Michael Levin (biologist)

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Michael Levin
Michael Levin.jpg
Born1969 (age 5455)
CitizenshipUnited States
Alma mater Tufts University (BS)
Harvard University (PhD) [1]
Known for Left-right asymmetry, Bioelectricity, morphogenesis, xenobots
AwardsCozzarelli prize (2020) [2]
Scientific career
Fields Developmental biology, synthetic biology
Institutions Forsyth Institute [1]
Tufts University [3]
Wyss Institute
Harvard Medical School
Doctoral advisor Clifford Tabin
Website www.drmichaellevin.org

Michael Levin is an American developmental and synthetic biologist at Tufts University, where he is the Vannevar Bush Distinguished Professor. [3] Levin is a director of the Allen Discovery Center at Tufts University and Tufts Center for Regenerative and Developmental Biology. [3] He is also co-director of the Institute for Computationally Designed Organisms [4] with Josh Bongard.

Contents

Early life

Michael Levin was born in Moscow, USSR, in 1969, in a Jewish family. [5] His parents faced antisemitism in the Soviet Union, and in 1978 took advantage of a visa program for Soviet Jews and moved the family to Lynn, Massachusetts. [5] Levin's father was a computer programmer and worked for the Soviet weather service; [5] his mother was a concert pianist. [6]

Levin's family immigration was sponsored by Temple Sinai in Marblehead, Massachusetts. His family is still members of Temple Sinai. [6] Levin stated that "... I've always lived within about a mile radius of where we landed in '78." [6]

Career

Levin received dual bachelor's degrees in computer science and biology from Tufts University, and a Ph. D. in genetics from Harvard University (working in the lab of Clifford Tabin). His post-doctoral training was in the Cell Biology department of Harvard School of Medicine with Mark Mercola. [7] Levin first established his independent lab at the Forsyth Institute in 2000. His research interests include: bioelectrical signals by which cells communicate to serve the dynamic anatomical needs of the organism during development, regeneration, and cancer suppression; basal cognition and intelligence in diverse unconventional substrates; and top-down control of form and function across scales in biology. He moved his group to Tufts in 2009. [8] In 2010, he also became an associate member of the Wyss Institute of Harvard Medical School. [9]

A xenobot design discovered in simulation (left) and the deployed organism (right) built from frog skin (green) and heart muscle (red). A xenobot in simulation and reality.png
A xenobot design discovered in simulation (left) and the deployed organism (right) built from frog skin (green) and heart muscle (red).

He is known for co-discovering the Xenobots, "Living robots made from frog skin cells can sense their environment". [10] This research is focused on development of a multiplexed, microfluidic, Xenopus embryo culture system that will enable discovery of new drug targets and development of therapeutics when combined with multiomics and an integrated bioinformatics pipeline. This work was funded by the DARPA L2M program.

As of 2021, Levin's lab is working on synthetic biology applications of bioelectricity for cellular control; development of a bioinformatics of shape, AI tools for discovery and testing of algorithmic models linking molecular-genetic data to morphogenesis; using techniques from AI, computational neuroscience, and cognitive science to make models of morphogenesis. [11]

Levin is co-editor in chief of Bioelectricity, founding associate editor of Collective Intelligence, and is on editorial advisory board of Laterality journals. [3]

Awards and honors

Source: [12]

Publications

Michael Levin has published more than 350 papers; the full list can be found on his Google Scholar page [13] or in his official biography at Tufts website [14] or on his official website. [15] [12] Some of the most cited papers:

Related Research Articles

Developmental biology is the study of the process by which animals and plants grow and develop. Developmental biology also encompasses the biology of regeneration, asexual reproduction, metamorphosis, and the growth and differentiation of stem cells in the adult organism.

Morphogenesis is the biological process that causes a cell, tissue or organism to develop its shape. It is one of three fundamental aspects of developmental biology along with the control of tissue growth and patterning of cellular differentiation.

<span class="mw-page-title-main">Cilium</span> Organelle found on eukaryotic cells

The cilium is a membrane-bound organelle found on most types of eukaryotic cell. Cilia are absent in bacteria and archaea. The cilium has the shape of a slender threadlike projection that extends from the surface of the much larger cell body. Eukaryotic flagella found on sperm cells and many protozoans have a similar structure to motile cilia that enables swimming through liquids; they are longer than cilia and have a different undulating motion.

<span class="mw-page-title-main">Planarian</span> Flatworms of the Turbellaria class

Planarians (triclads) are free-living flatworms of the class Turbellaria, order Tricladida, which includes hundreds of species, found in freshwater, marine, and terrestrial habitats. Planarians are characterized by a three-branched intestine, including a single anterior and two posterior branches. Their body is populated by adult stem cells called neoblasts, which planarians use for regenerating missing body parts. Many species are able to regenerate any missing organ, which has made planarians a popular model in research of regeneration and stem cell biology. The genome sequences of several species are available, as are tools for molecular biology analysis.

<span class="mw-page-title-main">Regeneration (biology)</span> Biological process of renewal, restoration, and tissue growth

Regeneration in biology is the process of renewal, restoration, and tissue growth that makes genomes, cells, organisms, and ecosystems resilient to natural fluctuations or events that cause disturbance or damage. Every species is capable of regeneration, from bacteria to humans. Regeneration can either be complete where the new tissue is the same as the lost tissue, or incomplete after which the necrotic tissue becomes fibrotic.

<span class="mw-page-title-main">Symmetry in biology</span> Geometric symmetry in living beings

Symmetry in biology refers to the symmetry observed in organisms, including plants, animals, fungi, and bacteria. External symmetry can be easily seen by just looking at an organism. For example, the face of a human being has a plane of symmetry down its centre, or a pine cone displays a clear symmetrical spiral pattern. Internal features can also show symmetry, for example the tubes in the human body which are cylindrical and have several planes of symmetry.

Biological immortality is a state in which the rate of mortality from senescence is stable or decreasing, thus decoupling it from chronological age. Various unicellular and multicellular species, including some vertebrates, achieve this state either throughout their existence or after living long enough. A biologically immortal living being can still die from means other than senescence, such as through injury, poison, disease, predation, lack of available resources, or changes to environment.

Lefty are a class of proteins that are closely related members of the TGF-beta superfamily of growth factors. These proteins are secreted and play a role in left-right asymmetry determination of organ systems during development. Mutations of the genes encoding these proteins have been associated with left-right axis malformations, particularly in the heart and lungs.

Within the field of developmental biology, one goal is to understand how a particular cell develops into a final cell type, known as fate determination. Within an embryo, several processes play out at the cellular and tissue level to create an organism. These processes include cell proliferation, differentiation, cellular movement and programmed cell death. Each cell in an embryo receives molecular signals from neighboring cells in the form of proteins, RNAs and even surface interactions. Almost all animals undergo a similar sequence of events during very early development, a conserved process known as embryogenesis. During embryogenesis, cells exist in three germ layers, and undergo gastrulation. While embryogenesis has been studied for more than a century, it was only recently that scientists discovered that a basic set of the same proteins and mRNAs are involved in embryogenesis. Evolutionary conservation is one of the reasons that model systems such as the fly, the mouse, and other organisms are used as models to study embryogenesis and developmental biology. Studying model organisms provides information relevant to other animals, including humans. While studying the different model systems, cells fate was discovered to be determined via multiple ways, two of which are by the combination of transcription factors the cells have and by the cell-cell interaction. Cells' fate determination mechanisms were categorized into three different types, autonomously specified cells, conditionally specified cells, or syncytial specified cells. Furthermore, the cells' fate was determined mainly using two types of experiments, cell ablation and transplantation. The results obtained from these experiments, helped in identifying the fate of the examined cells.

<span class="mw-page-title-main">Cerberus (protein)</span> Protein found in humans

Cerberus is a protein that in humans is encoded by the CER1 gene. Cerberus is a signaling molecule which contributes to the formation of the head, heart and left-right asymmetry of internal organs. This gene varies slightly from species to species but its overall functions seem to be similar.

<span class="mw-page-title-main">Nodal homolog</span> Mammalian protein found in Homo sapiens

Nodal homolog is a secretory protein that in humans is encoded by the NODAL gene which is located on chromosome 10q22.1. It belongs to the transforming growth factor beta superfamily. Like many other members of this superfamily it is involved in cell differentiation in early embryogenesis, playing a key role in signal transfer from the primitive node, in the anterior primitive streak, to lateral plate mesoderm (LPM).

<span class="mw-page-title-main">Cell polarity</span> Polar morphology of a cell, a specific orientation of the cell structure

Cell polarity refers to spatial differences in shape, structure, and function within a cell. Almost all cell types exhibit some form of polarity, which enables them to carry out specialized functions. Classical examples of polarized cells are described below, including epithelial cells with apical-basal polarity, neurons in which signals propagate in one direction from dendrites to axons, and migrating cells. Furthermore, cell polarity is important during many types of asymmetric cell division to set up functional asymmetries between daughter cells.

<span class="mw-page-title-main">Donald E. Ingber</span> American cell biologist and bioengineer (born 1956)

Donald E. Ingber is an American cell biologist and bioengineer. He is the founding director of the Wyss Institute for Biologically Inspired Engineering at Harvard University, the Judah Folkman Professor of Vascular Biology at Harvard Medical School and Boston Children's Hospital, and Professor of Bioengineering at the Harvard John A. Paulson School of Engineering and Applied Sciences. He is also a member of the American Institute for Medical and Biological Engineering, the National Academy of Engineering, the National Academy of Medicine, the National Academy of Inventors, and the American Academy of Arts and Sciences.

Andrea Hilary Brand is the Herchel Smith Professor of Molecular Biology and a Fellow of Jesus College, Cambridge. She heads a lab investigating nervous system development at the Gurdon Institute and the Department of Physiology, Development and Neuroscience. She developed the GAL4/UAS system with Norbert Perrimon which has been described as “a fly geneticist's Swiss army knife”.

<span class="mw-page-title-main">Clifford Tabin</span> American geneticist

Clifford James Tabin is chairman of the Department of Genetics at Harvard Medical School.

<span class="mw-page-title-main">Developmental bioelectricity</span> Electric current produced in living cells

Developmental bioelectricity is the regulation of cell, tissue, and organ-level patterning and behavior by electrical signals during the development of embryonic animals and plants. The charge carrier in developmental bioelectricity is the ion rather than the electron, and an electric current and field is generated whenever a net ion flux occurs. Cells and tissues of all types use flows of ions to communicate electrically. Endogenous electric currents and fields, ion fluxes, and differences in resting potential across tissues comprise a signalling system. It functions along with biochemical factors, transcriptional networks, and other physical forces to regulate cell behaviour and large-scale patterning in processes such as embryogenesis, regeneration, and cancer suppression.

In developmental biology, left-right asymmetry is the process in early embryonic development that breaks the normal symmetry in the bilateral embryo. In vertebrates, left-right asymmetry is established early in development at a structure called the left-right organizer and leads to activation of different signalling pathways on the left and right of the embryo. This in turn causes several organs in adults to develop LR asymmetry, such as the tilt of the heart, the different number of lung lobes on each side of the body, and the position of the stomach and spleen on the right side of the body. If this process does not occur correctly in humans it can result in heterotaxy or situs inversus.

<span class="mw-page-title-main">Xenobot</span> Artificial organism

Xenobots, named after the African clawed frog, are synthetic lifeforms that are designed by computers to perform some desired function and built by combining together different biological tissues. There is debate among scientists whether xenobots are robots, organisms, or something else entirely.

Barry James Thompson is an Australian and British developmental biologist and cancer biologist. Thompson is known for identifying genes, proteins and mechanisms involved in epithelial polarity, morphogenesis and cell signaling via the Wnt and Hippo signaling pathways, which have key roles in human cancer.

The Wyss Institute for Biologically Inspired Engineering is a cross-disciplinary research institute at Harvard University focused on bridging the gap between academia and industry by drawing inspiration from nature's design principles to solve challenges in health care and the environment. It is focused on the field of biologically inspired engineering to be distinct from bioengineering and biomedical engineering. The institute also has a focus on applications, intellectual property generation, and commercialization.

References

  1. 1 2 "Michael Levin Brief Bio". loop.frontiersin.org.
  2. "PNAS Announces Six 2020 Cozzarelli Prize Recipients". National Academy of Sciences.
  3. 1 2 3 4 "Tufts University: The Levin Lab" . Retrieved 7 June 2021.
  4. "Institute for Computationally Designed Organisms" . Retrieved 17 January 2022.
  5. 1 2 3 "Persuading the Body to Regenerate Its Limbs". The New Yorker. 29 April 2021.
  6. 1 2 3 "Oral History Interviews with Michael Levin". American Institute of Physics. 24 September 2021.
  7. "Mark Mercola". 19 March 2018. Retrieved 17 January 2022.
  8. "Levin Lab". Tufts University: The Levin Lab. Retrieved 20 January 2022.
  9. "Wyss Institute: Michael Levin". Wyss Institute: Michael Levin. 28 March 2017. Retrieved 20 January 2022.
  10. "Living robots made from frog skin cells can sense their environment". New Scientist.
  11. "Levin's Lab: New directions" . Retrieved 7 June 2021.
  12. 1 2 "Michael Levin Biographical Sketch" (PDF).
  13. "Michael Levin GS". Google Scholar ML biologist. Retrieved 20 January 2022.
  14. "Levin's Lab Publications".
  15. "Peer-Reviewed Papers on Levin's website".