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1.
J Neuroinflammation ; 20(1): 206, 2023 Sep 09.
Article in English | MEDLINE | ID: mdl-37689689

ABSTRACT

BACKGROUND: Retinal degeneration is a disease affecting the eye, which is an immune-privileged site because of its anatomical and physiological properties. Alterations in retinal homeostasis-because of injury, disease, or aging-initiate inflammatory cascades, where peripheral leukocytes (PL) infiltrate the parenchyma, leading to retinal degeneration. So far, research on PL's role in retinal degeneration was limited to observing a few cell types at specific times or sectioning the tissue. This restricted our understanding of immune cell interactions and response duration. METHODS: In vivo microscopy in preclinical mouse models can overcome these limitations enabling the spatio-temporal characterization of PL dynamics. Through in vivo imaging, we assessed structural and fluorescence changes in response to a focal injury at a defined location over time. We also utilized minimally invasive techniques, pharmacological interventions, and knockout (KO) mice to determine the role of PL in local inflammation. Furthermore, we investigated PL abundance and localization during retinal degeneration in human eyes by histological analysis to assess to which extent our preclinical study translates to human retinal degeneration. RESULTS: We demonstrate that PL, especially T cells, play a detrimental role during retinal injury response. In mice, we observed the recruitment of helper and cytotoxic T cells in the parenchyma post-injury, and T cells also resided in the macula and peripheral retina in pathological conditions in humans. Additionally, we found that the pharmacological PL reduction and genetic depletion of T-cells reduced injured areas in murine retinas and rescued the blood-retina barrier (BRB) integrity. Both conditions promoted morphological changes of Cx3cr1+ cells, including microglial cells, toward an amoeboid phenotype during injury response. Interestingly, selective depletion of CD8+ T cells accelerated recovery of the BRB compared to broader depletions. After anti-CD8 treatment, the retinal function improved, concomitant to a beneficial immune response. CONCLUSIONS: Our data provide novel insights into the adaptive immune response to retinal injury in mice and human retinal degeneration. Such information is fundamental to understanding retinal disorders and developing therapeutics to modulate immune responses to retinal degeneration safely.


Subject(s)
Retinal Degeneration , Humans , Animals , Mice , CD8-Positive T-Lymphocytes , Retina , Leukocytes , Aging
2.
PLoS One ; 16(8): e0255204, 2021.
Article in English | MEDLINE | ID: mdl-34351959

ABSTRACT

Advances in intravital microscopy (IVM) have enabled the studies of cellular organization and dynamics in the native microenvironment of intact organisms with minimal perturbation. The abilities to track specific cell populations and monitor their interactions have opened up new horizons for visualizing cell biology in vivo, yet the success of standard fluorescence cell labeling approaches for IVM comes with a "dark side" in that unlabeled cells are invisible, leaving labeled cells or structures to appear isolated in space, devoid of their surroundings and lacking proper biological context. Here we describe a novel method for "filling in the void" by harnessing the ubiquity of extracellular (interstitial) fluid and its ease of fluorescence labelling by commonly used vascular and lymphatic tracers. We show that during routine labeling of the vasculature and lymphatics for IVM, commonly used fluorescent tracers readily perfuse the interstitial spaces of the bone marrow (BM) and the lymph node (LN), outlining the unlabeled cells and forming negative contrast images that complement standard (positive) cell labeling approaches. The method is simple yet powerful, offering a comprehensive view of the cellular landscape such as cell density and spatial distribution, as well as dynamic processes such as cell motility and transmigration across the vascular endothelium. The extracellular localization of the dye and the interstitial flow provide favorable conditions for prolonged Intravital time lapse imaging with minimal toxicity and photobleaching.


Subject(s)
Contrast Media/chemistry , Intravital Microscopy , Animals , Automation , Bone Marrow/diagnostic imaging , Female , Fluorescent Dyes/chemistry , Lymph Nodes/diagnostic imaging , Male , Mice, Inbred C57BL , Microscopy, Fluorescence , Regional Blood Flow , Time Factors
3.
J Biomed Opt ; 24(8): 1-11, 2019 08.
Article in English | MEDLINE | ID: mdl-31456386

ABSTRACT

Circulating tumor cells (CTCs) are of great interest in cancer research because of their crucial role in hematogenous metastasis. We recently developed "diffuse in vivo flow cytometry" (DiFC), a preclinical research tool for enumerating extremely rare fluorescently labeled CTCs directly in vivo. In this work, we developed a green fluorescent protein (GFP)-compatible version of DiFC and used it to noninvasively monitor tumor cell numbers in circulation in a multiple myeloma (MM) disseminated xenograft mouse model. We show that DiFC allowed enumeration of CTCs in individual mice overtime during MM growth, with sensitivity below 1 CTC mL − 1 of peripheral blood. DiFC also revealed the presence of CTC clusters (CTCCs) in circulation to our knowledge for the first time in this model and allowed us to calculate CTCC size, frequency, and kinetics of shedding. We anticipate that the unique capabilities of DiFC will have many uses in preclinical study of metastasis, in particular, with a large number of GFP-expressing xenograft and transgenic mouse models.


Subject(s)
Microscopy, Confocal , Multiple Myeloma/blood , Multiple Myeloma/diagnostic imaging , Neoplastic Cells, Circulating , Animals , Fluorescence , Green Fluorescent Proteins/metabolism , Humans , Kinetics , Male , Mice , Mice, SCID , Mice, Transgenic , Neoplasm Metastasis , Neoplasm Transplantation , Phantoms, Imaging
4.
Sci Rep ; 9(1): 3366, 2019 03 04.
Article in English | MEDLINE | ID: mdl-30833671

ABSTRACT

Circulating tumor cells (CTCs) are of great interest in cancer research, but methods for their enumeration remain far from optimal. We developed a new small animal research tool called "Diffuse in vivo Flow Cytometry" (DiFC) for detecting extremely rare fluorescently-labeled circulating cells directly in the bloodstream. The technique exploits near-infrared diffuse photons to detect and count cells flowing in large superficial arteries and veins without drawing blood samples. DiFC uses custom-designed, dual fiber optic probes that are placed in contact with the skin surface approximately above a major vascular bundle. In combination with a novel signal processing algorithm, DiFC allows counting of individual cells moving in arterial or venous directions, as well as measurement of their speed and depth. We show that DiFC allows sampling of the entire circulating blood volume of a mouse in under 10 minutes, while maintaining a false alarm rate of 0.014 per minute. In practice, this means that DiFC allows reliable detection of circulating cells below 1 cell per mL. Hence, the unique capabilities of DiFC are highly suited to biological applications involving very rare cell types such as the study of hematogenous cancer metastasis.


Subject(s)
Flow Cytometry/methods , Neoplastic Cells, Circulating/pathology , Algorithms , Animals , Arteries , Blood Flow Velocity , Cell Count/methods , Fluorescent Dyes , Mice , Neoplasm Metastasis/diagnostic imaging , Optical Fibers , Veins
5.
Sci Rep ; 7(1): 3875, 2017 06 20.
Article in English | MEDLINE | ID: mdl-28634334

ABSTRACT

Transplantation of a single hematopoietic stem cell is an important method for its functional characterization, but the standard transplantation protocol relies on cell homing to the bone marrow after intravenous injection. Here, we present a method to transplant single cells directly into the bone marrow of live mice. We developed an optical platform that integrates a multiphoton microscope with a laser ablation unit for microsurgery and an optical tweezer for cell micromanipulation. These tools allow image-guided single cell transplantation with high spatial control. The platform was used to deliver single hematopoietic stem cells. The engraftment of transplants was tracked over time, illustrating that the technique can be useful for studying both normal and malignant stem cells in vivo.


Subject(s)
Bone Marrow Cells/cytology , Bone Marrow Cells/metabolism , Bone Marrow Transplantation , Molecular Imaging , Single-Cell Analysis , Animals , Mice , Mice, Transgenic , Single-Cell Analysis/methods
6.
Science ; 354(6316): 1156-1160, 2016 12 02.
Article in English | MEDLINE | ID: mdl-27738012

ABSTRACT

A single hematopoietic stem cell (HSC) is capable of reconstituting hematopoiesis and maintaining homeostasis by balancing self-renewal and cell differentiation. The mechanisms of HSC division balance, however, are not yet defined. Here we demonstrate, by characterizing at the single-cell level a purified and minimally heterogeneous murine Tie2+ HSC population, that these top hierarchical HSCs preferentially undergo symmetric divisions. The induction of mitophagy, a quality control process in mitochondria, plays an essential role in self-renewing expansion of Tie2+ HSCs. Activation of the PPAR (peroxisome proliferator-activated receptor)-fatty acid oxidation pathway promotes expansion of Tie2+ HSCs through enhanced Parkin recruitment in mitochondria. These metabolic pathways are conserved in human TIE2+ HSCs. Our data thus identify mitophagy as a key mechanism of HSC expansion and suggest potential methods of cell-fate manipulation through metabolic pathways.


Subject(s)
Cell Self Renewal , Hematopoiesis/physiology , Hematopoietic Stem Cells/physiology , Mitochondria/physiology , Mitophagy/physiology , Animals , Cell Separation , Fatty Acids/metabolism , Green Fluorescent Proteins/analysis , Green Fluorescent Proteins/metabolism , Hematopoietic Stem Cells/chemistry , Metabolic Networks and Pathways , Mice , Mice, Inbred C57BL , Mitophagy/genetics , Oxidation-Reduction , Peroxisome Proliferator-Activated Receptors/metabolism , Receptor, TIE-2/analysis , Single-Cell Analysis , Ubiquitin-Protein Ligases/genetics , Ubiquitin-Protein Ligases/metabolism
7.
Sci Rep ; 6: 24303, 2016 Apr 13.
Article in English | MEDLINE | ID: mdl-27073117

ABSTRACT

Clonal heterogeneity and selection underpin many biological processes including development and tumor progression. Combinatorial fluorescent protein expression in germline cells has proven its utility for tracking the formation and regeneration of different organ systems. Such cell populations encoded by combinatorial fluorescent proteins are also attractive tools for understanding clonal expansion and clonal competition in cancer. However, the assignment of clonal identity requires an analytical framework in which clonal markings can be parameterized and validated. Here we present a systematic and quantitative method for RGB analysis of fluorescent melanoma cancer clones. We then demonstrate refined clonal trackability of melanoma cells using this scheme.


Subject(s)
Clone Cells/metabolism , Color , Luminescent Proteins/chemistry , Fluorescence
8.
Invest Ophthalmol Vis Sci ; 55(8): 5314-9, 2014 Jul 31.
Article in English | MEDLINE | ID: mdl-25082884

ABSTRACT

PURPOSE: Gamma irradiation and bone marrow transplantation (BMT) are established clinical procedures for the treatment of hematologic malignancies. The radiation targets cells in the bone marrow, but injury to other tissues, including the central nervous system (CNS), have been reported. Here, we examine if anti-inflammatory treatment can mitigate the radiation-induced turnover of retinal microglia and the replacement by bone marrow-derived cells (BMDCs). METHODS: Two-color chimeric mice were generated by lethal irradiation of heterozygous CX3CR1-GFP mice that express GFP in microglial cells and bone marrow transplantation from universal DsRed donor mice. Mice were treated with the corticosteroid dexamethasone; a control group received no dexamethasone treatment. The populations of resident microglia (GFP+) and BMDCs (DsRed+) were quantified by serial in vivo imaging for 10 weeks after irradiation with a confocal scanning laser ophthalmoscope that we custom-built specifically for multicolor imaging of the murine retina. RESULTS: Ionizing radiation resulted in loss of 75% of the resident retinal microglia population after 70 days. Recruitment of BMDCs was delayed with respect to the microglia loss, resulting in a transient depletion of the total immune cell number in the retina. With dexamethasone treatment, both the loss of the resident microglia and the infiltration of BMDCs were suppressed by at least 50%. CONCLUSIONS: Anti-inflammatory treatment with the corticosteroidal agent dexamethasone preserves resident microglia and minimizes recruitment of BMDCs after ionizing radiation exposure and BMT.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Dexamethasone/pharmacology , Microglia/drug effects , Microglia/radiation effects , Retina , Animals , Bone Marrow Cells/drug effects , Bone Marrow Cells/pathology , Bone Marrow Cells/radiation effects , Disease Models, Animal , Green Fluorescent Proteins/metabolism , Mice , Mice, Transgenic , Microglia/metabolism , Retina/drug effects , Retina/radiation effects
9.
Methods Mol Biol ; 1185: 247-65, 2014.
Article in English | MEDLINE | ID: mdl-25062634

ABSTRACT

Over the past 50 years, much insight has been gained into the biology of hematopoietic stem cells (HSCs). Much of this information has been gained though isolation of specific bone marrow populations, and transplantation into irradiated recipients followed by characterization of chimeras months later. These studies have yielded insights into the function of HSCs, but have shed little light on the interactions of individual stem cells with their environment. Characterization of the behavior of single HSCs awaited the use of relatively noninvasive intravital microscopy, which allows one to identify rare cells in real time and follow them in multiple imaging sessions. Here we describe techniques used to image transplanted HSCs in the mouse calvarium using hybrid confocal/multi-photon microscopy and second harmonic imaging. For detection, fluorescently tagged HSCs are transplanted into a recipient mouse. The architecture of the bone marrow can be delineated using a combination of fluorescent probes and vascular dyes, second harmonic generation to detect the collagen signal from bone, and transgenic recipient mice containing specific fluorescent support cell populations.


Subject(s)
Hematopoietic Stem Cells/cytology , Molecular Imaging/methods , Skull/cytology , Animals , Bone Marrow Cells/cytology , Bone Marrow Transplantation , Imaging, Three-Dimensional , Mice , Microscopy, Fluorescence
10.
Nature ; 508(7495): 269-73, 2014 Apr 10.
Article in English | MEDLINE | ID: mdl-24590072

ABSTRACT

Characterization of how the microenvironment, or niche, regulates stem cell activity is central to understanding stem cell biology and to developing strategies for the therapeutic manipulation of stem cells. Low oxygen tension (hypoxia) is commonly thought to be a shared niche characteristic in maintaining quiescence in multiple stem cell types. However, support for the existence of a hypoxic niche has largely come from indirect evidence such as proteomic analysis, expression of hypoxia inducible factor-1α (Hif-1α) and related genes, and staining with surrogate hypoxic markers (for example, pimonidazole). Here we perform direct in vivo measurements of local oxygen tension (pO2) in the bone marrow of live mice. Using two-photon phosphorescence lifetime microscopy, we determined the absolute pO2 of the bone marrow to be quite low (<32 mm Hg) despite very high vascular density. We further uncovered heterogeneities in local pO2, with the lowest pO2 (∼9.9 mm Hg, or 1.3%) found in deeper peri-sinusoidal regions. The endosteal region, by contrast, is less hypoxic as it is perfused with small arteries that are often positive for the marker nestin. These pO2 values change markedly after radiation and chemotherapy, pointing to the role of stress in altering the stem cell metabolic microenvironment.


Subject(s)
Bone Marrow/metabolism , Oxygen/analysis , Animals , Arteries/metabolism , Bone Marrow/blood supply , Bone Marrow/drug effects , Bone Marrow/radiation effects , Busulfan/pharmacology , Cell Hypoxia , Hematopoietic Stem Cells/cytology , Hematopoietic Stem Cells/metabolism , Hypoxia/diagnosis , Hypoxia/metabolism , Luminescent Measurements , Male , Mice , Mice, Inbred C57BL , Microscopy , Nestin/metabolism , Oxygen/metabolism , Photons , Stem Cell Niche/drug effects , Stem Cell Niche/radiation effects
11.
PLoS One ; 8(8): e69257, 2013.
Article in English | MEDLINE | ID: mdl-23990881

ABSTRACT

We describe a novel photoconversion technique to track individual cells in vivo using a commercial lipophilic membrane dye, DiR. We show that DiR exhibits a permanent fluorescence emission shift (photoconversion) after light exposure and does not reacquire the original color over time. Ratiometric imaging can be used to distinguish photoconverted from non-converted cells with high sensitivity. Combining the use of this photoconvertible dye with intravital microscopy, we tracked the division of individual hematopoietic stem/progenitor cells within the calvarium bone marrow of live mice. We also studied the peripheral differentiation of individual T cells by tracking the gain or loss of FoxP3-GFP expression, a marker of the immune suppressive function of CD4(+) T cells. With the near-infrared photoconvertible membrane dye, the entire visible spectral range is available for simultaneous use with other fluorescent proteins to monitor gene expression or to trace cell lineage commitment in vivo with high spatial and temporal resolution.


Subject(s)
Cell Membrane/metabolism , Coloring Agents/chemistry , Photochemistry , Single-Cell Analysis/methods , Animals , Bone Marrow/metabolism , CD4-Positive T-Lymphocytes/cytology , Cell Differentiation , Cell Lineage , Forkhead Transcription Factors/metabolism , Green Fluorescent Proteins/metabolism , Hematopoietic Stem Cells/cytology , Luminescent Proteins/metabolism , Mice , Mice, Inbred C57BL , Mice, Transgenic , Microscopy, Confocal , Spectrometry, Fluorescence , Staining and Labeling/methods , Stem Cells/cytology , T-Lymphocytes/cytology , Time Factors
12.
Cytometry A ; 79(10): 758-65, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21905206

ABSTRACT

We provide an overview of the methods used to label circulating cells for fluorescence detection by in vivo flow cytometry. These methods are useful for cell tracking in small animals without the need to draw blood samples and are particularly useful for the detection of circulating cancer cells and quantification of circulating immune cells.


Subject(s)
Antibodies/analysis , Flow Cytometry , Fluorescent Dyes/analysis , Green Fluorescent Proteins/analysis , Neoplasms/diagnosis , Neoplastic Cells, Circulating/pathology , Staining and Labeling , Adoptive Transfer , Animals , Antibodies/metabolism , Cell Line, Tumor , Flow Cytometry/methods , Fluorescence , Fluorescent Dyes/chemistry , Green Fluorescent Proteins/chemistry , Humans , Mice , Molecular Imaging/methods , Neoplasms/pathology , Photoacoustic Techniques/methods , Staining and Labeling/methods
13.
J Biomed Opt ; 16(1): 011006, 2011.
Article in English | MEDLINE | ID: mdl-21280893

ABSTRACT

Multiple myeloma (MM), the second most common hematological malignancy, initiates from a single site and spreads via circulation to multiple sites in the bone marrow (BM). Methods to track MM cells both in the BM and circulation would be useful for developing new therapeutic strategies to target MM cell spread. We describe the use of complementary optical techniques to track human MM cells expressing both bioluminescent and fluorescent reporters in a mouse xenograft model. Long-term tumor growth and response to therapy are monitored using bioluminescence imaging (BLI), while numbers of circulating tumor cells are detected by in-vivo flow cytometry. Intravital microscopy is used to detect early seeding of MM cells to the BM, as well as residual cancer cells that remain in the BM after the bulk of the tumor is eradicated following drug treatment. Thus, intravital microscopy provides a powerful, albeit invasive, means to study cellular processes in vivo at the very early stage of the disease process and at the very late stage of therapeutic intervention when the tumor burden is too small to be detected by other imaging methods.


Subject(s)
Boronic Acids/therapeutic use , Cell Tracking/methods , Flow Cytometry/methods , Microscopy, Fluorescence/methods , Multiple Myeloma/drug therapy , Multiple Myeloma/physiopathology , Pyrazines/therapeutic use , Animals , Antineoplastic Agents/therapeutic use , Bortezomib , Cell Line, Tumor , Female , Male , Mice , Mice, Inbred BALB C , Mice, SCID , Multiple Myeloma/pathology , Treatment Outcome
14.
Opt Express ; 18(2): 988-99, 2010 Jan 18.
Article in English | MEDLINE | ID: mdl-20173920

ABSTRACT

We describe a new method for imaging leukocytes in vivo by exciting the endogenous protein fluorescence in the ultraviolet (UV) spectral region where tryptophan is the major fluorophore. Two-photon excitation near 590 nm allows noninvasive optical sectioning through the epidermal cell layers into the dermis of mouse skin, where leukocytes can be observed by video-rate microscopy to interact dynamically with the dermal vascular endothelium. Inflammation significantly enhances leukocyte rolling, adhesion, and tissue infiltration. After exiting the vasculature, leukocytes continue to move actively in tissue as observed by time-lapse microscopy, and are distinguishable from resident autofluorescent cells that are not motile. Because the new method alleviates the need to introduce exogenous labels, it is potentially applicable for tracking leukocytes and monitoring inflammatory cellular reactions in humans.


Subject(s)
Leukocytes/cytology , Leukocytes/physiology , Luminescent Proteins/analysis , Microscopy, Fluorescence, Multiphoton/methods , Skin/cytology , Tryptophan/analysis , Animals , Cell Movement , Cells, Cultured , Mice , Mice, Inbred BALB C , Skin/blood supply
15.
Blood ; 114(3): 619-29, 2009 Jul 16.
Article in English | MEDLINE | ID: mdl-19443661

ABSTRACT

The interaction of multiple myeloma (MM) cells with the bone marrow (BM) milieu plays a crucial role in MM pathogenesis. Stromal cell-derived factor-1 (SDF1) regulates homing of MM cells to the BM. In this study, we examined the role of RhoA and Rac1 GTPases in SDF1-induced adhesion and chemotaxis of MM. We found that both RhoA and Rac1 play key roles in SDF1-induced adhesion of MM cells to BM stromal cells, whereas RhoA was involved in chemotaxis and motility. Furthermore, both ROCK and Rac1 inhibitors reduced SDF1-induced polymerization of actin and activation of LIMK, SRC, FAK, and cofilin. Moreover, RhoA and Rac1 reduced homing of MM cells to BM niches. In conclusion, we characterized the role of RhoA and Rac1 GTPases in SDF1-induced adhesion, chemotaxis, and homing of MM cells to the BM, providing the framework for targeting RhoA and Rac1 GTPases as novel MM therapy.


Subject(s)
Cell Adhesion , Chemokine CXCL12/physiology , Chemotaxis , Multiple Myeloma/pathology , rac1 GTP-Binding Protein/physiology , rhoA GTP-Binding Protein/physiology , Animals , Bone Marrow , Cytoskeletal Proteins/metabolism , Humans , Mice , Mice, SCID , Stromal Cells , Tumor Cells, Cultured
16.
Blood ; 113(18): 4341-51, 2009 Apr 30.
Article in English | MEDLINE | ID: mdl-19139079

ABSTRACT

The interaction of multiple myeloma (MM) cells with their microenvironment in the bone marrow (BM) provides a protective environment and resistance to therapeutic agents. We hypothesized that disruption of the interaction of MM cells with their BM milieu would lead to their sensitization to therapeutic agents such as bortezomib, melphalan, doxorubicin, and dexamethasone. We report that the CXCR4 inhibitor AMD3100 induces disruption of the interaction of MM cells with the BM reflected by mobilization of MM cells into the circulation in vivo, with kinetics that differed from that of hematopoietic stem cells. AMD3100 enhanced sensitivity of MM cell to multiple therapeutic agents in vitro by disrupting adhesion of MM cells to bone marrow stromal cells (BMSCs). Moreover, AMD3100 increased mobilization of MM cells to the circulation in vivo, increased the ratio of apoptotic circulating MM cells, and enhanced the tumor reduction induced by bortezomib. Mechanistically, AMD3100 significantly inhibited Akt phosphorylation and enhanced poly(ADP-ribose) polymerase (PARP) cleavage as a result of bortezomib, in the presence of BMSCs in coculture. These experiments provide a proof of concept for the use of agents that disrupt interaction with the microenvironment for enhancement of efficacy of cytotoxic agents in cancer therapy.


Subject(s)
Anti-HIV Agents/pharmacology , Antineoplastic Agents/pharmacology , Bone Marrow/metabolism , Heterocyclic Compounds/pharmacology , Multiple Myeloma/drug therapy , Multiple Myeloma/metabolism , Receptors, CXCR4/antagonists & inhibitors , Animals , Apoptosis/drug effects , Benzylamines , Boronic Acids/pharmacology , Bortezomib , Cell Adhesion/drug effects , Cell Movement/physiology , Cell Survival/drug effects , Coculture Techniques , Colony-Forming Units Assay , Cyclams , Drug Resistance, Neoplasm , Fibronectins/metabolism , Flow Cytometry , Humans , Immunoblotting , Immunoenzyme Techniques , Integrin alpha4beta1/genetics , Integrin alpha4beta1/metabolism , Intercellular Adhesion Molecule-1/genetics , Intercellular Adhesion Molecule-1/metabolism , Lentivirus/genetics , Male , Mice , Mice, SCID , Pyrazines/pharmacology , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/pharmacology , Stromal Cells/metabolism , Transfection , Tumor Cells, Cultured , Xenograft Model Antitumor Assays
17.
Mol Imaging ; 5(1): 31-40, 2006.
Article in English | MEDLINE | ID: mdl-16779968

ABSTRACT

Molecular expression on the vascular endothelium is critical in regulating the interaction of circulating cells with the blood vessel wall. Leukocytes as well as circulating cancer cells gain entry into tissue by interacting with adhesion molecules on the endothelial cells (EC). Molecular targets on the EC are increasingly being explored for tissue-specific delivery of therapeutic and imaging agents. Here we use in vivo immunofluorescence microscopy to visualize the endothelial molecular expression in the vasculature of live animals. High-resolution images are obtained by optical sectioning through the intact skin using in vivo confocal and multiphoton microscopy after in situ labeling of EC surface markers with fluorescent antibodies. Other vascular beds such as the bone marrow and ocular blood vessels can be imaged with little or no tissue manipulation. Live imaging is particularly useful for following the dynamic expression of inducible molecules such as E-selectin during an inflammatory response.


Subject(s)
Cell Adhesion Molecules/analysis , Endothelial Cells/chemistry , Selectins/analysis , Animals , Cell Adhesion , Cell Adhesion Molecules/metabolism , E-Selectin/analysis , E-Selectin/genetics , E-Selectin/metabolism , Endothelial Cells/cytology , Endothelial Cells/metabolism , Endothelium, Vascular/chemistry , Endothelium, Vascular/cytology , Endothelium, Vascular/metabolism , Eye/chemistry , Eye/metabolism , Female , Leukocytes , Mice , Mice, Inbred BALB C , Mice, Knockout , Microscopy, Confocal , Microscopy, Fluorescence , P-Selectin/analysis , P-Selectin/metabolism , Platelet Endothelial Cell Adhesion Molecule-1/analysis , Platelet Endothelial Cell Adhesion Molecule-1/metabolism , Selectins/metabolism , Skin/chemistry , Skin/metabolism
18.
Nature ; 435(7044): 969-73, 2005 Jun 16.
Article in English | MEDLINE | ID: mdl-15959517

ABSTRACT

The organization of cellular niches is known to have a key role in regulating normal stem cell differentiation and regeneration, but relatively little is known about the architecture of microenvironments that support malignant metastasis. Using dynamic in vivo confocal imaging, here we show that murine bone marrow contains unique anatomic regions defined by specialized endothelium. This vasculature expresses the adhesion molecule E-selectin and the chemoattractant stromal-cell-derived factor 1 (SDF-1) in discrete, discontinuous areas that influence the homing of a variety of tumour cell lines. Disruption of the interactions between SDF-1 and its receptor CXCR4 inhibits the homing of Nalm-6 cells (an acute lymphoblastic leukaemia cell line) to these vessels. Further studies revealed that circulating leukaemic cells can engraft around these vessels, suggesting that this molecularly distinct vasculature demarcates a microenvironment for early metastatic tumour spread in bone marrow. Finally, purified haematopoietic stem/progenitor cells and lymphocytes also localize to the same microdomains, indicating that this vasculature might also function in benign states to demarcate specific portals for the entry of cells into the marrow space. Specialized vascular structures therefore appear to delineate a microenvironment with unique physiology that can be exploited by circulating malignant cells.


Subject(s)
Bone Marrow Cells/cytology , Endothelial Cells/cytology , Endothelial Cells/metabolism , Microscopy, Confocal/methods , Neoplasms/pathology , Animals , Bone Marrow Cells/metabolism , Cell Adhesion , Cell Line, Tumor , Cell Movement , Cytokines/metabolism , E-Selectin/metabolism , Leukemia/metabolism , Leukemia/pathology , Mice , Mice, Inbred BALB C , Mice, SCID , Receptors, CXCR4/metabolism , Skull/cytology
19.
Invest Ophthalmol Vis Sci ; 44(10): 4489-96, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14507897

ABSTRACT

PURPOSE: Hyperfluorescent cells labeled with indocyanine green (ICG) have been observed in retinal and choroidal circulation using scanning laser ophthalmoscopy. It has been suggested that ICG labels leukocytes and that ICG can be used to track leukocyte movement in vivo. The purpose of this study is to identify the cell population that takes up ICG and to study their trafficking pattern in vivo by confocal fluorescence microscopy. METHODS: ICG was injected into the mouse tail vein, and images were taken by in vivo confocal microscopy. The trafficking pattern of ICG-labeled cells was compared with that of rhodamine 6G-labeled leukocytes. In vitro labeling of human blood cells with antibodies against cell lineage markers and with DNA stains was further used to identify the ICG-labeled cells. Antibodies against the following cell surface markers were used: CD45 (leukocytes), CD3 (T lymphocytes), CD19 (B lymphocytes), CD16 (Fc receptor), glycophorin A (erythroid lineage cells), and CD71 (transferrin receptor). RESULTS: The ICG-labeled cells were made up of two blood cell populations with distinct levels of ICG uptake. The strongly ICG-labeled cells did not roll on dermal vascular endothelium in vivo, in contrast to rhodamine 6G-labeled leukocytes. They were identified as reticulocytes because antibody staining showed that they were CD 45(-), glycophorin A(+) and CD 71(+). The weakly ICG-labeled cells were identified as neutrophils because they were CD45(+), CD16(+), CD3(-), and CD19(-). CONCLUSIONS: ICG strongly labels reticulocytes and weakly labels neutrophils. To the authors' knowledge, this is the first report of selective staining of reticulocytes by ICG.


Subject(s)
Coloring Agents/pharmacokinetics , Indocyanine Green/pharmacokinetics , Reticulocytes/metabolism , Animals , Blood Circulation , Chemotaxis, Leukocyte , Female , Mice , Mice, Inbred BALB C , Microscopy, Confocal , Neutrophils/metabolism , Reticulocytes/cytology , Rhodamines/pharmacokinetics , Staining and Labeling
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