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Lifetime Calling Patterns and Tactics in the Field Cricket Teleogryllus emma (Orthoptera: Gryllidae)
Soojin Jang,Yikweon Jang,Jae Chun Choe 한국응용곤충학회 2009 한국응용곤충학회 학술대회논문집 Vol.2009 No.05
Males of many cricket species produce calling songs to attract receptive, conspecific females. Calling songs which affected by calling pattern are critical for male mating success, since male with no or limited calling songs are unable to attract female crickets. Investigating among- and within-individual variation in calling pattern may reveal the presence of alternative mating tactics such as attracting females by producing calling songs or being satellites in which males intercept females who are attracted to calling males. In this study, I investigated patterns of calling song production during the entire adulthood of 32 laboratory-reared and 24 field-captured individuals of Teleogryllu emma. Using recording system which can record acoustic signals from up to 32 individuals simultaneously, I measured daily calling output (DCO) and total calling output (TCO) in addition to acoustic parameters of calling songs and classified T.emma males into consistent and inconsistent singers based on the consistency of singing. Consistent singers lived longer, sang longer both in a day and during the lifetime than the inconsistent singers. These results suggest that the consistent singers in this study may be considered to employ the calling tactic. In lab-reared individuals, there seemed to be a trade-off between increasing pulse duration and length of phrases and ling chirp although older males produced calling songs with longer ling chirps and more multiple phrases.
No Effect of the Acoustic Stimulus on the Reproductive Rate in Myzus persicae
Soojin Jang,Yikweon Jang 한국응용곤충학회 2012 한국응용곤충학회 학술대회논문집 Vol.2012 No.10
An aphid usually stays at one feeding site for a long time for development and reproduction. The green peach aphids, Myzus persicae (Sulzer), feed consistently and regularly throughout all stages of nymphs and adult at one feeding site. In M. persicae, honey dew production, which indicates a state of feeding, occurs at regular intervals within a given stage, and moving, which may be related to escape or dispersal, interrupts feeding, The results of the playback experiments showed that acoustic stimuli with frequencies of 100 and 10000 Hz were effective in inducing feeding repression in M. persicae. That is, HDP occurred less often, and MV occurred more often and longer under acoustic stimuli. In this study, we tested whether the acoustic stimulus effective for inducing feeding suppression decreased reproductive rate in M. persicae. A group of 20 aphids were placed in a host plant and was subject to the acoustic stimulus with two frequency components, 100 and 10000 Hz, for a given time (1, 3, 6, and 12 hours) each day for four days. The result of this experiment showed that the acoustic stimulus did not affect the reproductive rate, regardless of exposure time, in M. persicae.
Jang, Soojin,Ryu, Se Min,Lee, Jooyeon,Lee, Hanbyeol,Hong, Seok-Ho,Ha, Kwon-Soo,Park, Won Sun,Han, Eun-Taek,Yang, Se-Ran The Korean Academy of Tuberculosis and Respiratory 2019 Tuberculosis and Respiratory Diseases Vol.82 No.2
Background: Idiopathic pulmonary fibrosis involves irreversible alveolar destruction. Although alveolar epithelial type II cells are key functional participants within the lung parenchyma, how epithelial cells are affected upon bleomycin (BLM) exposure remains unknown. In this study, we determined whether BLM could induce cell cycle arrest via regulation of Schlafen (SLFN) family genes, a group of cell cycle regulators known to mediate growth-inhibitory responses and apoptosis in alveolar epithelial type II cells. Methods: Mouse AE II cell line MLE-12 were exposed to $1-10{\mu}g/mL$ BLM and $0.01-100{\mu}M$ baicalein (Bai), a G1/G2 cell cycle inhibitor, for 24 hours. Cell viability and levels of pro-inflammatory cytokines were analyzed by MTT and enzyme-linked immunosorbent assay, respectively. Apoptosis-related gene expression was evaluated by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR). Cellular morphology was determined after DAPI and Hoechst 33258 staining. To verify cell cycle arrest, propidium iodide (PI) staining was performed for MLE-12 after exposure to BLM. Results: BLM decreased the proliferation of MLE-12 cells. However, it significantly increased expression levels of interleukin 6, tumor necrosis factor ${\alpha}$, and transforming growth factor ${\beta}1$. Based on Hoechst 33258 staining, BLM induced condensation of nuclear and fragmentation. Based on DAPI and PI staining, BLM significantly increased the size of nuclei and induced G2/M phase cell cycle arrest. Results of qRT-PCR analysis revealed that BLM increased mRNA levels of BAX but decreased those of Bcl2. In addition, BLM/Bai increased mRNA levels of p53, p21, SLFN1, 2, 4 of Schlafen family. Conclusion: BLM exposure affects pulmonary epithelial type II cells, resulting in decreased proliferation possibly through apoptotic and cell cycle arrest associated signaling.
( Soojin Jang ),( Se Min Ryu ),( Jooyeon Lee ),( Hanbyeol Lee ),( Seok-ho Hong ),( Kwon-soo Ha ),( Won Sun Park ),( Eun-taek Han ),( Se-ran Yang ) 대한결핵 및 호흡기학회 2019 Tuberculosis and Respiratory Diseases Vol.82 No.2
Background: Idiopathic pulmonary fibrosis involves irreversible alveolar destruction. Although alveolar epithelial type II cells are key functional participants within the lung parenchyma, how epithelial cells are affected upon bleomycin (BLM) exposure remains unknown. In this study, we determined whether BLM could induce cell cycle arrest via regulation of Schlafen (SLFN) family genes, a group of cell cycle regulators known to mediate growth-inhibitory responses and apoptosis in alveolar epithelial type II cells. Methods: Mouse AE II cell line MLE-12 were exposed to 1-10 μg/mL BLM and 0.01-100 μM baicalein (Bai), a G1/G2 cell cycle inhibitor, for 24 hours. Cell viability and levels of pro-inflammatory cytokines were analyzed by MTT and enzymelinked immunosorbent assay, respectively. Apoptosis-related gene expression was evaluated by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR). Cellular morphology was determined after DAPI and Hoechst 33258 staining. To verify cell cycle arrest, propidium iodide (PI) staining was performed for MLE-12 after exposure to BLM. Results: BLM decreased the proliferation of MLE-12 cells. However, it significantly increased expression levels of interleukin 6, tumor necrosis factor α, and transforming growth factor β1. Based on Hoechst 33258 staining, BLM induced condensation of nuclear and fragmentation. Based on DAPI and PI staining, BLM significantly increased the size of nuclei and induced G2/M phase cell cycle arrest. Results of qRT-PCR analysis revealed that BLM increased mRNA levels of BAX but decreased those of Bcl2. In addition, BLM/Bai increased mRNA levels of p53, p21, SLFN1, 2, 4 of Schlafen family. Conclusion: BLM exposure affects pulmonary epithelial type II cells, resulting in decreased proliferation possibly through apoptotic and cell cycle arrest associated signaling.