William Joseph Schwartz | |
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Born | Philadelphia, US | March 28, 1950
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William Joseph Schwartz (born March 28, 1950) is an American neurologist and scientist who serves as Professor and Associate Chair for Research and Education in the neurology department at the University of Texas Dell Medical School. His work on the neurobiology of circadian timekeeping has focused on the mammalian suprachiasmatic nucleus. [1] Schwartz demonstrated that the suprachiasmatic nucleus is rhythmic in vivo using a 2-deoxyglucose radioactive marker for functional brain imaging. [2] As of 2014, he is editor of the Journal of Biological Rhythms . [3]
Schwartz was born on March 28, 1950, in Philadelphia, Pennsylvania. In 1959, he moved to southern California with his family. He began his undergraduate education at the University of Southern California in Los Angeles and, in 1971, finished his Bachelor of Science degree in biological sciences at the University of California, Irvine. [4] He completed his M.D. in 1974 and a medical internship from 1974 to 1975 both at the University of California, San Francisco. From 1975–1978, Schwartz did a research fellowship at the National Institute of Mental Health. [1] He finished his neurology residency training (1978–1981) at the University of California, San Francisco.
Following his residency training, Schwartz joined the faculties of Harvard Medical School and the Massachusetts General Hospital between 1981 and 1986. Schwartz then moved to the University of Massachusetts Medical School, where he held dual positions in the Neurology Department at the School of Medicine, and in the Neuroscience Department at the Graduate School of Biomedical Sciences. [1]
Schwartz has held visiting fellowships at several universities including but not limited to the Leiden University Medical Center (2005) in the Netherlands, Rijksuniversiteit Groningen (2008) also in the Netherlands, at the University of Auckland (2012) in New Zealand, and at Washington University in St. Louis (2016), in the United States.
As of 2017, Schwartz is the Associate Chair of Research and Education Neurology at the University of Texas at Austin Dell Medical School. [5]
Schwartz serves as the editor-in-chief of the Journal of Biological Rhythms [6] from 2014–present, and was previously elected as the Chair of the Gordon Research Conference on Chronobiology (1993) and President of the Society for Research on Biological Rhythms (2004–2006).
In 1977, Schwartz, along with Harold Gainer, Ph.D, [7] found that the glucose consumption in the rat suprachiasmatic nucleus is a function of time of day and environmental lighting conditions. [2]
Glucose consumption was studied via a technique using 14C-deoxyglucose (DG). DG is transported into the brain via the same mechanism which transports glucose, where it is then phosphorylated by hexokinase into 14C-deoxyglucose-6-phosphate(DG-6-P). The accumulation of DG-6-P reflects the rate of glucose consumption, and can be quantitatively measured using an autoradiograph. This method can be used to visualize activity in different regions of the brain. Schwartz's work with this method contributed to its early utilization and application, demonstrating that the method primarily measures energy demands of the synaptic, rather than the spiking, activities of neural tissue. This insight has been key to the interpretation of modern brain mapping methods, including 18 F-DG PET scanning and the BOLD signal of functional MRI.
In Schwartz's and Gainer's study of suprachiasmatic nucleus glucose consumption, the suprachiasmatic nucleus was found to have higher glucose consumption during the daytime than during the night. This rhythm of activation was present both with and without environmental light exposure, providing the first evidence for the suprachiasmatic nucleus as an endogenous circadian clock. This research was pivotal in confirming circadian rhythm regulation by the suprachiasmatic nucleus, and aided new techniques to study neural mechanisms. [2]
In 1990, Schwartz et al. began the process of investigating the mechanism of the circadian clock in the suprachiasmatic nucleus by looking at c-Fos, considered the first known suprachiasmatic nucleus clock gene. In order to begin determining the molecular processes that lead to photic entrainment, Schwartz and others analyzed the photic and temporal regulation of the suprachiasmatic nucleus-localized transcriptional regulatory protein c-Fos. They found in albino rats that Fos has altered immunoreactive levels in a phase-dependent manner when exposed to light. This makes Fos a good functional marker for the cellular effects of light, and indicates that it may be a part of the mechanism involved in the photo-entrainment of light. This work contributed to establishing suprachiasmatic nucleus c-Fos as the first photoinducible molecular marker and was critical in the process of determining the necessary substrates of the photic entrainment pathway in mammals.
The Schwartz research group focused on understanding the neural regulation of circadian rhythmicity in mammals. They focused on tissue, organismal, and supra-organismal levels of analysis to see how individual processes interact in the circadian system to produce observable emergent properties. [1] The Schwartz lab investigated light induced and endogenous gene expression, and the underlying dual oscillatory structure of the circadian pacemaker. [1] His research group has focused on defining the mechanisms by which dysrhythmias occur and how social interactions may impact circuits and cells in the master clock. [8]
Schwartz has also researched the effect of social forces on circadian rhythms. His research, conducted with Matthew J. Paul ad Premananda Indic suggests that cohabitation affects the onset of rhythmicity in hamsters, and that changing the speed of the circadian clock is one mechanism by which social factors could alter daily rhythms. [9] In a 2013 paper co-authored with Guy Bloch, Erik D. Herzog and Joel D. Levine, Schwartz shows that social cues may be critical to the adaptive function of circadian rhythms, and can affect them from colony, to organismal, to cellular levels. [10]
As of 2017, Schwartz is not running a research lab as he is helping with education at Dell Medical School, University of Texas at Austin.
As of 2017, Schwartz resides in Austin with his wife, Randi Eisner. The couple have two children, a daughter, Aliza and a son, Jonathan. [11]
This section of a biography of a living person does not include any references or sources .(May 2019) |
A circadian rhythm, or circadian cycle, is a natural oscillation that repeats roughly every 24 hours. Circadian rhythms can refer to any process that originates within an organism and responds to the environment. Circadian rhythms are regulated by a circadian clock whose primary function is to rhythmically co-ordinate biological processes so they occur at the correct time to maximize the fitness of an individual. Circadian rhythms have been widely observed in animals, plants, fungi and cyanobacteria and there is evidence that they evolved independently in each of these kingdoms of life.
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.
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.
Circadian rhythm sleep disorders (CRSD), also known as circadian rhythm sleep-wake disorders (CRSWD), are a family of sleep disorders which affect the timing of sleep. CRSDs cause a persistent pattern of sleep/wake disturbances that arise either by dysfunction in one's biological clock system, or by misalignment between one's endogenous oscillator and externally imposed cues. As a result of this misalignment, those affected by circadian rhythm sleep disorders can fall asleep at unconventional time points in the day, or experience excessive daytime sleepiness if they resist. These occurrences often lead to recurring instances of disrupted rest and wakefulness, where individuals affected by the disorder are unable to go to sleep and awaken at "normal" times for work, school, and other social obligations. Delayed sleep phase disorder, advanced sleep phase disorder, non-24-hour sleep–wake disorder and irregular sleep–wake rhythm disorder represents the four main types of CRSD.
In the study of chronobiology, entrainment refers to the synchronization of a biological clock to an environmental cycle. An example is the interaction between circadian rhythms and environmental cues, such as light and temperature. Entrainment helps organisms adapt their bodily processes with the timing of a changing environment. For example, entrainment is manifested during travel between time zones, hence why humans experience jet lag.
PER2 is a protein in mammals encoded by the PER2 gene. PER2 is noted for its major role in circadian rhythms.
Period circadian protein homolog 1 is a protein in humans that is encoded by the PER1 gene.
Jürgen Walther Ludwig Aschoff was a German physician, biologist and behavioral physiologist. Together with Erwin Bünning and Colin Pittendrigh, he is considered to be a co-founder of the field of chronobiology.
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.
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.
Thomas S. Kilduff is an American neuroscientist and the director of SRI International's Center for Neuroscience. He specializes in neurobiology related to sleep and wakefulness, and was involved in the discovery of hypocretin, a neuropeptide system that is highly involved in wakefulness regulation.
Hitoshi Okamura is a Japanese scientist who specializes in chronobiology. He is currently a professor of Systems Biology at Kyoto University Graduate School of Pharmaceutical Sciences and the Research Director of the Japan Science Technology Institute, CREST. Okamura's research group cloned mammalian Period genes, visualized clock oscillation at the single cell level in the central clock of the SCN, and proposed a time-signal neuronal pathway to the adrenal gland. He received a Medal of Honor with Purple Ribbon in 2007 for his research and was awarded Aschoff's Ruler for his work on circadian rhythms in rodents. His lab recently revealed the effects of m6A mRNA methylation on the circadian clock, neuronal communications in jet lag, and the role of dysregulated clocks in salt-induced hypertension.
The Society for Research on Biological Rhythms (SRBR) is a learned society and professional association headquartered in the United States created to advance the interests of chronobiology in academia, industry, education, and research. Formed in 1986, the society has around 1,000 members, and runs the associated academic journal, the Journal of Biological Rhythms. In addition to communicating with academic and public audiences on matters related to chronobiology, the society seeks to foster interdisciplinary exchange of ideas and advocates for the need for funding and research in biological rhythms to guide the development of related policies.
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.
Sato Honma is a Japanese chronobiologist who researches the biological mechanisms of circadian rhythms. She mainly collaborates with Ken-Ichi Honma on publications, and both of their primary research focuses are the human circadian clock under temporal isolation and the mammalian suprachiasmatic nucleus (SCN), its components, and associates. Honma is a retired professor at the Hokkaido University School of Medicine in Sapporo, Japan. She received her Ph.D. in physiology from Hokkaido University. She taught physiology at the School of Medicine and then at the Research and Education Center for Brain Science at Hokkaido University. She is currently the director at the Center for Sleep and Circadian Rhythm Disorders at Sapporo Hanazono Hospital and works as a somnologist.
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.
The food-entrainable oscillator (FEO) is a circadian clock that can be entrained by varying the time of food presentation. It was discovered when a rhythm was found in rat activity. This was called food anticipatory activity (FAA), and this is when the wheel-running activity of mice decreases after feeding, and then rapidly increases in the hours leading up to feeding. FAA appears to be present in non-mammals (pigeons/fish), but research heavily focuses on its presence in mammals. This rhythmic activity does not require the suprachiasmatic nucleus (SCN), the central circadian oscillator in mammals, implying the existence of an oscillator, the FEO, outside of the SCN, but the mechanism and location of the FEO is not yet known. There is ongoing research to investigate if the FEO is the only non-light entrainable oscillator in the body.
Martha Ulbrick Gillette is a chronobiologist and neurobiologist with research focusing on the effects of circadian clocks on integrative brain functions metabolism and the molecular mechanisms involved in signaling pathways. She is a fellow of the American Association for the Advancement of Science.
Ken-Ichi Honma is a Japanese chronobiologist who researches the biological mechanisms underlying circadian rhythms. After graduating from Hokkaido University School of Medicine, he practiced clinical psychiatry before beginning his research. His recent research efforts are centered around photic and non-photic entrainment, the structure of circadian clocks, and the ontogeny of circadian clocks. He often collaborates with his wife, Sato Honma, on work involving the mammalian suprachiasmatic nucleus (SCN).
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