This article reports on a detailed method for the dynamic measurement and quantification of blood flow velocity within individual blood vessels of the mouse liver vasculature using intravital microscopy imaging in combination with a specific methodology for image acquisition and analysis.
Intravital microscopy (IVM) is a powerful optical imaging technique that has made possible the visualization, monitoring and quantification of various biological events in real time and in live animals. This technology has greatly advanced our understanding of physiological processes and pathogen-mediated phenomena in specific organs.
In this study, IVM is applied to the mouse liver and protocols are designed to image in vivo the circulatory system of the liver and measure red blood cell (RBC) velocity in individual hepatic vessels. To visualize the different vessel subtypes that characterize the hepatic organ and perform blood flow speed measurements, C57Bl/6 mice are intravenously injected with a fluorescent plasma reagent that labels the liver-associated vasculature. IVM enables in vivo, real time, measurement of RBC velocity in a specific vessel of interest. Establishing this methodology will make it possible to investigate liver hemodynamics under physiological and pathological conditions. Ultimately, this imaging-based methodology will be important for studying the influence of L. donovani infection on hepatic hemodynamics.
This method can be applied to other infectious models and mouse organs and might be further extended to pre-clinical testing of a drug’s effect on inflammation by quantifying its effect on blood flow.
Organ-specific hemodynamics are important physiological features of any mammalian organ. Abnormalities in blood flow may be the consequence of inflammation and a sign of organ dysfunction1. Thus, blood flow organization, structure and function appear as critical parameters for analysis under physiological and pathological conditions. The techniques that have been commonly used for analyzing blood flow in a specific organ contain several limitations, including the resolution limit of the technique itself (e.g. Doppler imaging of blood flow), the capacity for measurement of absolute blood flow only (volume of blood per unit serving an organ) (e.g. Optical Coherence tomography) and the measurement of average changes in speed in a large and heterogeneous population of blood vessels2,3. The liver’s circulatory system links different vessel subtypes that are heterogeneous in their size, structure and function. In this study, intravital microscopy (IVM) imaging technology is applied to evaluate liver hemodynamics in vivo, in real time, at high resolution and in parallel to uncover the characteristics of the individual blood vessels that comprise the hepatic organ. The recent development of this powerful optical imaging technique allows the researcher to collect dynamic data on living animals at a high spatial and temporal resolution. By allowing the direct visualization and real time monitoring of specific and rapid biological processes in vivo, IVM provides a unique opportunity to the researcher to image individual blood vessels, and measure and quantify the velocity of single red blood cells (RBC) within a specifically selected hepatic vessel.
In this study, we have implemented the IVM technique in the mouse liver to investigate the influence of mouse infection by the hepatotropic Leishmania parasite on liver hemodynamics. L. donovani is the agent responsible for visceral leishmaniasis, a severe disease characterized by acute-on-chronic inflammatory responses and a pathology that is present in multiple organs, including the spleen and the liver. In an experimental mouse model of visceral leishmaniasis, the liver infection is self-resolving whereas the splenic infection is progressive4. These outcomes of Leishmania infection with respect to the individual organs are still not completely understood. Investigation of liver and spleen hemodynamics under pathological conditions will shed new light on host-parasite interactions and disease pathogenesis.
Our experimental model system is based on exposing and imaging the liver of an anesthetized mouse that received intravenous injection of specific fluorescent dyes for the labeling of the hepatic intravasculature. The liver is a favorable organ for intra-vital microscopy. After performing a small incision in the abdomen, the liver is gently externalized and placed on wet gauze, then on a coverslip with the goal of reducing any motion artifacts due to heartbeat and respiration. The liver is then placed within the view of a microscope lens. As compared to the spleen and lymph node which require the use of two photon microscopy for IVM studies, the advantage of the liver lies in its homogenous 3D architecture/anatomy that allows for the use of a conventional confocal microscope, with a maximum penetration depth of approximately 50 μm, for intravital microscopy imaging5-8.
This study describes two independent imaging methods for the quantitative measurement of RBC velocity and blood flow speed in individual blood vessels. In the first method, liver blood flow is acquired using a xy bi-dimensional mode over time. The resulting xyt data are analyzed using the MtrackJ plugin in the free ImageJ software, which allows for the tracking of individual RBCs over time. In the second method, a single blood vessel is selected and its corresponding blood flow is analyzed using the line scanning fast acquisition mode of the confocal laser-scanning microscope. The vessel of interest is scanned at high frequency along its central axis through an axial line. The blood flow velocity is then quantified based on the difference in contrast between unlabeled dark erythrocytes and fluorescently labeled plasma. The fluorescence intensities of RBCs and plasma acquired along the line scan are plotted against time to obtain streaks, the angles of which are proportional to the velocities of an individual RBC.
The goal of this article is to provide a simple and reproducible method for imaging and measuring blood flow velocity within individual blood vessels of the liver and to make available the basic tools for the successful performance of mouse surgery, IVM and quantitative analyses of the velocity of individual RBCs. This approach will allow researchers to gain new insights into blood velocity under pathological conditions.
Ethics statement: All the animal studies were performed in accordance with guidelines and protocols that were approved by the Institutional Animal Care and Use Committee of the Aix-Marseille Université, France. Female C57Bl/6 mice at 8 – 10 weeks old were commercially obtained and handled according to the rules of Décret N° 8 87–848, October 19, 1987, Paris. All the experiments using L. donovani LD1S parasites were conducted in accordance with biosafety regulations from the French and European Union legislation.
1. Mouse Infection with L. donovani Promastigote Parasites
2. Surgical Procedures
3. Intravital Microscopy Imaging of the Liver Architecture
4. Intravital Microscopy Imaging of the Liver for Blood Flow Speed Measurement
5. Quantitative Analysis of RBC Velocity Using the xyt Images (Method 1)
6. Quantitative Analysis of RBC Velocity Using the xt Line Images (Method 2)
The specific architectural organization of the sinusoids in the liver can be visualized based on the autofluorescent property of this organ (Figure 1, panel B and C, green), the intraperitoneal injection of Hoechst for the labeling of hepatocyte nuclei (Figure 1B, blue) and the intravenous injection of fluorescent BSA for the staining of the hepatic circulatory system (Figure 1C, red). The liver is composed of several different vessel subtypes with different functions and structures and sizes ranging from 40-700 μm2 in diameter (D) (D of small vessels is between 40-80 μm2 and D of large vessels is above 300 μm2). Intravital microscopy imaging of the liver allows for the visualization at high resolution of the heterogeneity and complexity of the liver vasculature (Figure 1C).
To monitor blood flow speed in individual vessels, two different methodologies are used for the image acquisition and data analysis of the liver blood vessels in vivo. In the first method, real-time imaging of the blood flow in a vessel of interest is performed using the xyt scanning mode (Movie 1). Quantitative analysis of the velocity of an individual RBC in a single vessel is performed using the MTrackJ plugin in the ImageJ software (Figure 2A and 2B). A minimum of five particles per vessel is tracked in different vessels ranging from 40-80 μm2 of diameter. The results obtained with this method give consistent and reproducible values across different mice and evaluate the RBC velocity in small liver vessels at values between 25-35 μm/sec (Figure 2C).
The second method consists of repeatedly scanning along a line parallel to the vessel wall, with the line placed in the center of the vessel lumen. Figure 3 shows a xy frame scan (left panels) with the corresponding xt line scan (right panels). The velocity of an individual RBC is given by the ratio V = distance/time and is calculated using the orthogonal projections on the X and Y axis of the streak obtained in the xt image. In Figures 3D and 3E, each data point represents the velocity of an individual RBC from different small or large vessels selected from different mice. As seen from the error bars, the data show a relatively low variation between RBC velocities and indicate that blood flow speed is dramatically faster in large vessels than in small vessels. In addition, a significant variation in the velocity values obtained from different types of large vessels was observed whereas blood flow speed is relatively similar across different types of small vessels. Blood flow measurements with this newer method generate data that is comparable to data obtained from the previously described method using MTrackJ (compare Figure 2C 세스 Figure 3D). The image in Figure 3C represents a typical example of a suboptimal experiment in which the xy frame scan generates an un-interpretable xt image. In this particular case, the problem results from both i) the fast internalization of BSA into the endothelial cells lining the vessel of interest and ii) the presence of a junction between two vessels that perturbs the blood flow in the selected area of acquisition. The rate of internalization of the plasma reagent into the endothelium lining the blood vessel is a critical parameter to consider when measuring blood flow speed, as internalization will alter the quality of the xt image that shows the streaks. The internalization rate critically depends on the dose of the dye that is intravenously injected. In Figure 4 we show that 500 μg of BSA-Alexa 647 and/or 500 kDa of Dextran-FITC are the optimal doses that should be used for the quantification of blood flow speed. These doses generate a very bright signal that allows for the identification of the RBC as dark particles against a bright background and enable the visualization of blood flow for a minimum of 1 hr without internalization of the injected dye (Figure 4, bottom panel). In contrast, 50 μg of BSA-Alexa 647 and/or 500 kDa Dextran-FITC (not shown), while allowing for the visualization of the liver’s vascular network, is a suboptimal dose for measuring blood flow velocity due to the very fast internalization of the dye, which starts at 5 min post-injection (Figure 4, bottom panel).
When applying this methodology to the liver of infected animals, we observed a significant increase in the blood flow velocity as soon as 1 hr post-infection. Alteration of the RBC velocity is maintained up to 24 hr post-infection. It ultimately reaches normal values at 72 hr post-parasite injection (Figure 5). Thus, this experiment validates the use of this methodology to gain new insights into the influence of pathological conditions on liver hemodynamics.
Figure 1: Intravital Microscopy of the Mouse Liver. (A) Liver surgery of the mouse. A small area of a liver lobe is exposed after surgery, two moist gauze pieces are placed around it and a slide is put on the abdomen to cover the liver prior to the mouse being placed on the stage of a confocal microscope. (B, C) Image of a representative area of the liver of a non-infected mouse that demonstrates the liver sinusoids and the different sizes of the vessels that comprise the hepatic organ. Liver autofluorescence is shown in green. The mouse is injected with Hoechst 33342 (blue) to label the hepatocyte nuclei (B) and injected with BSA-Alexa 647 (red) to visualize the liver vasculature (C). Scale bars, 50 μm Please click here to view a larger version of this figure.
Figure 2: Quantitative Analysis of RBC Velocity from a xy Frame Scan using the ImageJ Software. (A) Representative xy image of blood circulation in a small liver vessel acquired by intravital microscopy imaging of the mouse liver using the fast xy scanning mode. Dark areas correspond to RBCs. Scale bar, 10 μm. (B) Quantification of the velocity of a single RBC using the MTrackJ plugin from ImageJ. Lines (red, yellow, white) represent the trajectory over time of an individual RBC. (C) RBC velocity in individual small (D is approximately 50 μm2) hepatic vessels. The graph plots the value of the velocity of five independent RBCs tracked in individual liver vessels that were selected from five different mice (1 to 5). D represents the diameter of the vessel in μm2. Please click here to view a larger version of this figure.
Figure 3: Liver Blood Flow Measurements by Intravital Microscopy Imaging of a Blood Vessel using the xt Line Scanning Mode. Representative xy images (left panels) of liver vessels labeled with BSA-Alexa 647 and their corresponding xt images (right panels) obtained from a line-scan of the central lumen of an individual vessel. (A, B) Small (A) and large liver vessel (B). (C) Representative data from a sub-optimal experiment showing the intersection of two blood vessels and BSA internalization into the endothelium. (D, E) The graphs plot the value of the velocity of three independent RBCs per vessel (small in D and large in E) selected from five different mice. D represents the diameter of the vessel in μm2. Please click here to view a larger version of this figure.
Figure 4: The Effect of the Dose of the Fluorescent Plasma Dye on Its Internalization into the Endothelium Lining the Sinusoids. This image tracks the internalization of BSA and Dextran 500 kDa into the endothelium lining the sinusoids, as a function of time and injection dose. Please click here to view a larger version of this figure.
Figure 5: Effect of L. donovani infection on Liver Hemodynamics. This graph plots the values of the blood velocity obtained from several individual blood vessels from non-infected mice (NI) and mice that were infected with L. donovani and analyzed 1 hr, 24 hr and 72 hr post-infection (pi). Each dot represents the mean value of five RBC velocity measurements obtained in a single blood vessel of approximately 50 μm2. In each condition (NI, 1 hr pi, 24 hr pi and 72 hr pi) a minimum of three mice were analyzed for blood flow speed. The stars indicate a significant difference in the blood flow speed obtained 1 hr and 24 hr pi compared to NI mice (P <0.01, one way Anova).
Movie 1.Time-lapse Intravital Microscopy Imaging of the Mouse Liver. Movie 1 corresponds to Figure 3. The mouse received an injection of BSA-Alexa 647 to visualize the vasculature. Blood flow in three small vessels (D of 50 μm2) is shown. Black areas correspond to RBC.
The recent development of intravital microscopy of the mouse liver opens up new possibilities for the investigation of physiological response to infection in vivo and in real time5,9,10. Organ blood flow is a critical physiological parameter that is often altered in many diseases. However, the status of liver hemodynamics under physiological and infectious conditions remains a poorly explored area. In this study, IVM-based methods, which were previously adapted for the study of the spleen and tumor vasculature, were implemented to quantify liver blood flow speed within a single vessel and measure individual RBC velocity in vivo11,12. The methodologies used here rely on the contrast between a plasma fluorophore injected intravenously in the mouse, such as fluorescent BSA, and the erythrocytes, which remain dark. In vivo blood flow measurements have the potential to improve our understanding of disease processes.
Here, two methodologies were used and compared to measure blood flow in liver vessels. The first methodology is time consuming and fastidious in term of data analysis as it requires users to manually track RBC movement in an individual vessel using the MTrackJ plugin in the ImageJ software. The second methodology is simple and fast, as it consists of the analysis of an xt image of a blood vessel generated from a line scan acquisition with resonant scanner mode. The two methodologies give comparable data for similar vessels. At this stage it is almost impossible to compare our data with others, as, to our knowledge, blood flow speed has never been quantified in such small vessels and in mouse sinusoid capillaries with a width of approximately 10 μm. IVM-based methods allow high resolution in xy of 500 nm enabling the analysis of a sinusoid with a width of 10-50 μm 13. In contrast, Doppler-based techniques only have a maximal resolution of 70 μm, thus limiting the measurement of the blood flow to liver arteries and portal veins 3.
One of the main steps that is critical for the successful implementation of these methodologies is a successful surgery and maintenance of the anesthetized mouse in good physiological condition during the entire imaging session. To do so, one must carefully control the temperature of the microscope chamber and inject anesthetic every hour. Another critical step is the internalization of the fluorescent plasma reagent into the endothelium lining that can occur naturally after its injection. Such internalization will produce uninterpretable xt images and un-contrasted xy images. This phenomenon depends on the dose of the injected dye and can be prevented by injecting a high dose of the plasma reagent (Figure 4).
Importantly, successful intravital microscopy imaging of the liver blood flow requires the consideration of several critical aspects. These include the complexity of the liver vasculature system, the presence of different subtypes of blood vessels containing small and large vessels with different structures and functions, different blood circulations with fast and slow flux and rapid RBC velocities. The main limitation of the methodology that is based on the analysis of a xt image is the speed of acquisition of the vessel and the lack of Z resolution, as the image is acquired in 3D (xyt). More specifically, the line scan rates of standard systems reach a limit of sensitivity with regard to the acquisition of large blood vessels (diameter above 180 μm2) that are characterized by very high RBC velocities, which is the case with arteries. In the large vessel, the RBC trajectory can be out of the imaged plane and any components that are perpendicular to the scanned plane will be excluded from the analysis.
The methodology presented here represents an ideal tool for the in vivo and real time quantification of several blood flow parameters under various pathological conditions. The investigation of liver hemodynamics will shed new light on disease processes and parasite pathogenesis in a specific organ. Our efforts to gain insights into the liver microvasculature system applied to an experimental mouse model of Leishmania infection opens up the possibility for the correlation of several blood flow parameters with parasite multiplication and disease development in this organ, in real time. The further development of reagents, tools and the methodology for the improved characterization of the liver’s vasculature system by IVM during infection is of great importance for the study of the influence of parasite colonization on this physiological parameter and, reciprocally, the influence of blood flow on Leishmania pathogenesis. This strategy can be potentially extended to other infectious systems where pathogens target the liver.
The authors have nothing to disclose.
This research was supported by the INSERM, the University of Aix-Marseille and a Career Development award from HFSPO obtained by CL Forestier.
Hoechst 33342 | Sigma Aldrich | B2261 | |
BSA-Alexa 647 | lifetechnologies | A34785 | |
Dextran-FITC 500 mol wt | SIGMA | 46947 | |
Ketamine | PanPharma | 20434 | |
Xylazine | Bayer | KP07KEU | |
Vetedine | Pharma Animal | 6869029 | |
Cyanoacrylate liquid | Cyanolit | 5833300005 | |
Coverslip frame: Membrane slide for microdissection part N°: 5013 | Molecular machines | 50103 | |
Coverslip DiaPath 24×60 ep: 1.6 mm | DiaPath | 61061 | |
Confocal laser scanning microscope | Leica | TCS-SP5 | |
LAS-AF viewer | Leica software | Version 3.1.0 buid 8587 |