Hans G. Boman

Last updated
Hans G. Boman
Born(1924-08-16)16 August 1924
Died3 December 2008(2008-12-03) (aged 84)
Nationality Swedish
Alma mater Stockholm University
Scientific career
Fields Biology
Institutions Uppsala University, Umeå University, Stockholm University
Doctoral advisor Arne Tiselius

Hans Gustaf Boman (1924-2008) was a Swedish microbiologist with a special focus on innate immunity. Boman was born on 16 August 1924 in Engelbrekt Parish, Stockholm, Sweden, and died on 3 December 2008. Boman's pioneering research on insect immunity formed the basis for the Nobel Prize in Physiology or Medicine that was awarded to Jules Hoffman in 2011. [1]

Contents

Biography

Hans G. Boman graduated from Uppsala University, where he obtained his PhD in biochemistry in 1958 with Professor Arne Tiselius. He completed his post-doctoral studies at the Rockefeller Institute in New York. During his stay in New York, he married Anita Boman, who then became his main research partner. They returned to Sweden and Uppsala University in 1960 where he established a research group at the Department of Biochemistry. In 1966 Boman was appointed professor of microbiology at Umeå University. Between 1966 and 1976 he built up the Department of Microbiology at Umeå University, where his research focused on mechanisms for bacterial antibiotic resistance. Boman combined physiological, molecular, biochemical and genetic methods in a way that was unique at that time. In 1976, Boman became professor of microbiology at Stockholm University where his work in moths identified the first antimicrobial peptides of animals in 1981. He later moved to the Microbiological and Tumor Biology Center at the Karolinska Institute in 1997. At the Karolinska Institute, he identified a disease that occurs in connection with antimicrobial peptides. [2]

Research

During his time in Umeå, Boman collaborated with Bertil Rasmusson at the Department of Genetics. In a famous back-and-forth exchange, Boman put forth unto Rasmusson: "'Do fruit flies ever get sick?' (Boman). 'Very rarely,' (Rasmuson). 'Then they must have an efficient immune response!' (Boman)." Their work asked how insects can survive infections without having a system of B cells and T cells, at the time thought to be essential for immune defence. [3] They examined the immune system of fruit flies and could show that flies that were once infected with a non-lethal dose of the bacterium Pseudomonas survived a second higher dose while flies that received the same high dose for the first time died.

Boman continued to investigate the immune response of insects, focussing on the proteins induced by immune challenge. This posed technical challenges that required a larger insect capable of donating more hemolymph (insect blood). His eventual choice was the Cecropia silk moth ( Hyalophora cecropia ).

In 1981, Boman's group published the protein structure of the antimicrobial peptide cecropin, the first animalian antimicrobial peptide described. [4] With techniques for cloning genes, Boman's group was able to continue studies on immune genes in Cecropia. At the same time, the field of innate immunity rapidly expanded, benefitting from the genetic tools available in Drosophila in the search to understand how insect immunity recognizes and signals following infection. From these initial studies, a number of insect antimicrobial peptides and other immune proteins were characterized, and these peptides have been used extensively as readouts of immune challenge. Owing to Boman's discovery, immune-inducible peptides were used to identify competent or deficient immune responses, ultimately leading to the Nobel Prize for Physiology or Medicine being awarded to Jules Hoffmann for his work on insect immune signalling. [5]

Awards and honors

Boman was awarded the Fernström Prize for outstanding work in medicine in 2000. The Nordic scientific community mourned his loss in 2008, both with a posthumous acknowledgement of his lifetime's achievements in 2009, [6] and by hosting the “Hans G. Boman” symposium held by Stockholm University on the 10-year anniversary of his death. [7] In 2015, a family of immune-inducible peptides in Drosophila was named the "Bomanins" in Boman's honour. [8]

Related Research Articles

<i>Drosophila melanogaster</i> Species of fruit fly

Drosophila melanogaster is a species of fly in the family Drosophilidae. The species is often referred to as the fruit fly or lesser fruit fly, or less commonly the "vinegar fly", "pomace fly", or "banana fly". In the wild, D. melanogaster are attracted to rotting fruit and fermenting beverages, and are often found in orchards, kitchens and pubs.

<span class="mw-page-title-main">Günter Blobel</span> German American biologist (1999 Nobel Prize)

Günter Blobel was a Silesian German and American biologist and 1999 Nobel Prize laureate in Physiology for the discovery that proteins have intrinsic signals that govern their transport and localization in the cell.

<span class="mw-page-title-main">Toll-like receptor</span> Pain receptors and inflammation

Toll-like receptors (TLRs) are a class of proteins that play a key role in the innate immune system. They are single-spanning receptors usually expressed on sentinel cells such as macrophages and dendritic cells, that recognize structurally conserved molecules derived from microbes. Once these microbes have reached physical barriers such as the skin or intestinal tract mucosa, they are recognized by TLRs, which activate immune cell responses. The TLRs include TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, TLR12, and TLR13. Humans lack genes for TLR11, TLR12 and TLR13 and mice lack a functional gene for TLR10. The receptors TLR1, TLR2, TLR4, TLR5, TLR6, and TLR10 are located on the cell membrane, whereas TLR3, TLR7, TLR8, and TLR9 are located in intracellular vesicles.

<span class="mw-page-title-main">Ralph M. Steinman</span> Canadian immunologist and cell biologist

Ralph Marvin Steinman was a Canadian physician and medical researcher at Rockefeller University, who in 1973 discovered and named dendritic cells while working as a postdoctoral fellow in the laboratory of Zanvil A. Cohn, also at Rockefeller University. Steinman was one of the recipients of the 2011 Nobel Prize in Physiology or Medicine.

<span class="mw-page-title-main">Jules A. Hoffmann</span> French biologist

Jules Alphonse Nicolas Hoffmann is a Luxembourg-born French biologist. During his youth, growing up in Luxembourg, he developed a strong interest in insects under the influence of his father, Jos Hoffmann. This eventually resulted in the younger Hoffmann's dedication to the field of biology using insects as model organisms. He currently holds a faculty position at the University of Strasbourg. He is a research director and member of the board of administrators of the National Center of Scientific Research (CNRS) in Strasbourg, France. He was elected to the positions of Vice-President (2005-2006) and President (2007-2008) of the French Academy of Sciences. Hoffmann and Bruce Beutler were jointly awarded a half share of the 2011 Nobel Prize in Physiology or Medicine for "their discoveries concerning the activation of innate immunity,". [More specifically, the work showing increased Drosomycin expression following activation of Toll pathway in microbial infection.]

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

Arthropod defensins are a family defensin proteins found in mollusks, insects, and arachnids. These cysteine-rich antibacterial peptides are primarily active against Gram-positive bacteria and fungi in vitro. However Drosophila fruit flies mutant for the fly defensin were more susceptible to infection by the Gram-negative bacteria Providencia burhodogranariea, and resisted infection against Gram-positive bacteria like wild-type flies. It remains to be seen how in vitro activity relates to in vivo function. Mutants for the defensin-like antimicrobial peptide Drosomycin were more susceptible to fungi, validating a role for defensin-like peptides in anti-fungal defence.

Priming is the first contact that antigen-specific T helper cell precursors have with an antigen. It is essential to the T helper cells' subsequent interaction with B cells to produce antibodies. Priming of antigen-specific naive lymphocytes occurs when antigen is presented to them in immunogenic form. Subsequently, the primed cells will differentiate either into effector cells or into memory cells that can mount stronger and faster response to second and upcoming immune challenges. T and B cell priming occurs in the secondary lymphoid organs.

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

Cecropins are antimicrobial peptides. They were first isolated from the hemolymph of Hyalophora cecropia, whence the term cecropin was derived. Cecropins lyse bacterial cell membranes; they also inhibit proline uptake and cause leaky membranes.

Richard L. Gallo is an American dermatologist who is a Distinguished Professor and founding Chairman of Dermatology at the University of California, San Diego. His research accomplishments as a physician-scientist include discovery of antimicrobial peptides in mammalian skin, establishing new links between innate immunity and skin diseases such as atopic dermatitis and rosacea, and defining the functions of the skin microbiome in host immune defense.

Brilacidin, an investigational new drug, is a polymer-based antibiotic currently in human clinical trials, and represents a new class of antibiotics called host defense protein mimetics, or HDP-mimetics, which are non-peptide synthetic small molecules modeled after host defense peptides (HDPs). HDPs, also called antimicrobial peptides, some of which are defensins, are part of the innate immune response and are common to most higher forms of life. As brilacidin is modeled after a defensin, it is also called a defensin mimetic.

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

Hemolin is an immunoglobulin-like protein exclusively found in Lepidoptera. It was first discovered in immune-challenged pupae of Hyalophora cecropia and Manduca sexta.

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

Attacin is a glycine-rich protein of about 20 kDa belonging to the group of antimicrobial peptides (AMP). It is active against Gram-negative bacteria.

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

Drosomycin is an antifungal peptide from Drosophila melanogaster and was the first antifungal peptide isolated from insects. Drosomycin is induced by infection by the Toll signalling pathway, while expression in surface epithelia like the respiratory tract is instead controlled by the immune deficiency pathway (Imd). This means that drosomycin, alongside other antimicrobial peptides (AMPs) such as cecropins, diptericin, drosocin, metchnikowin and attacin, serves as a first line defence upon septic injury. However drosomycin is also expressed constitutively to a lesser extent in different tissues and throughout development.

<span class="mw-page-title-main">Dan Hultmark</span> Swedish biologist

Dan Hultmark is a Swedish biologist currently Professor Emeritus, whose research focused on the mechanisms of innate immunity, using Drosophila as a model system, at Umeå University and an Elected Fellow of the American Association for the Advancement of Science. Hultmark is also a member of the Drosophila 12 Genomes Consortium, Tribolium Genome Sequencing Consortium.

<span class="mw-page-title-main">Robert E. W. Hancock</span>

Robert Ernest William Hancock is a Canadian microbiologist and University of British Columbia Killam Professor of Microbiology and Immunology, an Associate Faculty Member of the Wellcome Trust Sanger Institute, and a Canada Research Chair in Health and Genomics.

<i>Drosophila neotestacea</i> Species of fly

Drosophila neotestacea is a member of the testacea species group of Drosophila. Testacea species are specialist fruit flies that breed on the fruiting bodies of mushrooms. These flies will choose to breed on psychoactive mushrooms such as the Fly Agaric Amanita muscaria. Drosophila neotestacea can be found in temperate regions of North America, ranging from the north eastern United States to western Canada.

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

Diptericin is a 9 kDa antimicrobial peptide (AMP) of flies first isolated from the blowfly Phormia terranova. It is primarily active against Gram-negative bacteria, disrupting bacterial membrane integrity. The structure of this protein includes a proline-rich domain with similarities to the AMPs drosocin, pyrrhocoricin, and abaecin, and a glycine-rich domain with similarity to attacin. Diptericin is an iconic readout of immune system activity in flies, used ubiquitously in studies of Drosophila immunity. Diptericin is named after the insect order Diptera.

<span class="mw-page-title-main">Drosocin</span> Antimicrobial peptide

Drosocin is a 19-residue long antimicrobial peptide (AMP) of flies first isolated in the fruit fly Drosophila melanogaster, and later shown to be conserved throughout the genus Drosophila. Drosocin is regulated by the NF-κB Imd signalling pathway in the fly.

<span class="mw-page-title-main">Imd pathway</span> Immune signaling pathway of insects

The Imd pathway is a broadly-conserved NF-κB immune signalling pathway of insects and some arthropods that regulates a potent antibacterial defence response. The pathway is named after the discovery of a mutation causing severe immune deficiency. The Imd pathway was first discovered in 1995 using Drosophila fruit flies by Bruno Lemaitre and colleagues, who also later discovered that the Drosophila Toll gene regulated defence against Gram-positive bacteria and fungi. Together the Toll and Imd pathways have formed a paradigm of insect immune signalling; as of September 2, 2019, these two landmark discovery papers have been cited collectively over 5000 times since publication on Google Scholar.

<span class="mw-page-title-main">Bomanin</span> Antimicrobial peptide-like immune gene of fruit flies

The Bomanin gene family encodes a group of immune peptides that are essential for Drosophila fruit fly defence against infection by many pathogens.

References

  1. Umeå professor linked to Nobel Prize winning research. https://www.umu.se/en/news/umea-professor-linked-to-nobel-prize-winning-research_5832655/
  2. Pütsep, Katrin; Carlsson, Göran; Boman, Hans G.; Andersson, Mats (2002). "Deficiency of antibacterial peptides in patients with morbus Kostmann: An observation study". The Lancet. 360 (9340): 1144–1149. doi:10.1016/S0140-6736(02)11201-3. PMID   12387964. S2CID   40904911.
  3. Faye, Ingrid; Lindberg, Bo G. (2016). "Towards a paradigm shift in innate immunity—seminal work by Hans G. Boman and co-workers". Philosophical Transactions of the Royal Society B: Biological Sciences. 371 (1695): 20150303. doi:10.1098/rstb.2015.0303. PMC   4874399 . PMID   27160604.
  4. Steiner, H.; Hultmark, D.; Engström, Å.; Bennich, H.; Boman, H. G. (1981). "Sequence and specificity of two antibacterial proteins involved in insect immunity". Nature. 292 (5820): 246–248. Bibcode:1981Natur.292..246S. doi:10.1038/292246a0. PMID   7019715. S2CID   4269791.
  5. "The Nobel Prize in Physiology or Medicine 2011".
  6. Pütsep, K.; Faye, I. (2009). "Hans G Boman (1924-2008): Pioneer in Peptide-Mediated Innate Immune Defence". Scandinavian Journal of Immunology. 70 (3): 317–319. doi:10.1111/j.1365-3083.2009.02293.x. PMID   19703022.
  7. "Minisymposium to honour Hans G. Boman - Department of Molecular Biosciences, the Wenner-Gren Institute".
  8. Clemmons, Alexa W.; Lindsay, Scott A.; Wasserman, Steven A. (2015). "An Effector Peptide Family Required for Drosophila Toll-Mediated Immunity". PLOS Pathogens. 11 (4): e1004876. doi: 10.1371/journal.ppat.1004876 . PMC   4411088 . PMID   25915418.