Martha Gillette

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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.

Contents

Education and career

Gillette attended Grinnell College, where she received a B.A. in biology. She went on to receive an M.S. in zoology from the University of Hawaiʻi and a Ph.D. in developmental biology from the University of Toronto in 1976. Gillette conducted postdoctoral research at the University of California, Santa Cruz. [1] In 1978, Gillette began her professorship at University of Illinois at Urbana-Champaign where she has remained as both a researcher and a professor. [2]

Research

Gillette's research at the University of Illinois, Urbana-Champaign (UIUC) focuses on the relationship between the suprachiasmatic nucleus (SCN) and cells in the hippocampus, as well as how those interactions are influenced by the changes in the circadian rhythm. Gillette's research has shown that the suprachiasmatic nucleus (SCN) generates ~24h neuronal oscillations in rat hypothalamic brain slice in vitro, [3] and she has investigated temporal windows of sensitivity to circadian phase-shifting by different resetting stimuli, including secondary messengers, hormones, and neuropeptide. [3] Gillette has demonstrated how melatonin, a nonphotic Zeitgeber, can directly reset the rat SCN in vitro, [4] and described how E-box mediated transcriptions of Per1 and Per2 are necessary for proper melatonin signaling during the resetting of SCN clock at dusk. [5] Gillette first discovered that SCN redox state exhibits self-sustained circadian oscillations, which requires the functional molecular clockwork of the Bmal1 gene. [6] This ~24hr redox oscillation of SCN dictates its own neuronal excitability via non-transcriptional modulation of potassium (K+) channel. [6]

Selected publications

Awards and honors

Gillette was named a fellow of the American Association for the Advancement of Science in 1995. [7] In 2004, Gillette received the Mika Salpeter Lifetime Achievement Award from the Society for Neuroscience. [8] [9]

Related Research Articles

<span class="mw-page-title-main">Circadian rhythm</span> Natural internal process that regulates the sleep-wake cycle

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 maximise 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.

<span class="mw-page-title-main">Suprachiasmatic nucleus</span> Part of the brains hypothalamus

The suprachiasmatic nucleus or nuclei (SCN) is a small region of the brain in the hypothalamus, situated directly above the optic chiasm. The SCN is the principal circadian pacemaker in mammals, responsible for generating circadian rhythms. Reception of light inputs from photosensitive retinal ganglion cells allow the SCN 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.

<span class="mw-page-title-main">CREB</span> Class of proteins

CREB-TF is a cellular transcription factor. It binds to certain DNA sequences called cAMP response elements (CRE), thereby increasing or decreasing the transcription of the genes. CREB was first described in 1987 as a cAMP-responsive transcription factor regulating the somatostatin gene.

Melatonin receptors are G protein-coupled receptors (GPCR) which bind melatonin. Three types of melatonin receptors have been cloned. The MT1 (or Mel1A or MTNR1A) and MT2 (or Mel1B or MTNR1B) receptor subtypes are present in humans and other mammals, while an additional melatonin receptor subtype MT3 (or Mel1C or MTNR1C) has been identified in amphibia and birds. The receptors are crucial in the signal cascade of melatonin. In the field of chronobiology, melatonin has been found to be a key player in the synchrony of biological clocks. Melatonin secretion by the pineal gland has circadian rhythmicity regulated by the suprachiasmatic nucleus (SCN) found in the brain. The SCN functions as the timing regulator for melatonin; melatonin then follows a feedback loop to decrease SCN neuronal firing. The receptors MT1 and MT2 control this process. Melatonin receptors are found throughout the body in places such as the brain, the retina of the eye, the cardiovascular system, the liver and gallbladder, the colon, the skin, the kidneys, and many others. In 2019, X-ray crystal and cryo-EM structures of MT1 and MT2 were reported.

<span class="mw-page-title-main">NPAS2</span> Protein-coding gene in the species Homo sapiens

Neuronal PAS domain protein 2 (NPAS2) also known as member of PAS protein 4 (MOP4) is a transcription factor protein that in humans is encoded by the NPAS2 gene. NPAS2 is paralogous to CLOCK, and both are key proteins involved in the maintenance of circadian rhythms in mammals. In the brain, NPAS2 functions as a generator and maintainer of mammalian circadian rhythms. More specifically, NPAS2 is an activator of transcription and translation of core clock and clock-controlled genes through its role in a negative feedback loop in the suprachiasmatic nucleus (SCN), the brain region responsible for the control of circadian rhythms.

<span class="mw-page-title-main">PER3</span> Protein and coding gene in humans

The PER3 gene encodes the period circadian protein homolog 3 protein in humans. PER3 is a paralog to the PER1 and PER2 genes. It is a circadian gene associated with delayed sleep phase syndrome in humans.

<span class="mw-page-title-main">PER2</span> Protein-coding gene in the species Homo sapiens

PER2 is a protein in mammals encoded by the PER2 gene. PER2 is noted for its major role in circadian rhythms.

Light effects on circadian rhythm are the effects that light has on circadian rhythm.

<span class="mw-page-title-main">Jürgen Aschoff</span>

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.

Steven M. Reppert is an American neuroscientist known for his contributions to the fields of chronobiology and neuroethology. His research has focused primarily on the physiological, cellular, and molecular basis of circadian rhythms in mammals and more recently on the navigational mechanisms of migratory monarch butterflies. He was the Higgins Family Professor of Neuroscience at the University of Massachusetts Medical School from 2001 to 2017, and from 2001 to 2013 was the founding chair of the Department of Neurobiology. Reppert stepped down as chair in 2014. He is currently distinguished professor emeritus of neurobiology.

A chronobiotic is an agent that can cause phase adjustment of the circadian rhythm. That is, it is a substance capable of therapeutically entraining or re-entraining long-term desynchronized or short-term dissociated circadian rhythms in mammals, or prophylactically preventing their disruption following an environmental insult such as is caused by rapid travel across several time zones. The most widely recognized chronobiotic is the hormone melatonin, secreted at night in both diurnal and nocturnal species.

<span class="mw-page-title-main">Douglas G. McMahon</span>

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.

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.

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.

<span class="mw-page-title-main">Michael Harvey Hastings</span> British neuroscientist

Michael Harvey Hastings is a British neuroscientist who works at the Medical Research Council MRC Laboratory of Molecular Biology (LMB) in Cambridge, UK. Hastings is known for his contributions to the current understanding of biological clocks in mammals and marine invertebrates.

<span class="mw-page-title-main">Sato Honma</span>

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.

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.

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, in work involving the mammalian suprachiasmatic nucleus (SCN), its components, and associated topics.

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 was 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.

References

  1. "Gillette webpage".
  2. D'ALESSIO, JEFF (22 April 2021). "MY CAMPUS: 2021 Beckman Vision & Spirit Award winner Martha Gillette". The News-Gazette. Retrieved 2021-05-06.
  3. 1 2 Gillette, Martha U.; Medanic, Marija; McArthur, Angela J.; Liu, Chen; Ding, Jian M.; Faiman, Lia E.; Weber, E. Todd; Tcheng, Thomas K.; Gallman, Eve A. (2007-09-28), Chadwick, Derek J.; Ackrill, Kate (eds.), "Intrinsic Neuronal Rhythms in the Suprachiasmatic Nuclei and their Adjustment", Novartis Foundation Symposia, Chichester, UK: John Wiley & Sons, Ltd., vol. 183, pp. 134–153, doi:10.1002/9780470514597.ch8, ISBN   978-0-470-51459-7, PMID   7656683 , retrieved 2021-05-06
  4. McArthur, Angela J.; Gillette, Martha U.; Prosser, Rebecca A. (1991-11-22). "Melatonin directly resets the rat suprachiasmatic circadian clock in vitro". Brain Research. 565 (1): 158–161. doi:10.1016/0006-8993(91)91748-P. ISSN   0006-8993. PMID   1773352. S2CID   15501781.
  5. Kandalepas, Patty C.; Mitchell, Jennifer W.; Gillette, Martha U. (2016-06-30). Yamazaki, Shin (ed.). "Melatonin Signal Transduction Pathways Require E-Box-Mediated Transcription of Per1 and Per2 to Reset the SCN Clock at Dusk". PLOS ONE. 11 (6): e0157824. Bibcode:2016PLoSO..1157824K. doi: 10.1371/journal.pone.0157824 . ISSN   1932-6203. PMC   4928778 . PMID   27362940.
  6. 1 2 Wang, T. A.; Yu, Y. V.; Govindaiah, G.; Ye, X.; Artinian, L.; Coleman, T. P.; Sweedler, J. V.; Cox, C. L.; Gillette, M. U. (2012-08-17). "Circadian Rhythm of Redox State Regulates Excitability in Suprachiasmatic Nucleus Neurons". Science. 337 (6096): 839–842. Bibcode:2012Sci...337..839W. doi:10.1126/science.1222826. ISSN   0036-8075. PMC   3490628 . PMID   22859819.
  7. "Historic Fellows | American Association for the Advancement of Science". www.aaas.org. Retrieved 2022-04-13.
  8. "Mika Salpeter Lifetime Achievement Award". www.sfn.org. Retrieved 2022-04-13.
  9. Parsell, Diana (1995-10-27). "Inside AAAS". Science. 270 (5236): 647–649. Bibcode:1995Sci...270..647P. doi:10.1126/science.270.5236.647. ISSN   0036-8075. S2CID   220102677.