The structure and function of Iristatin, a novel immunosuppressive tick salivary cystatin
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12310%2F19%3A43899427" target="_blank" >RIV/60076658:12310/19:43899427 - isvavai.cz</a>
Alternative codes found
RIV/60077344:_____/19:00519639 RIV/61388963:_____/19:00519639
Result on the web
<a href="https://link.springer.com/content/pdf/10.1007%2Fs00018-019-03034-3.pdf" target="_blank" >https://link.springer.com/content/pdf/10.1007%2Fs00018-019-03034-3.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00018-019-03034-3" target="_blank" >10.1007/s00018-019-03034-3</a>
Alternative languages
Result language
angličtina
Original language name
The structure and function of Iristatin, a novel immunosuppressive tick salivary cystatin
Original language description
To successfully feed, ticks inject pharmacoactive molecules into the vertebrate host including cystatin cysteine protease inhibitors. However, the molecular and cellular events modulated by tick saliva remain largely unknown. Here, we describe and characterize a novel immunomodulatory cystatin, Iristatin, which is upregulated in the salivary glands of feeding Ixodes ricinus ticks. We present the crystal structure of Iristatin at 1.76 angstrom resolution. Purified recombinant Iristatin inhibited the proteolytic activity of cathepsins L and C and diminished IL-2, IL-4, IL-9, and IFN- production by different T-cell populations, IL-6 and IL-9 production by mast cells, and nitric oxide production by macrophages. Furthermore, Iristatin inhibited OVA antigen-induced CD4(+) T-cell proliferation and leukocyte recruitment in vivo and in vitro. Our results indicate that Iristatin affects wide range of anti-tick immune responses in the vertebrate host and may be exploitable as an immunotherapeutic.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cellular and Molecular Life Science
ISSN
1420-682X
e-ISSN
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Volume of the periodical
76
Issue of the periodical within the volume
10
Country of publishing house
CH - SWITZERLAND
Number of pages
11
Pages from-to
2003-2013
UT code for WoS article
000465438900011
EID of the result in the Scopus database
2-s2.0-85061431964