Michelle Antoine

Last updated
Michelle Antoine
Michelle Antoine.jpg
Michelle Antoine in 2021
NationalityTrinidadian
Alma mater Albert Einstein College of Medicine
Spelman College
Scientific career
Institutions National Institute on Alcohol Abuse and Alcoholism

Michelle Antoine is a Trinidadian neuroscientist. She is acting chief of the section on neural circuits in the National Institute on Alcohol Abuse and Alcoholism (NIAAA). [1] Her research has redefined the classical notion of excitatory-inhibitory balance and its role in autism. [2] She continues to study the synaptic and circuit pathways that contribute to nervous system disorders, autism spectrum disorder in particular. [3]

Contents

Background and education

Michelle Antoine was born in Trinidad and Tobago, where she went to the all-female Bishop Anstey High School. [4] After graduation from high school, she attended Spelman College where she received a Bachelor’s of Science in Biology and Mathematics. Following her graduation from Spelman College, Antoine went on to attend graduate school at Albert Einstein College of Medicine. [4]

Antoine completed her postdoctoral training at the University of California, Berkeley, in Daniel Feldman’s laboratory, where she was a Miller Research Fellow and a UC President’s Postdoctoral Fellow. [5]

Career and research

Antoine wrote her dissertation about a causative link between inner ear defects and long-term striatal dysfunction. [5] At Albert Einstein College of Medicine, Antoine noticed unusual hyper activity in mice. Antoine later found that inner ear dysfunction in mice has a direct causal relationship with neurological changes that increase hyperactivity. With these findings, Antoine provided two brain proteins as potential intervention targets for behavioral abnormalities. These proteins include pERK (phosphorylated extracellular signal-regulated kinase) and pCREB (phospho-cAMP response-element binding protein). [6]

As a Miller Postdoctoral Fellow, Antoine worked with Daniel Feldman's team to analyze four mouse models in relation to the 'signaling imbalance theory', which is a well known hypothesis about the origin of autism in the brain. This theory states that the brains of autistic people have an excess of excitatory brain activity, but not enough inhibitory signals to counterbalance. As a result, the neurons in brains of autistic people fire at a higher rate than normal, which leads to further motor disabilities, sensory issues, and additional autism traits. The team negated the original hypothesis of this theory, and instead proved that this imbalance is a compensatory effect, as opposed to the origin of autism. They found that the difference in the signals in the autism brains is of a type that stabilizes neurons’ firing rates rather than increasing them, which is suggestive of a compensatory response. [7] [8]

Antoine currently works at the NIAAA, where her lab studies normal brains versus diseased brains and brain circuit function from the lens of developmental disabilities such as autism spectrum disorder. [9]

Related Research Articles

<span class="mw-page-title-main">Behavioral neuroscience</span> Field of study

Behavioral neuroscience, also known as biological psychology, biopsychology, or psychobiology, is the application of the principles of biology to the study of physiological, genetic, and developmental mechanisms of behavior in humans and other animals.

<span class="mw-page-title-main">Neural circuit</span> Network or circuit of neurons

A neural circuit is a population of neurons interconnected by synapses to carry out a specific function when activated. Multiple neural circuits interconnect with one another to form large scale brain networks.

Binaural fusion or binaural integration is a cognitive process that involves the combination of different auditory information presented binaurally, or to each ear. In humans, this process is essential in understanding speech as one ear may pick up more information about the speech stimuli than the other.

<span class="mw-page-title-main">Neurexin</span> Protein family

Neurexins (NRXN) are a family of presynaptic cell adhesion proteins that have roles in connecting neurons at the synapse. They are located mostly on the presynaptic membrane and contain a single transmembrane domain. The extracellular domain interacts with proteins in the synaptic cleft, most notably neuroligin, while the intracellular cytoplasmic portion interacts with proteins associated with exocytosis. Neurexin and neuroligin "shake hands," resulting in the connection between the two neurons and the production of a synapse. Neurexins mediate signaling across the synapse, and influence the properties of neural networks by synapse specificity. Neurexins were discovered as receptors for α-latrotoxin, a vertebrate-specific toxin in black widow spider venom that binds to presynaptic receptors and induces massive neurotransmitter release. In humans, alterations in genes encoding neurexins are implicated in autism and other cognitive diseases, such as Tourette syndrome and schizophrenia.

<span class="mw-page-title-main">Neuroligin</span> Protein

Neuroligin (NLGN), a type I membrane protein, is a cell adhesion protein on the postsynaptic membrane that mediates the formation and maintenance of synapses between neurons. Neuroligins act as ligands for β-neurexins, which are cell adhesion proteins located presynaptically. Neuroligin and β-neurexin "shake hands", resulting in the connection between two neurons and the production of a synapse. Neuroligins also affect the properties of neural networks by specifying synaptic functions, and they mediate signalling by recruiting and stabilizing key synaptic components. Neuroligins interact with other postsynaptic proteins to localize neurotransmitter receptors and channels in the postsynaptic density as the cell matures. Additionally, neuroligins are expressed in human peripheral tissues and have been found to play a role in angiogenesis. In humans, alterations in genes encoding neuroligins are implicated in autism and other cognitive disorders. Antibodies in a mother from previous male pregnancies against neuroligin 4 from the Y chromosome increase the probability of homosexuality in male offspring.

<span class="mw-page-title-main">TSHZ3</span> Protein-coding gene in the species Homo sapiens

Teashirt homolog 3 is a protein that in humans is encoded by the TSHZ3 gene. In mice, it is a necessary part of the neural circuitry that controls breathing. The gene is also a homolog of the Drosophila melanogaster teashirt gene, which encodes a zinc finger transcription factor important for development of the trunk.

Michael Greenberg is an American neuroscientist who specializes in molecular neurobiology. He served as the Chair of the Department of Neurobiology at Harvard Medical School from 2008 to 2022.

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

Neurogenomics is the study of how the genome of an organism influences the development and function of its nervous system. This field intends to unite functional genomics and neurobiology in order to understand the nervous system as a whole from a genomic perspective.

<span class="mw-page-title-main">Jacqueline Crawley</span> American behavioral neuroscientist

Jacqueline N. Crawley is an American behavioral neuroscientist and an expert on rodent behavioral analysis. Since July 2012, she is the Robert E. Chason Chair in Translational Research in the MIND Institute and professor of psychiatry and behavioral sciences at the University of California, Davis School of Medicine in Sacramento. Previously, from 1983–2012, she was chief of the Laboratory of Behavioral Neuroscience in the intramural program of the National Institute of Mental Health. Her translational research program focuses on testing hypotheses about the genetic causes of autism spectrum disorders and discovering treatments for the diagnostic symptoms of autism, using mouse models. She has published more than 275 peer-reviewed articles in scientific journals and 110 review articles and book chapters. According to Scopus, her works have been cited over 36,000 times, giving her an h-index of 99. She has co-edited 4 books and is the author of What's Wrong With my Mouse? Behavioral Phenotyping of Transgenic and Knockout Mice, which was very well received.

The development of an animal model of autism is one approach researchers use to study potential causes of autism. Given the complexity of autism and its etiology, researchers often focus only on single features of autism when using animal models.

Autism's symptoms result from maturation-related changes in various systems of the brain. Although it is not well understood how autism occurs, there have been attempts to describe the mechanisms involved. Conceptually, one can divide its development into two areas: the pathophysiology of brain structures and processes associated with autism, and the neuropsychological linkages between brain structures and behaviors. The behaviors appear to have multiple pathophysiologies.

<span class="mw-page-title-main">Nicola Allen</span> British glial biologist

Nicola J. Allen is a British neuroscientist. Allen studies the role of astrocytes in brain development, homeostasis, and aging. Her work uncovered the critical roles these cells play in brain plasticity and disease. Allen is currently an associate professor at the Salk Institute for Biological Studies and Hearst Foundation Development Chair.

R. Suzanne Zukin is an American neuroscientist and a professor of neuroscience who directs a research lab as a F. M. Kirby Chair in Neural Repair and Protection and director of the Neuropsychopharmacology Center at Albert Einstein College of Medicine. Zukin's areas of research include neurodegenerative disorders, Ischemia, Epigenetics and Autism and uses molecular biology approaches to research these disorders. Zukin has made seminal contributions to the understanding of NMDA and AMPA receptor function and activity.

Tom Otis is an American researcher, academic and author. He is the Chief Scientific Officer at the Sainsbury Wellcome Centre for Neural Circuits and Behaviour and holds a Professorship in Neuroscience at University College London.

Nadine Gogolla is a Research Group Leader at the Max Planck Institute of Neurobiology in Martinsried, Germany as well as an Associate Faculty of the Graduate School for Systemic Neuroscience. Gogolla investigates the neural circuits underlying emotion to understand how the brain integrates external cues, feeling states, and emotions to make calculated behavioral decisions. Gogolla is known for her discovery using machine learning and two-photon microscopy to classify mouse facial expressions into emotion-like categories and correlate these facial expressions with neural activity in the insular cortex.

Camilla Bellone is an Italian neuroscientist and assistant professor in the Department of Basic Neuroscience at the University of Geneva, in Switzerland. Bellone's laboratory explores the molecular mechanisms and neural circuits underlying social behavior and probes how defects at the molecular and circuit level give rise to psychiatric disease states such as Autism Spectrum Disorders. 

Lauren Orefice is an American neuroscientist and assistant professor in the Department of Molecular Biology at Massachusetts General Hospital and in the Department of Genetics at Harvard Medical School. Orefice has made innovative discoveries about the role of peripheral nerves and sensory hypersensitivity in the development of Autism-like behaviors. Her research now focuses on exploring the basic biology of somatosensory neural circuits for both touch and gastrointestinal function in order to shed light on how peripheral sensation impacts brain development and susceptibility to diseases like Autism Spectrum Disorders.

Michelle Gray is an American neuroscientist and assistant professor of neurology and neurobiology at the University of Alabama Birmingham. Gray is a researcher in the study of the biological basis of Huntington's disease (HD). In her postdoctoral work, she developed a transgenic mouse line, BACHD, that is now used worldwide in the study of HD. Gray's research now focuses on the role of glial cells in HD. In 2020 Gray was named one of the 100 Inspiring Black Scientists in America by Cell Press. She is also a member of the Hereditary Disease Foundation’s scientific board.

Mary Kay Lobo is an American psychiatric neuroscientist who is a Professor of Neurobiology at the University of Maryland School of Medicine. Her research considers the molecular mechanisms that underpin drug addiction and depression. She was named a finalist in the 2011 Blavatnik Awards for Young Scientists.

References

  1. "Michelle Antoine, PhD | National Institute on Alcohol Abuse and Alcoholism (NIAAA)". www.niaaa.nih.gov. Retrieved 2021-12-01.
  2. Antoine, Michelle W.; Langberg, Tomer; Schnepel, Philipp; Feldman, Daniel E. (2019-02-20). "Increased Excitation-Inhibition Ratio Stabilizes Synapse and Circuit Excitability in Four Autism Mouse Models". Neuron. 101 (4): 648–661.e4. doi:10.1016/j.neuron.2018.12.026. ISSN   1097-4199. PMC   6733271 . PMID   30679017.
  3. "Michelle ANTOINE | University of California, Berkeley, CA | UCB | Helen Wills Neuroscience Institute". ResearchGate. Retrieved 2021-11-29.
  4. 1 2 "Episode 12: Michelle Antoine, PhD". Conjugate: Illustration and Science Blog. Retrieved 2021-12-01.
  5. 1 2 "Michelle W. Antoine | PPFP". ppfp.ucop.edu. Retrieved 2021-12-01.
  6. "Inner-ear disorders may cause hyperactivity". ScienceDaily. Retrieved 2021-12-01.
  7. "Study Reveals 'Inhibition' Theory of Autism is Wrong". Neuroscience News. 2019-01-21. Retrieved 2021-12-01.
  8. "Four sets of mice call popular autism theory into question". Spectrum | Autism Research News. 2019-02-25. Retrieved 2021-12-01.
  9. Bozelos, Panos. "World Wide ✈️ Neuroscience". www.world-wide.org. Retrieved 2021-12-01.