Naslov
Maturation of Monocyte-Derived DCs Leads to Increased Cellular Stiffness, Higher Membrane Fluidity, and Changed Lipid Composition

Autori
Lühr, Jennifer J. ; Alex, Nils ; Amon, Lukas ; Kräter, Martin ; Kubánková, Markéta ; Sezgin, Erdinc ; Lehmann, Christian H. K. ; Heger, Lukas ; Heidkamp, Gordon F. ; Smith, Ana- Sunčana ; Zaburdaev, Vasily ; Böckmann, Rainer A. ; Levental, Ilya ; Dustin, Michael L. ; Eggeling, Christian ; Guck, Jochen ; Dudziak, Diana

Izvornik
Frontiers in Immunology (1664-3224) 11 (2020); 590121, 18

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
cell mechanics, cellular stiffness, lipids, lipidomics, monocyte-derived dendritic cells, maturation, lowdensity lipoprotein, cholesterol
(cell mechanics, cellular stiffness, lipids, lipidomics, monocyte-derived dendritic cells, maturation, low density lipoprotein, cholesterol)

Sažetak
Dendritic cells (DCs) are professional antigen- presenting cells of the immune system. Upon sensing pathogenic material in their environment, DCs start to mature, which includes cellular processes, such as antigen uptake, processing and presentation, as well as upregulation of costimulatory molecules and cytokine secretion. During maturation, DCs detach from peripheral tissues, migrate to the nearest lymph node, and find their way into the correct position in the net of the lymph node microenvironment to meet and interact with the respective T cells. We hypothesize that the maturation of DCs is well prepared and optimized leading to processes that alter various cellular characteristics from mechanics and metabolism to membrane properties. Here, we investigated the mechanical properties of monocyte-derived dendritic cells (moDCs) using real-time deformability cytometry to measure cytoskeletal changes and found that mature moDCs were stiffer compared to immature moDCs. These cellular changes likely play an important role in the processes of cell migration and T cell activation. As lipids constitute the building blocks of the plasma membrane, which, during maturation, need to adapt to the environment for migration and DC-T cell interaction, we performed an unbiased high- throughput lipidomics screening to identify the lipidome of moDCs. These analyses revealed that the overall lipid composition was significantly changed during moDC maturation, even implying an increase of storage lipids and differences of the relative abundance of membrane lipids upon maturation. Further, metadata analyses demonstrated that lipid changes were associated with the serum low-density lipoprotein (LDL) and cholesterol levels in the blood of the donors. Finally, using lipid packing imaging we found that the membrane of mature moDCs revealed a higher fluidity compared to immature moDCs. This comprehensive and quantitative characterization of maturation associated changes in moDCs sets the stage for improving their use in clinical application.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Interdisciplinarne prirodne znanosti, Interdisciplinarne biotehničke znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)

Napomena
This work was partly supported by grants from
the German Research Foundation [Deutsche
Forschungsgemeinschaft (DFG)] to DD (CRC1181-
TPA7, DU548/5-1), to DD, RB, and A-SS
(RTG1962); the Emerging Fields Initiative BIG-
THERA of the Friedrich-Alexander University
Erlangen-Nürnberg to DD and A-SS; Erlanger
Leistungsbezogene Anschubfinanzierung und
Nachwuchsförderung (ELAN) (DE-17-09-15-1-Heger)
to LH; Interdisziplinäres Zentrum für Klinische
Forschung (IZKF) (IZKF-A80) to DD; Wellcome and
Kennedy Trust for Rheumatology Research (PRF
100262Z/12/Z) to MD. ES is supported by
SciLifeLab fellow program. CE acknowledges
imaging support by the Wolfson Imaging Centre –
Oxford, and funding by the Wolfson Foundation,
the EPA Cephalosporin Fund, MRC (Grant No.
MC_UU_12010/unit programs G0902418 and
MC_UU_12025), the Wellcome Trust (Grant No.
104924/14/Z/14 and Strategic Award 091911
(Micron)), MRC/BBSRC/EPSRC (Grant No.
MR/K01577X/1), the John Fell Fund, state of
Thuringia (Thüringer Aufbaubank (TAB)), the
Deutsche Forschungsgemeinschaft (Research unit
1905, Jena Excellence Cluster “Balance of the
Microverse” and Collaborative Research Center
1278) and the Jena Center of Soft Matter.

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