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Leptin affects filopodia and cofilin in NK-92 cells in a dose- and time-dependent manner
Author(s) -
Jana Oswald,
Maximilian Büttner,
Simon JasinskiBergner,
Roland Jacobs,
Philip Rosenstock,
Heike Kielstein
Publication year - 2018
Publication title -
european journal of histochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 42
eISSN - 2038-8306
pISSN - 1121-760X
DOI - 10.4081/ejh.2018.2848
Subject(s) - cofilin , filopodia , leptin , microbiology and biotechnology , immune system , chemistry , adipokine , actin , biology , endocrinology , immunology , cell , actin cytoskeleton , cytoskeleton , biochemistry , obesity
Hyperleptinemia, associated with obesity, is related with immune dysfunction and carcinogenesis. Natural Killer (NK) cells, a major component of the innate immune system are mediators of anti-tumor immunity and the most actively migrating cells among leukocytes. Actin rearrangement, promoted by cofilin plays a central role in cellular migration. Leptin affects the phosphorylation-dependent activity of cofilin and thus actin remodeling. We used human NK-92 cells to explore the in vitro effects of leptin on co-localization of cofilin and F-actin and on morphological changes in NK cells. NK-92 cells were incubated with different leptin concentrations (10 and 100 ng/mL) for 30 min and 24 h and immunocytochemically stained. Results demonstrate a dose- and time-dependent influence of leptin on cellular morphology. Utilizing confocal microscopy, we observed that the co-localization of cofilin-1 and F-actin was slightly influenced by leptin. In summary, the present study demonstrates an impact of a physiological leptin stimulation on the filopodia length, and a time-dependent effect on the co-localization of cofilin and F-actin in NK-92 cells.

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