The heat shock response of cells is thought to have a role in ameliorating cellular damage and preventing programmed cell death in thermal and other stress environments.1 The protective effects of heat shock proteins (Hsps) are likely mediated by the ability of these proteins to function as molecular chaperones, preventing inappropriate protein aggregation and facilitating transport of immature proteins to target organelles for packing, degradation, or repair. Increased expression of Hsp70 in response to temperature slightly above physiological temperatures (e.g., ), for periods of several minutes has been studied as a potential treatment for indications such as ischemic heart disease, diabetes, neurodegeneration, cancer, and thermal damage.1, 2 Hsp70 expression can be induced at the level of transcription in all cell and tissue types that have been examined, and significant intraspecies sequence similarity suggests that it has been conserved through evolution.
Ablation techniques that employ lasers for tissue removal or remodeling can result in very high temperatures for extremely short periods of time, and levels of Hsp expression in adjacent tissues may correlate with healing or may predict the extent of tissue damage. Previous studies have shown that Hsps serve as strong predictors for cancer cell survival and resistance following laser cancer therapy.1, 3 Understanding the patterns of Hsp transcription in tissues surrounding ablation sites will reveal the nature of the accompanying stress and may aid in the development of more effective tissue ablation and regeneration strategies. Ferrando first showed induction of Hsp70 in cells using a laser with a one second pulse duration.4 Others have quantified the expression of Hsp70 using bioluminescent reporters in cells and “raft cultures,” a surrogate tissue model,5, 6, 7 after exposure to thermal stresses.
The effects of high temperature exposure for extremely short durations during irradiation may differ significantly given that the shock is determined by the time of energy deposition (e.g., laser pulse duration), and the heat dissipation time (thermal diffusion time), which can greatly exceed the energy deposition time. In situations where the energy deposition time is less than the thermal confinement time (the time associated with heat remaining in a specific region), there is no diffusion and thus the peak temperatures can be much higher than where thermal diffusion takes place. Taking a typical value of heat conductivity for biological tissue of and cell size of , the heat dissipation time from a single cell within living tissue is on the order of .
To refine the laser parameters (wavelength, spotsize, pulse duration, radiant exposure) appropriate for laser surgery and tissue remodeling as well as diagnostic laser applications, it is important to understand the spatial and temporal patterns of cellular responses to thermal insults up to and including the threshold for irreversible cellular damage or ablation in these short, high temperature pulses.
In a previous study,5 we generated an Hsp70-luc reporter gene and used it to study Hsp70 expression patterns in stable lines of NIH3T3 fibroblast cells to determine the dynamic response of Hsp70 expression. Transfected cells were first treated at in a water bath for durations of and luciferase expression was monitored at 2, 10, and 24 h.5 Shorter exposures to higher temperatures were studied from for exposure times of using a thermocycler.5 In this and other studies,5, 6 cells treated with the shorter duration thermal stress (several seconds) were found to survive relatively high temperatures ; however, extremely short durations, corresponding to thermal confinement times (on the order of microseconds) were not evaluated.
Transgenic (Tg) mice, with the Hsp70 promoter and a reporter gene, have been used in analysis of thermal stress.8 To facilitate analysis of thermal stresses at very short pulse durations, we have developed a Tg mouse based on a modified reporter, construct that employs the Hsp70A1 promoter and a dual reporter, comprised of firefly luciferase and enhanced green fluorescent protein (eGFP) joined by the 2A “ribosome slippage site” from the foot and mouth disease virus (Hsp70A1-luc-2A-GFP).5, 6, 9 This dual reporter construct allows for the macroscopic analysis of Hsp70 expression in skin in vivo via luciferase expression using BLI. We used this Tg mouse to assess laser thermal stress and the resultant spatiotemporal patterns of Hsp70 expression in the skin in vivo after irradiation.
Transgenic Reporter Mouse
The Hsp70-luc reporter was described previously, and shown to accurately report levels of Hsp70 transcription in cell lines.5 To increase the functional capability of this reporter construct, the gene coding for enhanced green fluorescent protein (eGFP, Clontech, Palo Alto, California) was added. For this, we employed the dual reporter gene L2G (Luc-2A-eGFP) consisting of a modified firefly luciferase gene (pGL3, Promega Incorporated, Madison, Wisconsin) joined to 54 base pairs (bp) of the FMDV 2A sequence9 and, via of polylinker sequence, to the eGFP gene at the end. Using the restriction enzyme sites Hind III and Not I, the L2G gene was inserted into the vector pcDNA3.1(-) (Invitrogen, Carlsbad, California), in which the CMV promoter had been replaced by the Hsp70A1 promoter.5 Finally, the Hsp70-L2G reporter gene fragment was excised from the vector backbone and gel purified for pronuclear injection. Microinjection was performed by the Transgenic Core Facility in the Department of Pathology at Stanford University using preimplantation embryos derived from FVB mice. Potential founders were screened by polymerase chain reaction and tested for thermal response by exposure to mild thermal stress and BLI using an IVIS imaging system (Xenogen, Alameda, California). The selected Tg mouse line (FVB.Hsp70-luc-2A-eGFP; short form—Hsp70A1-L2G) was bred to homozygosity, and four to eight week old female mice were used for the in vivo experiments.
Laser Thermal Stress Analysis
Tissue thermal stress was generated with a laser (PLX-100, Parallax Technology Incorporated, Waltham, Massachusetts) and evaluated in the Hsp70A1-L2G mouse. Using the laser, the dorsal skin of the transgenic mice was irradiated at a wavelength of . Mice were shaved and depilated prior to irradiation with the laser— was sufficient time to prevent residual expression of Hsp70 caused by shaving. Experiments were performed with a pulse duration. Four irradiation spots were generated at separate locations on the back of each mouse in a grid pattern at 1.8, 2.7, 3.5, and [Fig. 1a ]. A -diam flat-top spot, created by irradiating the mouse with the central part of a Gaussian beam with a hole drilled through an aluminum plate, was used to generate an affected area large enough to provide adequate resolution to determine the expression profile using an IVIS 200 imaging system (Xenogen/Caliper Life Sciences), with high resolution binning (4) and a field of view to obtain a resolution across each treated location. BLI was performed postintraperitoneal (IP) injection of mouse of stock solution of D-luciferin (Biosynth L-8220, Staad, Switzerland) with a integration time.
BLI was used to analyze the approximate levels of Hsp70 transcriptional activation following laser injury to the skin. This approach enabled macroscopic analysis of individual lesions in live mice with temporal resolution that is relevant to Hsp70 induction [Fig. 1a]. The short half life of the luciferase enzyme ( 10) results in the assay being one of transcriptional activity,5 and as such both the activation and cessation of transcription can be assessed.5 The levels of Hsp70 and luciferase will differ with protein stability, and the half life of luciferase enzyme results in a dynamic assay.5, 6 Figure 1 reveals the temporal responses of the heat shock reporter to irradiation of skin with a laser. Profile plots of each lesion generated by the laser were obtained at five imaging times for comparison [Fig. 1b] by placing a line across the center of each lesion using ImageJ (National Institutes of Health, Washington, DC) and examining the profile of expression across this line. The profile plots are from the same images used in Fig. 1a. The peak radiance was obtained by placing a region of interest (ROI) with a -diam around each irradiated spot of each mouse image and measuring the peak radiance using Living Image Software (Xenogen/Caliper, Hopkinton, Massachusetts), Fig. 1d.
Discussion and Conclusions
Analysis shows a qualitative peak of expression at postirradiation, which is apparent up to . Intermediate energy levels caused reduced expression. The results are displayed as a linear profile plots across the center of each lesion. Highest radiant exposure images show a ring-like expression contour surrounding an inner region of reduced expression. This expression contour is seen as two distinct peaks at either edge of the lesion in the profile plots. Since luciferase activity is dependent on the metabolic activity of the cell, reporter activity is lost at the time of cell death and the patterns of expression are consistent with this link to cell viability. Intermediate energy levels produced a Gaussian profile similar to those obtained for the lowest radiant exposures. Antibody staining of GFP in tissue sections from samples subjected to similar laser parameters have indicated that GFP and Hsp70 expression correlate spatially throughout the laser spot (data not shown).
In this study, we demonstrate the creation and validation of a transgenic mouse that enables the rapid analysis of cellular injury and survival in response to laser tissue injury. This Hsp70 reporter mouse model will serve as an excellent indicator of cellular stress, cell survival, collateral damage, and wound healing in vivo.
This work was funded by a grant from the Air Force Office of Scientific Research (F49620-00-1-0349). Contag is a consultant for Caliper Life Sciences, Hopkinton, Massachusetts.
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