Lung cancer is the deadliest malignancy in the US and worldwide.1 Despite advances in medical imaging, the five-year survival rate has remained low because most lung cancer cases are presently diagnosed at locally advanced or metastatic stages of disease.1 Clinical studies have recently shown that screening asymptomatic smokers for lung cancer leads to detecting tumors at an earlier and therefore more curable stage of disease.2,3 Although improvements in medical imaging allow detection of smaller nodules, direct and minimally invasive diagnosis of these nodules could reduce the number of unnecessary biopsies and follow-up procedures. This suggested the need for new imaging approaches that provide high-resolution interrogation in real-time and accurately distinguish malignant nodules from other disease states. Here, we evaluate the applicability of multiphoton microscopy (MPM) for visualizing lung disease by determining the two-photon excited endogenous fluorescence and second harmonic generation (SHG) of ex vivo lung using mouse models of lung cancer and by suggesting potential MPM detected criteria for the classification of lung lesions.
A variety of optical imaging modalities have been implemented as endoscopic devices for in vivo detection of neoplasias in internal organs.45.6.–7 In the lungs, wide-field autofluorescence bronchoscopes have already been tested clinically for the detection of early bronchial tumors,8 and confocal microendoscopes have been applied for the in vivo imaging of alveolar ducts.9 Here, we introduce MPM as a potential imaging modality for diagnostic visualization of lung neoplasms.
MPM is one of the preferred microscopy modalities for subcellular resolution imaging of optically scattering tissue due to the deeper penetration depth and the minimized photodamage of the near-infrared excitation light.1011.–12 Intrinsic two-photon excited fluorescence and SHG from tissue provide subcellular resolution images with sufficient morphological details to be diagnostically useful, as has been demonstrated with unprocessed biopsies from human urinary bladder,13 ovary,14 gastrointestinal tract,15 and prostate samples.16 Similar to the established diagnostic methods of histopathology, the endogenous fluorescence and SHG captured by MPM images provide information about the tissue architecture of the interrogated site. MPM also allows the visualization of intrinsic fluorescence patterns on a cellular level and changes in fluorescence emission as tissues develop abnormalities. Common cellular fluorophores in unprocessed tissue include intrinsic metabolic indicators such as NADH and flavins.12,17,18 Extracellular endogenous signals in MPM images originate from structural fibers such as collagen and elastin.12 SHG from collagen is unique to MPM imaging and has been used to monitor changes in collagen composition due to tumor development that were not obvious by standard histopathology.19 Therefore, multiphoton excitation microscopy has the potential to visualize both microanatomical and spectral properties without the need for tissue processing.
The respiratory lung consists of alveolar ducts with numerous alveoli that are lined by a layer of flattened epithelial cells and by a septum with alveolar capillaries, as well as elastin and collagen fibers.20 Previous MPM studies have shown that endogenous signal from normal human21 and mouse22 lung originates predominantly from the alveolar septa of intact alveoli, with collagen fibers emitting SHG at half the excitation wavelength, and elastin fibers having a broad endogenous fluorescence in the green emission region. Lung adenocarcinoma, the most common type of human lung cancer, is believed to form in some cases after progressive pathological changes and to arise from a preinvasive lesion of atypical epithelial cells called atypical adenomatous hyperplasia (AAH).23 In contrast to the normal lung parenchyma, adenocarcinomas are characterized as cellular masses with diverse histopathology that distort the fibrous alveolar network.24
We evaluated the two-photon excited endogenous fluorescence and SHG of unprocessed normal, preneoplastic and neoplastic lung in two different mouse lung cancer models. We imaged unprocessed lungs from a mouse model of lung adenocarcinoma based on the conditional expression of the oncogene K-ras that genetically mimics human lung adenocarcinoma and allows investigation of lesions at well defined and predictable (including early) stages of tumor progression.25 In this model, targeted delivery of Cre recombinase activates the expression of a conditional K-ras allele (LSL-K-ras G12D) in scattered cells throughout the lungs, resulting in precursor lesions, such as AAH, that progress to adenomas and adenocarcinomas in a reproducible, temporal sequence. We also imaged lung from a second mouse model based on transgenic overexpression of Rrm2, a subunit of the enzyme ribonucleotide reductase (RNR) that is a key regulator of de novo nucleotide biosynthesis.26 Tumorigenesis in Rrm2 overexpressing transgenic () mice involves a mutagenic mechanism that recapitulates the stochastic nature of tumor development in humans and results in lesions with histopathological resemblance to human lung neoplasms. Furthermore, we confirmed diverse applicability of our findings in a case of spontaneously occurring canine lung cancer. This proof-of-principle study of mouse and dog lung neoplasms demonstrates the potential of MPM as an imaging technique for lung nodules, and provides clear motivation for MPM applications for in vivo evaluation of lung cancer, particularly by endoscopy.
Materials and Methods
Mouse Models of Lung Adenocarcinoma
LSL-K-ras G12D mice25 were obtained from the Mouse Models of Human Cancer Consortium and backcrossed either onto a pure 129SvEv or onto an FVB/N genetic background. To induce Cre-mediated recombination and K-ras G12D activation in the lungs, adult mice were anesthetized with 2.5% Avertin (tribromoethanol and tert-amyl alcohol) and were administered plaque-forming units (PFU) of Ad-Cre virus, diluted in 40 μl of phosphate buffered saline (PBS), either intratracheally or intranasally. Note that , or dilutions were used for some mice. The lungs were harvested 6 to 20 weeks post infection from euthanized mice. mice were maintained on pure FVB/N genetic background as previously described.26 All animal housing and experimentation was performed in accordance with institutional animal care and use guidelines.
Lung Tissue Processing and Histopathological Assessment
Mice were euthanized by carbon dioxide asphyxiation. The lung lobes were removed and visually inspected for abnormalities. Normal lung has a uniform pink color throughout the surface of the lobes, whereas regions with potential abnormalities appear as white or red discolorations in the smooth surface of the lung. Sites with abnormal appearance were selected on each lobe and imaged within two hours after euthanasia. All lobes were kept in chilled PBS until imaging. Immediately after imaging, the lobes were fixed in 10% buffered formalin or 4% paraformaldehyde. H&E stained sections were prepared from each lobe following standard embedding and staining protocols. H&E sections ( thick) were obtained from a similar depth and location within samples to that imaged by MPM. Low-magnification micrographs were obtained for each H&E section and compared to a low-magnification MPM image of the lobe prior to tissue fixation. Using structural features present on both the H&E and MPM image, the location of the site imaged at high-magnification MPM was approximated on the H&E section. Thus, histopathological assessment was performed at a site on the H&E section comparable to the site imaged with MPM prior to tissue processing. Pathological assessment was performed according to guidelines in the Mouse Models of Human Cancers Consortium.27
Lung samples were also obtained from a 12-year-old female spayed Miniature Poodle treated at the Cornell University Hospital for Animals for bronchioloalveolar carcinoma of the left caudal lung lobe. The left caudal lung lobe was removed by standard lung lobectomy by a veterinary surgeon. Clinically abnormal and normal samples were obtained from the resected lobe by a veterinary oncologist. Prior to surgery, an informed consent form was signed by the owner of the dog. The samples were kept in chilled PBS for about two hours prior to imaging. Similar tissue imaging and processing were followed as for mouse lungs.
MPM of Unprocessed Lung Tissue
Imaging was performed with a commercial multiphoton microscope (Olympus Fluoview® FV1000MPE, Olympus America Inc, Center Valley, PA) at a shorter (760 nm) and longer (860 nm) excitation. An Olympus , 1.05 NA water immersion objective was used and all images were obtained with (at 760 nm excitation) and (at 860 nm excitation) average power at the objective, pixel dwell time of 2 μs and at . Displayed MPM images represent a Kalman average of three frames. Autofluorescence and SHG were captured by three detection channels, equipped with multi-alkali photomultiplier tubes. The first channel detected signal at 420 to 460 nm, the second and third channels captured endogenous fluorescence at 500 to 550 nm and at 575 to 635 nm; respectively. Images from each channel were pseudocolored and superimposed. Displayed MPM images represent superimposed images: “green” pixels indicates fluorescence detected predominantly in the second channel, “red” indicates fluorescence detected predominantly in the third channel and “blue” indicates emission at 420 to 460 nm (including SHG at 860 nm excitation only). The contrast and brightness were adjusted equally for all displayed MPM images at a particular excitation wavelength.
MPM was performed on lobes from eight control mice, including uninfected and Ad-Cre infected wild-type mice, and on lobes from 10 Ad-Cre infected LSL-K-ras G12D mice and two tumor bearing mice. Images were taken from 1 to 4 sites per lobe. Unaffected lobes with normal appearance were imaged approximately 20 to 30 μm below the pleura at a representative site. Lobes with grossly visible abnormalities were imaged at several sites to 30 μm below the pleura; an image was taken from the center of each nodule and the tissue surrounding the nodule. For larger or heterogeneous nodules, images were taken from different areas within the nodule. In total, images were obtained from eleven tumor free unaffected (normal) lung sites, four adenomas, six adenocarcinomas, three sites with focal inflammation and six regions with diffuse hyperplasia. MPM images from adenomas and adenocarcinomas were analyzed by determining the Green (500 to 550 nm)/Blue (420 to 460 nm) fluorescence emission ratio for each MPM image (defined as the average pixel intensity value from the green channel (500 to 550 nm) divided by the sum of the average pixel intensity values from the blue (420 to 460 nm) and green channel (500 to 550 nm). The ratio was calculated only for pixels within the nodule and not from the surrounding tissue.
Two-Photon Excited Microspectroscopy of Unprocessed Lung Tissue
Microspectroscopy was performed using a spectrograph (Andor Technology, South Windsor, CT, USA) coupled to the microscope with a multimode optical fiber. A spectroscopic EEM CCD (Andor Technology, South Windsor, CT, USA), attached to the spectrograph, was used in full vertical binning mode to measure spectra from the imaged sample. Spectra were obtained by scanning a zoomed in () region within each MPM image for an exposure time of 1.18 sec and average power at the objective of (at 760 nm excitation) and (at 860 nm excitation). Spectra were obtained at to 30 μm below the pleura. No photodamage was observed in the zoomed-in regions after spectroscopic acquisition.
Microspectroscopy was performed on lesions with dense cellular aggregations such as adenomas, adenocarcinomas and focal inflammatory sites. During MPM imaging at 760 nm, regions within each tumor composed of cells with dominant fluorescence at 420 to 460 nm were visually selected. Next, three spectra were sampled from zoomed in () areas within these preselected regions. In focal inflammatory sites, clusters of inflammatory cells with yellow appearance on MPM images were sampled. Spectra were also obtained from normal sites by sampling zoomed in regions of the alveolar septa from unaffected alveoli. All spectra were background subtracted, smoothed by a Savitzky-Golay filter (MATLAB), and normalized by the maximum intensity value in the 400 to 650 nm region prior to analysis.
To elucidate the intrinsic fluorescence and SHG patterns of peripheral lung tissue at different pathological stages, we obtained MPM images and two-photon excited fluorescence spectra from tumor-free unaffected, inflammatory and hyperplasic lung sites and from lung tumors, such as adenomas and adenocarcinomas. Images were visually analyzed to suggest a set of structural and spectral features for MPM-guided differentiation of lung sites at different pathological stages.
Two-Photon Excited Intrinsic Fluorescence Features of Tumor Free Peripheral Mouse Lung
To demonstrate the ability of MPM to differentiate normal from diseased lung, ex vivo MPM was first performed on tumor-free unaffected peripheral lung [Figs. 1(a)–1(f)]. MPM images showed similar microanatomical features to histopathology, with intact alveolar spaces and clearly apparent septa. The thin layer of epithelial cells comprising the alveoli was not visualized by MPM, and the two-photon excited intrinsic emission appeared to originate from the alveolar septa, not the associated epithelium. At 760 nm excitation, the brightest fluorescence originated from granular structures; individual cells were not readily visualized. Two-photon excited fluorescence spectra of intact alveoli from eleven different tumor-free unaffected lung sites peaked at (data not shown), which differed from fluorescence of typical cellular fluorophores such as NADH and flavins.12,17,18 At 860 nm excitation, fluorescence originated predominantly from fibers within the alveolar walls that appeared green in MPM images [Fig. 1(c)], indicating fluorescence detected at 500 to 550 nm. Some alveoli also displayed fibers with blue appearance in MPM images [Figs. 1(f) and 2(c)], probably caused by SHG at 430 nm from collagen fibers in the alveolar septa. Microanatomically, this signal correlates well with the collagen distribution in Masson’s trichrome stained tumor-free peripheral lung [Fig. 2(a)], indicating that fibers with blue appearance at 860 nm represent collagen from the alveolar septa. Intact alveoli without a readily visualized cellular component were observed in MPM images from all tumor-free lung sites and used as an MPM-detected feature to differentiate tumor-free and diseased lung in this study (Table 1).
Structural and spectral features observed in multiphoton microscopy (MPM) images of normal, inflammatory and neoplastic lung. The spectral features observed in MPM images were also supported by two-photon excited microspectroscopy. While standard histopathological criteria were used to diagnose the lung samples after tissue processing, the summarized features were based on observation of MPM images obtained from fresh, unprocessed tissue.
|Groups||Structural features at 760 nm||Spectral features at 760 nm|
|Normal lung (n=11)||Intact alveoli without a readily visualized cellular component||Intrinsic fluorescence from alveolar septa with emission peak ∼480 nm|
|Focal inflammation (n=3)||Cellular aggregations within alveolar lumens||Intrinsic cellular fluorescence at longer emission wavelengths (∼500 to 635 nm)|
|Adenomas (n=4)||Dense cellular masses that displace the lung parenchyma||Intrinsic cellular fluorescence predominantly at shorter emission wavelengths (∼420 to 460 nm)|
|Carcinomas (n=6)||Dense cellular masses that displace the lung parenchyma||Intrinsic cellular fluorescence predominantly at shorter emission wavelengths (∼420 to 460 nm); less pronounced fluorescence at 500 to 550 nm (lower Green/Blue ratio) compared to adenomas.|
Next, we evaluated the two-photon excited fluorescence patterns in MPM images from lung sites with diffuse and focal inflammation [Figs. 1(g)–1(l)]. Sites with diffuse inflammation showed readily identifiable individual cells infiltrating the alveolar lumina, whereas focal inflammations appeared as denser cellular accumulations without clearly visualized borders. Histopathology indicated that the cellular infiltration in the diffuse inflammation site was caused by macrophages, whereas the focal inflammatory lesion was composed of lymphocytes and macrophages. The cells in both the diffuse and focal inflammation site appeared yellow in MPM images, indicating fluorescence detected at longer wavelengths (500 to 635 nm, channel 2 and 3). Furthermore, two-photon excited emission spectra from groups of cells within the focal inflammation showed a pronounced red-shifted emission at both 760 and 860 nm excitation [Figs. 3(a) and 3(b)]. Denser cellular accumulations with intrinsic fluorescence emission at longer wavelengths were observed in MPM images from all focal inflammation sites and used as an MPM-detected feature to differentiate focal inflammatory sites and neoplastic cellular masses in this study (Table 1). Infiltration of cells fluorescing at longer emission wavelengths was also observed in the lung parenchyma next to most of the adenocarcinomas. Histopathological assessment indicated that the alveoli next to most adenocarcinoma were filled with macrophages with eosinophilic cytoplasm.
MPM of Diffuse Hyperplasia in Peripheral Mouse Lung
Precursor lesions, such as AAH, in the LSL-K-ras G12D lung adenocarcinoma model were previously described as an accumulation of atypical epithelial cells on alveolar walls.25 MPM images from peripheral lung with diffuse hyperplasia detected the accumulation of oval to cuboidal epithelial cells on alveolar walls (as confirmed by histopathology) without compression of the adjacent alveoli [Figs. 1(m)–1(o)]. At 760 nm excitation, these cells appeared blue in MPM images, indicating fluorescence detected predominantly at 420 to 460 nm. Furthermore, two-photon excited spectra from these cells displayed an emission peak at (data not shown), which is similar to emission maxima of spectra from the mouse tumors [Figs. 3(a) and 3(c)] and to values cited by previous publications on MPM of unprocessed tissue and attributed to cellular NADH.17,18
MPM of Mouse Lung Neoplasms Such as Adenomas and Adenocarcinomas
To elucidate the two-photon excited endogenous patterns of mouse lung neoplasms, we first imaged small adenomas (Fig. 4). In the H&E images, the adenomas appeared as well-demarcated nodules composed of neoplastic cuboidal epithelial cells that obliterated the alveolar spaces. MPM at 760 nm detected similar microanatomical patterns; the nodules appeared as dense cellular masses completely distorting the lung parenchyma, while the tissue immediately next to the nodule had intact alveoli. At 760 nm excitation, the majority of cells within the adenomas appeared blue in the MPM images, indicating fluorescence detected predominantly at 420 to 460 nm. Microspectroscopy confirmed that the two-photon excited fluorescence spectra from groups of cells within the adenomas peaked at [Figs. 3(a) and 3(c)]. Dense cellular aggregates with intrinsic fluorescence at 420 to 460 nm were observed in MPM images from all adenomas and described here as an MPM-detected feature (Table 1). At 860 nm excitation, the adenomas displayed an increased presence of fibers with dominant emission at 420 to 460 nm, as compared to the surrounding lung parenchyma [Figs. 4(c) and 4(f)]. This feature was visualized in three out of four adenomas. The adenoma that did not clearly display this feature was surrounded by lung parenchyma with diffuse hyperplasia.
MPM images from a mouse lung adenocarcinoma are shown in Fig. 5. At 760 nm excitation, most of the cells from a site within the tumor displayed dominant fluorescence emission at 420 to 460 nm, similar to the adenomas. More complex MPM patterns were observed at the periphery of the tumor [Fig. 5(h)] and the surrounding lung parenchyma [Fig. 5(k)] compared to the adenomas. In particular, the periphery of the lesion appeared to have cells with diverse structural and spectral patterns, while the surrounding lung parenchyma had marked infiltration of cells fluorescing at longer wavelengths. Histopathology confirmed the presence of focally extensive infiltrates of lymphocytes mixed with macrophages at the periphery of the lesion and marked macrophage infiltration in the surrounding alveoli. All adenocarcinomas in this study appeared as dense cellular masses in MPM images, and most of the cells within these masses displayed dominant cellular fluorescence emission at 420 to 460 nm. Therefore, the detection of cellular aggregates with dominant intrinsic fluorescence at 420 to 460 was described here as an MPM-detected characteristic of mouse adenocarcinomas (Table 1). At 860 nm excitation, the site within the adenocarcinoma [Fig. 5(f)] displayed more fibers with dominant emission at 420 to 460 nm, compared to the surrounding lung parenchyma [Fig. 5(l)]. Similar to the adenomas, this feature was detected by MPM at 860 nm in most (four out of six) adenocarcinomas and is likely to be SHG from collagen fibers at 430 nm. One of the adenocarcinomas that did not clearly display this feature was surrounded by lung parenchyma with diffuse hyperplasia. The biological basis for this feature has not been determined; however, advanced mouse lung adenocarcinomas are reported to deposit desmoplastic stroma around tumor cells28 and the observed fiber accumulation by MPM could signify increased stromal (fibrous) deposition.
Visual observation of MPM images at 760 nm showed that most of the cells within the adenomas and adenocarcinomas displayed dominant fluorescence emission at 420 to 460 nm. However, quantitative analysis of the MPM images revealed that, compared to cells within adenomas, cells within the adenocarcinomas displayed lower fluorescence emission at 500 to 550 nm, relative to fluorescence emission at 420 to 460 nm. In particular, we calculated the Green (500 to 550 nm)/Blue (420 to 460 nm) emission ratio (the average pixel intensity from the 500 to 550 nm channel vs. the average pixel intensity from the 420 to 460 nm channel) from MPM images of all adenomas and (the central regions) of all adenocarcinomas. On average, at 760 nm excitation, the cells within adenocarcinomas displayed a Green (500 to 550 nm)/Blue (420 to 460 nm) ratio that was lower than the adenomas (ratio for adenocarcinomas: , , ; ratio for adenomas: , , ). This indicates that, for the current set of MPM images, cells within the malignancies displayed a less pronounced fluorescence at 500 to 550 nm (blue-shifted fluorescence) compared to the benign tumors.
Spectroscopic Evaluation of Cells Within Mouse Lung Neoplasms and Focal Inflammatory Sites
To further elucidate differences in cellular fluorescence patterns of lung neoplasms and focal inflammations, we collected two-photon excited spectra from groups of cells from an adenoma, adenocarcinoma and focal inflammation [Fig. 3(a)]. At 760 nm excitation, cells from the adenocarcinoma showed similar emission at 400 to 460 nm, but less pronounced spectral broadening at 500 to 600 nm, compared to those from the adenoma. Cells from the focal inflammation showed a marked red-shifted fluorescence compared to cells from either the adenoma or adenocarcinoma, especially at longer emission wavelengths (500 to 640 nm). To determine the degree of variations between samples, average two-photon excited emission spectra were calculated from multiple samples for each histopathological category [Fig. 3(c)]. At 760 nm excitation, average spectra from the adenocarcinomas and adenomas showed similar cellular fluorescence at 400 to 460 nm, but different spectral emission at the 500 to 600 nm, confirming spectral trends observed from individual samples [Fig. 3(a)]. At 860 nm excitation, spectra from adenomas and adenocarcinomas displayed a similar emission peak and shape, whereas spectra from focal inflammations displayed a distinct red-shifted spectral broadening compared to all other categories. Spectroscopic trends summarized in Fig. 3 demonstrate that for the current data set, spectral differentiation between adenomas and adenocarcinomas was best achieved at 760 nm (and not at 860 nm) excitation and at 500 to 600 nm emission. However, focal inflammations were spectrally differentiated from lung neoplasms at both 760 and 860 nm excitation.
MPM of canine lung carcinoma
To confirm that our results were reproducible in spontaneously occurring lung carcinomas and applicable to larger mammals, we imaged normal and diseased lung tissue from a dog treated at Cornell University Hospital for Animals for bronchioloalveolar carcinoma of the left caudal lung lobe (Fig. 6). MPM images from an abnormal region with bronchioloalveolar carcinoma showed similar microanatomy to the H&E images, with cellular projections completely displacing the lung parenchyma. At 760 nm excitation, the cellular projections appeared blue in MPM images [Figs. 6(b) and 6(e)] and displayed emission spectra with a peak at [Fig. 6(m), blue lines]. MPM images from another region within the abnormal sample displayed accumulation of cells with yellow appearance (fluorescence at 500 to 635 nm). This region was histopathologically confirmed as cancer-associated inflammation. At 760 nm excitation, emission spectra from these cells displayed a red-shifted fluorescence compared to cells within the carcinoma region [Fig. 6(m), red lines]. By comparison, MPM of tumor-free peripheral lung detected intact alveoli without readily visualized cellular component. These features were similar to MPM detected characteristics of mouse normal, inflammatory and malignant lung and suggest that the MPM detected characteristics of mouse neoplasms (Table 1) would be also valid for spontaneously occurring lung carcinomas in larger mammals.
A preliminary step in evaluating MPM as a technique for early lung cancer detection requires studying the intrinsic two-photon excited fluorescence and SHG of lung and the selection of criteria from MPM images for lung nodules differentiation. We performed ex vivo MPM on unprocessed lung from mouse models of lung adenocarcinoma at differing stages of cancer development. Comparison of MPM and H&E images from the same region before and after tissue processing indicated that two-photon excited intrinsic fluorescence and SHG showed similar microanatomical information as standard histopathology. Detection of the two-photon excited fluorescence at three different emission regions also allowed visualizing the spectral characteristics of unprocessed normal and abnormal lung, not possible using standard histopathology. Our results have demonstrated that two-photon excited intrinsic fluorescence and SHG provide both structural and spectral contrast between normal, inflammatory, and neoplastic lung.
Structurally, mouse lung neoplasms are distinguished from tumor-free unaffected peripheral lung sites by an increased cellularity that is easily detected by MPM. Adenomas and adenocarcinomas appeared in MPM images as dense cellular masses that completely displaced the normal lung parenchyma. In contrast, the intrinsic fluorescence of tumor-free unaffected lung sites originated from intact alveoli without readily visualized cells (except for alveolar macrophages). These MPM-detected changes are in agreement with previous histological evaluation of mouse models of lung adenocarcinoma that characterize precursor lung lesions as an increased proliferation of cells along the alveolar septa that eventually form cellular masses, such as adenomas and adenocarcinomas.25 A previous MPM study on frozen human lung adenocarcinoma samples29 also detected increased cellularity in lung cancer nodules compared to unaffected peripheral lung. Our results demonstrate that MPM detects typical pathological changes in mouse lung microarchitecture caused by tumor progression without the need for tissue processing. Ex vivo label-free MPM of canine lung confirmed that similar microanatomical changes can also be observed in spontaneously occurring lung cancer in larger mammals.
Spectral data from MPM imaging demonstrated that mouse lung neoplasms have different intrinsic fluorescence compared to tumor-free unaffected lung. MPM at 760 nm excitation demonstrated that most cells within lung neoplasms displayed fluorescence detected predominantly at 420 to 460 nm. Two-photon excited emission spectra from cells within neoplasms peaked at , which is very similar to the emission peak wavelength of the cellular metabolic indicator, NADH.12,17–18 In comparison, two-photon excited spectra from tumor-free unaffected mouse lung sites had a different peak (, data not shown) and shape, suggesting a different origin of fluorescence. Therefore, MPM differentiated mouse adenomas and adenocarcinomas from tumor-free unaffected lung sites based on both structural (increased cellularity) and spectral (blue-shifted fluorescence) characteristics. This differentiation was observed in neoplastic and normal sites from two different mouse models and in resected canine lung tissue. This suggests that the described MPM characteristics are not particular to a specific lung cancer model and also would be valid for detecting spontaneously occurring lung carcinomas in larger mammals. We also showed that spectral MPM-detected characteristics differentiated benign from malignant neoplasms, an outcome not possible using only structural MPM-detected characteristics. Specifically, fluorescence emission ratio analysis of MPM images (and microspectroscopy) demonstrated that cells within adenomas displayed small spectral differences compared to cells within the malignancies. Together, these results demonstrate that MPM can be used as a microscopic technique to detect spectral, in addition to microanatomical, change in lung tissue with tumor progression.
MPM also demonstrated an increased cellularity with a distinct red-shifted fluorescence in mouse lung sites with diffuse or focal inflammation. As confirmed by histopathology, the cellular composition of these sites differed from that in tumors and consisted of inflammatory cells such as lymphocytes and/ or macrophages. MPM images from cancer related inflammatory sites from canine lung also showed cellular accumulations with red-shifted fluorescence compared to neoplastic cells. Porphyrin and lipofuscin, found in the vacuoles of macrophages, are fluorophores with dominant emission in the 505 to 655 nm range,30 and are likely responsible for the observed red-shifted fluorescence of inflammatory sites. The presence of cellular red-shifted emission in cellular aggregates in respiratory lung could serve as a marker to distinguish inflammatory nodules from lung neoplasms. For example, granulomas, benign nodules in humans composed of inflammatory cells, are likely to have red-shifted fluorescence when examined by MPM compared to lung adenocarcinomas.
Two-photon excited microspectroscopy from cells within lung neoplasms and inflammatory lung sites confirmed spectral trends observed in the MPM images. In particular, two-photon excited fluorescence spectra from inflammatory sites exhibited a large red spectral broadening compared to spectra from lung tumor sites in both mouse and canine samples. Microspectroscopy measurements from mouse neoplasms also showed, similar to the quantitative analysis of MPM images, that cells within benign tumors exhibit small spectral broadening compared to cells within malignant tumors. While these microspectroscopy results need to be further validated on samples from spontaneously occurring lung cancers, we provided initial evidence that two-photon excitation microspectroscopy, in addition to imaging, detects spectral differences between neoplastic and inflammatory lung sites. Therefore, two-photon excited fluorescence microspectroscopy could also be used as a clinically relevant technique to sample regions of interest within lung nodules for the minimally invasive differentiation of inflammatory from neoplastic lung sites.
We have demonstrated the feasibility of using MPM as a microscopic technique for detecting inflammation and cancer related changes in ex vivo mouse and canine lung. We expect that the described MPM-detected structural and spectral characteristics are also relevant for human lung, because the mouse models used in this study genetically and morphologically mimic human lung neoplasms. Results from the spontaneously occurring canine lung carcinoma further validated the relevance of the described MPM-detected characteristics for the minimally invasive imaging of lung neoplasms in larger mammals such as humans. Human lung tumors are usually diagnosed by sampling lung tissue with CT-guided needle biopsies and evaluating tissue samples by pulmonary cytology or histopathology. While this procedure yields accurate diagnosis for larger nodules, it has variable accuracy for small () and heterogeneous nodules. Additionally, it does not allow for direct, real-time assessment of the suspicious lesion. An endoscopic implementation of MPM to transthoracic (optical) needle biopsies or bronchoscopes would allow for the direct microscopic evaluation of nodules and possible real-time differentiation of benign from malignant lung sites. Fiber-coupled multiphoton endoscopes that detect intrinsic SHG from collagen and exogenous two-photon excited fluorescence from biological samples have already been reported.3132.–33 Several groups have also concentrated on designing fiber-coupled multiphoton endoscopes for the efficient detection of intrinsic fluorescence from unprocessed tissue. While we demonstrate MPM-detected differentiation between lung abnormalities, successful in vivo application will depend partially on the design of a MPM endoscope offering optimized collection of the weak endogenous fluorescence from optically attenuating tissues, such as the lung.
We thank Cheryl Balkman for recruiting the canine patient for this study and for help in obtaining the canine lung samples. We also thank the members of the Histology Laboratory at the College of Veterinary Medicine, Cornell University, for technical support and H&E slide preparation. This research was supported by US National Institutes of Health grants CA108773 (RSW) and R01-EB006736 (IP and WWW). SAY was supported through a DOD Breast Cancer Research Program predoctoral fellowship, and KRH was supported through a Cornell University College of Veterinary Medicine Clinical Fellow Award. Editorial help from Mark Williams is greatly appreciated.
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