Antibody-labeled fluorescence imaging of dendritic cell populations in vivo

We report an optical molecular imaging technique that exploits local administration of fluorophore-conjugated antibodies and confocal fluorescence microscopy to achieve high-contrast imaging of host cell populations in normal and tumor tissue in living mice. The method achieves micron-scale spatial resolution to depths greater than 100 μm. We illustrate the capabilities of this approach by imaging two dendritic cell populations in the skin and normal and tumor vasculature in vivo. Noninvasive imaging offers critically important windows into cell and tissue structure and function, normal and diseased physiology, and responses to therapeutic intervention. An explosion of imaging methods has occurred in recent decades, and applications span a wide range of biomedical specialties. Optical imaging, while limited with respect to the depths it can probe, offers exquisite spatial resolution and molecular specificity. In vivo applications of optical coherence and fluorescence tomography, reflectance and fluorescence confocal imaging, and multiphoton imaging are all undergoing rapid expansion.^{1, 2} Biologically important optical signals arise from endogenous chromophores and light-matter interactions³ and from exogenously administered labels targeting molecular or cellular structure or function.^{4, 5} Trafficking of immune cells in normal and malignant tissue is an area of intense interest, in which conventional technologies such as immunohistochemistry have provided extensive information. New in vivo techniques based on intravital confocal and multiphoton microscopy have revealed amazing images of immune cell interactions, such as those between antigen-presenting dendritic cells (DCs) and T cells, in surgically exposed lymph nodes.^{6, 7, 8, 9} Exploiting the unique morphology of dendritic cells, a recent study reported the use of reflectance confocal microscopy to image the distribution of epithelial DCs in human cornea in vivo.¹⁰ Langerhans cells (LCs) and other DCs in the skin are important, as they are often the first to encounter antigen. These cells are of particular consideration from an imaging standpoint in that they are directly accessible via optical methods. Recently, we demonstrated a fresh whole-mount immunolabeling method that enables multicolor imaging of tumor and normal tissue vasculature and lymphatics, host cell populations, and extracellular matrix with minimal perturbation of tissue architecture.¹¹ Here, we describe the extension of a fluorophore-conjugated-antibody-labeling-based confocal fluorescence imaging method to living mice and use the technique to identify LC and dermal or interstitial DC (iDC) trafficking in normal ear and in an intradermal murine tumor model. Within $2\mathrm{h}$ after direct intradermal injection of antibody, the method yields images with very high contrast and confocal image resolution to depths of at least $100\mu \mathrm{m}$ in living tissue. Excellent staining persists for a minimum of $3\text{to}6\mathrm{h}$ following a single injection. Although these two DC populations are labeled using the same antibody directed against the major histocompatibility complex class II (MHC-II), they are distinguished unambiguously on the basis of their distinct morphologies and their stratification in the epidermal and dermal layers of the skin.¹² Prior to injection of fluorophore-conjugated antibodies, hair on the ears of BALB/c mice was removed by a chemical depilatory agent. One day after hair removal, the mice were anesthetized, and the ears were injected intradermally on the ventral side with $40\mu \mathrm{l}$ of an antibody cocktail consisting of phosphate buffered saline (PBS), Fc block ( $0.35\mathrm{mg}∕\mathrm{ml}$ ; BD Biosciences, San Diego, California), allophycocyanin (APC)-conjugated $\mathrm{anti}\left(\alpha \right)\mathrm{MHC}\text{-}\mathrm{II}$ ( $0.05\mathrm{mg}∕\mathrm{ml}$ ; eBioscience, Inc., San Diego), and AlexaFluor488-conjugated $\alpha \mathrm{CD}31$ ( $0.05\mathrm{mg}∕\mathrm{ml}$ ; Biolegend, San Diego). The first of these antibodies labels the two morphologically distinct yet related antigen-presenting cells—the LCs within the epidermis and iDCs in the dermis.¹⁰ The second labels the adhesion molecule PECAM, which is highly expressed on blood vessels and less intensely expressed on lymphatic vessels. Vessels reside only in the dermal layer, and labeling them contributes to the identification of the two DC populations. After $2\mathrm{h}$ to allow for the unlabeled antibody to clear, the mice were again anesthetized for imaging. In vivo imaging was performed using a custom inverted laser scanning confocal fluorescence microscope.^{13, 14} We have recently reported on the use of the antibody labeling technique in conjunction with the confocal imaging system to visualize the intratumor distribution of a photodynamic therapy sensitizer in vivo with respect to fluorophore-labeled CD31-positive vessels.¹⁵ In this study, to image the two DC populations and CD31-positive vessels, we used sequential two-color excitation of identical fields of view; APC was excited with a $639\text{-}\mathrm{nm}$ diode laser, and Alexa488 was excited with $488\mathrm{nm}$ from an argon-ion laser. The APC and Alexa488 emissions were detected using a 647LP long-pass filter and a $515∕30$ bandpass filter, respectively. The combination of a $100\text{-}\mu \mathrm{m}$ -diam pinhole and a $10\times$ , $0.45\mathrm{NA}$ objective gave an optical section thickness of approximately $6\mu \mathrm{m}$ , as determined by fluorescence edge response measurements.¹³ The images were acquired with a lateral resolution of $1\mu \mathrm{m}\text{per}\text{pixel}$ . The mice were placed on the stage in the supine position so that the ventral side of the ear was facing downward for imaging. Confocal images were then acquired every $3\mu \mathrm{m}$ , beginning at an initial depth of roughly $30\mu \mathrm{m}$ from the surface. The images could then be analyzed individually or as a three-dimensional (3-D) volume. For all experiments, the appropriate isotype controls were used to rule out nonspecific staining. Confocal fluorescence images obtained in vivo show positive staining for both DC types, as evident by their unique morphologies at depths consistent with their localization in epidermal or dermal layers. Within the epidermis at a depth of approximately $40\mu \mathrm{m}$ from the surface of the ear, an extensive mesh-network of densely packed LCs with characteristic long dendritic-like projections¹² is shown in Fig. 1a . Optical sections acquired in the dermis at depths of approximately $80\mu \mathrm{m}$ [Fig. 1b] show that the LC population is no longer present and that it is replaced by a stout, relatively sparse iDC population lacking long projections. Also evident in Fig. 1b and exclusive to the dermis is the extensive vasculature system, which is labeled with $\alpha \mathrm{CD}31$ antibody and which serves as a useful biomarker to discriminate dermal from epidermal layers. We note that the iDCs tend to cluster tightly in the vicinity of the vasculature. <!-- named anchor --> Fig. 1 In vivo confocal fluorescence images of $\mathrm{MHC}\text{-}{\mathrm{II}}^{+}$ cells in the mouse ear reveal two morphologically distinct cutaneous DC populations in superficial epidermal (a) and deeper dermal (b) layers of the tissue. In (b), dermal vessels are labeled with Alexa488-conjugated $\alpha \mathrm{CD}31$ . (c) to (f) Ex vivo whole-mount histology confirms in vivo observations. Excised ears were split and processed; the epidermis was stained with $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ (c) and $\alpha \text{langerin}$ (d) to confirm the identification and morphology of Langerhans cells. Image overlay (e) confirms the dual staining. (f) DCs in the dermis were stained with $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ (red), and their distribution relative to $\alpha \mathrm{CD}31$ -labeled vessels (green) is shown. These findings were confirmed in 10 and 20 mice for in vivo confocal and whole-mount imaging, respectively. The field of view in all images is $380\mu \mathrm{m}\times 380\mu \mathrm{m}$ . To confirm the identification of the DC populations imaged in vivo, we used whole-mount labeling of ex vivo tissues obtained from the dermal and epidermal layers of the ear and conventional fluorescence microscopy. Although both LCs and iDCs are MHC-II positive on their cell surfaces, only the LCs are positive for internal langerin, a C-type lectin unique to the cell and crucial for its development.¹⁶ Briefly, mice were sacrificed, ear hair was chemically removed, and ears were excised and split with the aid of forceps into dorsal and ventral halves. For dermal labeling, split ears were placed in $200\mu \mathrm{l}$ of PBS with Fc Block $(28.6\mu \mathrm{g}∕\mathrm{ml})$ , APC-conjugated $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ $(7.5\mu \mathrm{g}∕\mathrm{ml})$ , and phycoerythrin (PE)-conjugated $\alpha \mathrm{CD}31$ $(7.5\mu \mathrm{g}∕\mathrm{ml})$ and stained for $2\mathrm{h}$ at $4°\mathrm{C}$ . To label the epidermis exclusively, additional tissue processing was required. Following ear splitting, halves were floated in $0.5\mathrm{M}$ ammonium thiocyanate at $37°\mathrm{C}$ for $20\min$ to separate epidermal from dermal layers. The epidermal layer was then fixed in 2% paraformaldehyde at room temperature for $15\min$ to permeabilize the cells to enable labeling of internal langerin. Epidermal tissue was then incubated for $2\mathrm{h}$ with PE-conjugated $\alpha \text{langerin}$ $(7.5\mu \mathrm{g}∕\mathrm{ml})$ and APC-conjugated $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ $(7.5\mu \mathrm{g}∕\mathrm{ml})$ . Positive staining of epidermal whole mounts with both $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ [Fig. 1c] and internal $\alpha \text{langerin}$ [Fig. 1d] confirms the identification of these epidermal LCs. This critical confirmation can be performed only ex vivo, as cell permeabilization is not possible in vivo. The significant overlap between the images of the cell surface and internal markers for LCs is depicted in Fig. 1e. Single-color control experiments revealed no detectable cross talk between these two detection channels. The long cellular processes characteristic of these LCs are apparent in both the images obtained from the epidermal whole-mount preparation and from the superficial optical sections in vivo [Fig. 1a]. Ex vivo fluorescence imaging of the dermal layer [Fig. 1f] reveals vascular and DC cell morphology features similar to those observed in the images obtained from the deeper, dermal skin layer in vivo [Fig. 1b]. We have also implemented this technique to examine the tumor microenvironment in EMT6 mammary tumors grown intradermally in the ears of BALB/c mice. Tumors were initiated with an intradermal injection of $2\times {10}^5$ EMT6 cells and grown to a diameter of approximately $3\mathrm{mm}$ . $\mathrm{MHC}\text{-}{\mathrm{II}}^{+}$ cells and tumor blood vessels were labeled with APC-conjugated $\alpha \mathrm{MHC}\text{-}\mathrm{II}$ and Alexa488-conjugated $\alpha \mathrm{CD}31$ , respectively, using intradermal injection of the antibody cocktail described earlier. As illustrated in Fig. 2 , in vivo confocal images acquired at two different depths $2\mathrm{h}$ after antibody administration revealed excellent, high-contrast staining of $\mathrm{MHC}\text{-}{\mathrm{II}}^{+}$ cells. Specifically, the signal levels from stained cells observed in Figs. 2a and 2c are at least...