2003
DOI: 10.1016/s0022-1910(03)00168-9
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Detecting freeze injury and seasonal cold-hardening of cells and tissues in the gall fly larvae, Eurosta solidaginis (Diptera: Tephritidae) using fluorescent vital dyes

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Cited by 71 publications
(68 citation statements)
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“…As hypothesized, we found that cold acclimation also improved cellular survival, as muscle cells from coldacclimated animals had sustained less tissue damage after ≥24 h of cold stress. This observation is consistent with earlier work by Yi and Lee (2003), who found that seasonal cold acclimation and rapid cold hardening improved cellular survival in the freeze-tolerant gall fly larvae Eurosta solidaginis. A similar trend has been observed in the flesh fly Sarcophaga crassipalpis (Yi and Lee, 2004;Teets et al, 2013).…”
Section: Discussion Cold Acclimation Improves Organismal and Cellularsupporting
confidence: 93%
“…As hypothesized, we found that cold acclimation also improved cellular survival, as muscle cells from coldacclimated animals had sustained less tissue damage after ≥24 h of cold stress. This observation is consistent with earlier work by Yi and Lee (2003), who found that seasonal cold acclimation and rapid cold hardening improved cellular survival in the freeze-tolerant gall fly larvae Eurosta solidaginis. A similar trend has been observed in the flesh fly Sarcophaga crassipalpis (Yi and Lee, 2004;Teets et al, 2013).…”
Section: Discussion Cold Acclimation Improves Organismal and Cellularsupporting
confidence: 93%
“…In our study, we did not observe changes of actin within the Malpighian tubules, ovaries, or thoracic muscles; only the midgut displayed obvious actin changes in response to low temperature. Specific tissues in different species and different developmental stages have their own distinct responses related to survival at high or low temperature (Krebs and Feder, 1997;Yi and Lee, 2003;Lee et al, 2006), and it appears that the midgut is one of the tissues most responsive to low temperature in Cx. pipiens..…”
Section: Discussionmentioning
confidence: 99%
“…Following a 24h recovery from exposure to -18°C, midguts were dissected from living, non-moribund larvae in Coast's solution (Coast and Krasnoff, 1988). Tissue samples were stained using the The Journal of Experimental Biology 216 (20) THE JOURNAL OF EXPERIMENTAL BIOLOGY LIVE/DEAD sperm viability kit, as described previously (Yi and Lee, 2003), and images were documented using fluorescent microscopy. With this staining technique, living cells with intact membranes fluoresced green, whereas dead cells with damaged membranes fluoresced red.…”
Section: Assessment Of Cell Survival Of Midgut Tissuementioning
confidence: 99%