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Mating in Dolly Vardens (Salvelinus malma) was studied in relation to individuals' dominance ranks in a landlocked population in south-central Alaska. Two types of
tactics were adopted by males: pairing directly with a spawning female and streaking to a spawning pair. Average success in
sperm release was 97% in pairing but only 47% in streaking, and depended on the distance to the female. The pairing tactic
was mostly monopolized by males of primary and secondary dominance rank. These dominant males were the largest (≥210 mm in
fork length) and the oldest (≥6 years) individuals. Their mating success per season was much higher than that of the smaller
and younger males. 相似文献
404.
Hideki Tanaka Hirotsugu Hino Shota Moriya Hiromi Kazama Masaya Miyazaki Naoharu Takano Masaki Hiramoto Kiyoaki Tsukahara Keisuke Miyazawa 《Biochemistry and Biophysics Reports》2020
Tyrosine kinase inhibitors (TKIs) induce autophagy in many types of cancer cells. We previously reported that gefitinib (GEF) and imatinib (IMA) induce autophagy in epidermal growth factor receptor (EGFR) knock-out A549 and non-BCR-ABL-expressing leukemia cell lines, respectively. This evidence suggests that TKI-induced autophagy is independent of the original target molecules. The present study compared the autophagy-inducing abilities of various TKIs, regardless of their targets, by quantitative autophagy flux assay. We established stable clones expressing the GFP-LC3-mCherry-LC3ΔG plasmid in A549, PC-9, and CAL 27 cell lines and assessed autophagy inducibility by monitoring the fluorescent ratios of GFP-LC3 to mCherry-LC3ΔG using an IncuCyte live cell imaging system during exposure to TKIs viz; GEF, osimertinib (OSI), lapatinib (LAP), lenvatinib (LEN), sorafenib (SOR), IMA, dasatinib (DAS), and tivantinib (TIV). Among these TKIs, DAS, GEF, and SOR exhibited prominent autophagy induction in A549 and PC-9 cells. In CAL 27 cells, IMA, SOR, and LEN, but not GEF, TIV, or OSI, exhibited autophagy induction. In the presence of azithromycin (AZM), which showed an inhibitory effect on autophagy flux, TKIs with prominent autophagy inducibility exhibited enhanced cytotoxicity via non-apoptotic cell death relative to effects of TKI alone. Therefore, autophagy inducibility of TKIs differed in the context of cancer cells. However, once induced, they appeared to have cytoprotective functions. Thus, blocking TKI-induced autophagy with AZM may improve the therapeutic effect of TKIs in cancer cells. 相似文献