in the eye, and vision-restoration methods for retinal degenerative disease, as well as his leadership and advisory positions in various American ophthalmological and medical societies.
Martin R. Ralph is a circadian biologist who serves as a professor in the Psychology Department at the University of Toronto. His research primarily focuses on circadian rhythmicity in the fields of neuroscience, psychology, and endocrinology. His most notable work has been on the suprachiasmatic nucleus, now recognized as the central circadian pacemaker in mammals, but has also investigated circadian rhythms in the context of time, memory, and light.
{{cite book}}
: CS1 maint: multiple names: authors list (link){{cite book}}
: CS1 maint: multiple names: authors list (link)