Role of Lipids in Morphogenesis of T-Cell Microvilli
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F21%3A00541309" target="_blank" >RIV/61388955:_____/21:00541309 - isvavai.cz</a>
Result on the web
<a href="http://hdl.handle.net/11104/0318885" target="_blank" >http://hdl.handle.net/11104/0318885</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fimmu.2021.613591" target="_blank" >10.3389/fimmu.2021.613591</a>
Alternative languages
Result language
angličtina
Original language name
Role of Lipids in Morphogenesis of T-Cell Microvilli
Original language description
T cells communicate with the environment via surface receptors. Cooperation of surface receptors regulates T-cell responses to diverse stimuli. Recently, finger-like membrane protrusions, microvilli, have been demonstrated to play a role in the organization of receptors and, hence, T-cell activation. However, little is known about the morphogenesis of dynamic microvilli, especially in the cells of immune system. In this review, I focus on the potential role of lipids and lipid domains in morphogenesis of microvilli. Discussed is the option that clustering of sphingolipids with phosphoinositides at the plasma membrane results in dimpling (curved) domains. Such domains can attract phosphoinositide-binding proteins and stimulate actin cytoskeleton reorganization. This process triggers cortical actin opening and bundling of actin fibres to support the growing of microvilli. Critical regulators of microvilli morphogenesis in T cells are unknown. At the end, I suggest several candidates with a potential to organize proteins and lipids in these structures.
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
10601 - Cell biology
Result continuities
Project
<a href="/en/project/GA19-07043S" target="_blank" >GA19-07043S: Topological regulation of CD4 and CD8 in T cells</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Frontiers in Immunology
ISSN
1664-3224
e-ISSN
1664-3224
Volume of the periodical
12
Issue of the periodical within the volume
MAR 2021
Country of publishing house
CH - SWITZERLAND
Number of pages
7
Pages from-to
613591
UT code for WoS article
000631856900001
EID of the result in the Scopus database
2-s2.0-85103068254