M. Amin Arnaout

M. Amin Arnaout, M.D. is a physician-scientist and nephrologist best known for seminal discoveries in the biology and structure of integrin receptors. He is Professor of Medicine at Harvard Medical School and physician and former Chief of Nephrology at the Massachusetts General Hospital (MGH).

M. Amin Arnaout
M. Amin Arnaout
Born
Sidon, Lebanon
NationalityAmerican
Alma materAmerican University of Beirut
Known forIntegrins
AwardsKuwait Prize (2017)
Homer W. Smith Award (2018)
Scientific career
FieldsBiology, Immunology, Medicine, Nephrology, Structural Biology
InstitutionsMassachusetts General Hospital
Harvard Medical School
Children's Hospital Boston
Johns Hopkins University
Academic advisorsFred S. Rosen, MD
Websitewww.massgeneral.org

Research

Dr. Arnaout’s research on the biology and structure of integrins has led to scientific observations that span the entire spectrum from gene discovery to 3-dimensional protein structure to clinical translation. He described an inherited deficiency in leukocyte adhesion in a lead article in the New England Journal of Medicine;[1] defined the biochemical and molecular basis of this disease, which he traced to a deficiency in a family of leukocyte receptors, now known as leukocyte integrins[2][3] and elucidated the role of these cell adhesion molecules in the immune system.[4] He was also the first to determine the crystal structures of integrins.[5][6][7][8][9] His molecular and structural studies in integrins were instrumental in understanding the processes involved in organ development, maintenance of organ architecture and homeostasis in the adult, cancer growth and metastasis, and the response of organs to acute and chronic inflammatory or autoimmune injury. For example, in the kidney, integrins are now known to be critical in maintaining the kidney filtration barrier thus preventing loss of blood and proteins in the urine,[10] and also mediate the respiratory distress observed in kidney failure patients when hemodialyzed using cuprophane membranes.[11] Arnaout's current research aims at translating his discoveries in integrin biology and structure into novel and safer drugs for treating inflammatory, thrombotic, fibrotic and autoimmune diseases and cancer, using structure-based drug design.[12][13]

His research on cell adhesion and integrins has been described as "concomitantly advancing the field one enormous stride,"[14] as "one of those spectacular results that will change a field",[15] a "MIDAS touch to cell signaling"[16] and has been featured in the lay press including the New York Times .

Dr. Arnaout also made important contributions in other scientific fields. He was the first to show that C3 nephritic factor is an autoantibody that activates the alternative complement pathway,[17][18] a finding that suggested the potential of B cell or complement C5 depletion as adjunct therapies in certain forms of kidney inflammation. He was also the first to identify the antigen targeted by autoantibodies in patients with systemic vasculitis,[19] which formed the basis for a routinely used diagnostic assay. He was the first to show that polycystin-1, one of two gene products mutated in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD), is required for the structural integrity of blood vessels,[20] indicating that the early onset of high blood pressure and presence of vascular aneurysms in ADPKD is caused by a primary defect in vascular polycystin-1. In collaborative studies, he also showed that polycystin-2, the other gene product defective in ADPKD, is a TRP-like calcium channel,[21] providing new insights into the molecular pathogenesis of ADPKD and potential pathways to therapeutic interventions.

gollark: I doubt it. There's presumably some intermediate encoding step going on.
gollark: If you have a video recorder program which does that, just take the output and mux out the video stream.
gollark: You can make Desmos draw π multiples on the axes?!
gollark: I can search through them easily enough.
gollark: Why? I have lots of RAM now.

References
  1. N Engl J Med. 1982 Mar 25;306(12):693-9
  2. J Clin Invest. 1984 Jan;73(1):153-9
  3. J Clin Invest. 1984 Oct;74(4):1291-300
  4. Immunol Rev. 1990 Apr;114:145-80
  5. Cell. 1993 Mar 26;72(6):857-67
  6. Cell. 1995 Feb 24;80(4):631-8
  7. Science. 2001 Oct 12;294(5541):339-45
  8. Science. 2002 Apr 5;296(5565):151-5
  9. Current Biology. 2002 May 14;12(10):R340-2
  10. N Engl J Med. 2013 Dec 19;369(25):2416-23
  11. N Engl J Med. 1985 Feb 21;312(8):457-62
  12. J Immunol. 2011 Dec 15;187(12):6393-401
  13. Nat Struct Mol Biol. 2014 Apr;21(4):383-8
  14. Science 294, 316-7 (2001)
  15. SCIENCE VOL 293 7 SEPTEMBER 2001
  16. Nature Reviews, 3, 313 (2002)
  17. J Immunol. 1977 Oct;119(4):1316-20
  18. N Engl J Med. 1977 Jul 21;297(3):144-5
  19. Blood. 1989 Nov 1;74(6):1888-93
  20. Proc Natl Acad Sci U S A. 2000 Feb 15;97(4):1731-6
  21. Proc Natl Acad Sci U S A. 2001 Jan 30;98(3):1182-7
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