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  1. Article ; Online: Non-invasive optical imaging of the lymphatic vasculature of a mouse.

    Robinson, Holly A / Kwon, SunKuk / Hall, Mary A / Rasmussen, John C / Aldrich, Melissa B / Sevick-Muraca, Eva M

    Journal of visualized experiments : JoVE

    2013  , Issue 73, Page(s) e4326

    Abstract: The lymphatic vascular system is an important component of the circulatory system that maintains fluid homeostasis, provides immune surveillance, and mediates fat absorption in the gut. Yet despite its critical function, there is comparatively little ... ...

    Abstract The lymphatic vascular system is an important component of the circulatory system that maintains fluid homeostasis, provides immune surveillance, and mediates fat absorption in the gut. Yet despite its critical function, there is comparatively little understanding of how the lymphatic system adapts to serve these functions in health and disease. Recently, we have demonstrated the ability to dynamically image lymphatic architecture and lymph "pumping" action in normal human subjects as well as in persons suffering lymphatic dysfunction using trace administration of a near-infrared fluorescent (NIRF) dye and a custom, Gen III-intensified imaging system. NIRF imaging showed dramatic changes in lymphatic architecture and function with human disease. It remains unclear how these changes occur and new animal models are being developed to elucidate their genetic and molecular basis. In this protocol, we present NIRF lymphatic, small animal imaging using indocyanine green (ICG), a dye that has been used for 50 years in humans, and a NIRF dye-labeled cyclic albumin binding domain (cABD-IRDye800) peptide that preferentially binds mouse and human albumin. Approximately 5.5 times brighter than ICG, cABD-IRDye800 has a similar lymphatic clearance profile and can be injected in smaller doses than ICG to achieve sufficient NIRF signals for imaging. Because both cABD-IRDye800 and ICG bind to albumin in the interstitial space, they both may depict active protein transport into and within the lymphatics. Intradermal (ID) injections (5-50 μl) of ICG (645 μM) or cABD-IRDye800 (200 μM) in saline are administered to the dorsal aspect of each hind paw and/or the left and right side of the base of the tail of an isoflurane-anesthetized mouse. The resulting dye concentration in the animal is 83-1,250 μg/kg for ICG or 113-1,700 μg/kg for cABD-IRDye800. Immediately following injections, functional lymphatic imaging is conducted for up to 1 hr using a customized, small animal NIRF imaging system. Whole animal spatial resolution can depict fluorescent lymphatic vessels of 100 microns or less, and images of structures up to 3 cm in depth can be acquired. Images are acquired using V++ software and analyzed using ImageJ or MATLAB software. During analysis, consecutive regions of interest (ROIs) encompassing the entire vessel diameter are drawn along a given lymph vessel. The dimensions for each ROI are kept constant for a given vessel and NIRF intensity is measured for each ROI to quantitatively assess "packets" of lymph moving through vessels.
    MeSH term(s) Animals ; Coloring Agents/chemistry ; Indocyanine Green/chemistry ; Indoles/chemistry ; Lymphatic Vessels/anatomy & histology ; Lymphatic Vessels/chemistry ; Mice ; Optical Imaging/methods
    Chemical Substances Coloring Agents ; IRDye800 ; Indoles ; Indocyanine Green (IX6J1063HV)
    Language English
    Publishing date 2013-03-08
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Video-Audio Media
    ZDB-ID 2259946-0
    ISSN 1940-087X ; 1940-087X
    ISSN (online) 1940-087X
    ISSN 1940-087X
    DOI 10.3791/4326
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Non-invasive optical imaging of the lymphatic vasculature of a mouse

    Robinson, Holly A / Kwon, SunKuk / Hall, Mary A / Rasmussen, John C / Aldrich, Melissa B / Sevick-Muraca, Eva M

    Journal of visualized experiments. 2013 Mar. 08, , no. 73

    2013  

    Abstract: The lymphatic vascular system is an important component of the circulatory system that maintains fluid homeostasis, provides immune surveillance, and mediates fat absorption in the gut. Yet despite its critical function, there is comparatively little ... ...

    Abstract The lymphatic vascular system is an important component of the circulatory system that maintains fluid homeostasis, provides immune surveillance, and mediates fat absorption in the gut. Yet despite its critical function, there is comparatively little understanding of how the lymphatic system adapts to serve these functions in health and disease1. Recently, we have demonstrated the ability to dynamically image lymphatic architecture and lymph "pumping" action in normal human subjects as well as in persons suffering lymphatic dysfunction using trace administration of a near-infrared fluorescent (NIRF) dye and a custom, Gen III-intensified imaging system2-4. NIRF imaging showed dramatic changes in lymphatic architecture and function with human disease. It remains unclear how these changes occur and new animal models are being developed to elucidate their genetic and molecular basis. In this protocol, we present NIRF lymphatic, small animal imaging5,6 using indocyanine green (ICG), a dye that has been used for 50 years in humans7, and a NIRF dye-labeled cyclic albumin binding domain (cABD-IRDye800) peptide that preferentially binds mouse and human albumin8. Approximately 5.5 times brighter than ICG, cABD-IRDye800 has a similar lymphatic clearance profile and can be injected in smaller doses than ICG to achieve sufficient NIRF signals for imaging8. Because both cABD-IRDye800 and ICG bind to albumin in the interstitial space8, they both may depict active protein transport into and within the lymphatics. Intradermal (ID) injections (5-50 μl) of ICG (645 μM) or cABD-IRDye800 (200 μM) in saline are administered to the dorsal aspect of each hind paw and/or the left and right side of the base of the tail of an isoflurane-anesthetized mouse. The resulting dye concentration in the animal is 83-1,250 μg/kg for ICG or 113-1,700 μg/kg for cABD-IRDye800. Immediately following injections, functional lymphatic imaging is conducted for up to 1 hr using a customized, small animal NIRF imaging system. Whole animal spatial resolution can depict fluorescent lymphatic vessels of 100 microns or less, and images of structures up to 3 cm in depth can be acquired9. Images are acquired using V++ software and analyzed using ImageJ or MATLAB software. During analysis, consecutive regions of interest (ROIs) encompassing the entire vessel diameter are drawn along a given lymph vessel. The dimensions for each ROI are kept constant for a given vessel and NIRF intensity is measured for each ROI to quantitatively assess "packets" of lymph moving through vessels.
    Keywords absorption ; albumins ; animal models ; computer software ; digestive system ; dyes ; fluorescence ; homeostasis ; human diseases ; image analysis ; lipids ; lymph ; mice ; monitoring ; peptides ; tail
    Language English
    Dates of publication 2013-0308
    Size p. e4326.
    Publishing place Journal of Visualized Experiments
    Document type Article
    ZDB-ID 2259946-0
    ISSN 1940-087X
    ISSN 1940-087X
    DOI 10.3791/4326
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Matrix metalloproteinase-9 is a diagnostic marker of heterotopic ossification in a murine model.

    Rodenberg, Eric / Azhdarinia, Ali / Lazard, ZaWaunyka W / Hall, Mary / Kwon, Sun Kuk / Wilganowski, Nathaniel / Salisbury, Elizabeth A / Merched-Sauvage, Maria / Olmsted-Davis, Elizabeth A / Sevick-Muraca, Eva M / Davis, Alan R

    Tissue engineering. Part A

    2011  Volume 17, Issue 19-20, Page(s) 2487–2496

    Abstract: Heterotopic ossification (HO) is a serious disorder that occurs when there is aberrant bone morphogenic protein (BMP) signaling in soft tissues. Currently, there are no methods to detect HO before mineralization occurs. Yet once mineralization occurs, ... ...

    Abstract Heterotopic ossification (HO) is a serious disorder that occurs when there is aberrant bone morphogenic protein (BMP) signaling in soft tissues. Currently, there are no methods to detect HO before mineralization occurs. Yet once mineralization occurs, there are no effective treatments, short of surgery, to reverse HO. Herein, we used in vivo molecular imaging and confirmatory ex vivo tissue analyses of an established murine animal model of BMP-induced HO to show that matrix metalloproteinase-9 (MMP-9) can be detected as an early-stage biomarker before mineralization. Ex vivo analyses show that active MMP-9 protein is significantly elevated within tissues undergoing HO as early as 48 h after BMP induction, with its expression co-localizing to nerves and vessels. In vivo molecular imaging with a dual-labeled near-infrared fluorescence and micro-positron emission tomography (μPET) agent specific to MMP-2/-9 expression paralleled the ex vivo observations and reflected the site of HO formation as detected from microcomputed tomography 7 days later. The results suggest that the MMP-9 is a biomarker of the early extracellular matrix (ECM) re-organization and could be used as an in vivo diagnostic with confirmatory ex vivo tissue analysis for detecting HO or conversely for monitoring the success of tissue-engineered bone implants that employ ECM biology for engraftment.
    MeSH term(s) Amino Acid Sequence ; Animals ; Biomarkers/metabolism ; Disease Models, Animal ; Fluorescent Antibody Technique ; Gene Expression Regulation, Enzymologic/drug effects ; Hindlimb/drug effects ; Hindlimb/pathology ; Humans ; Matrix Metalloproteinase 2/metabolism ; Matrix Metalloproteinase 9/genetics ; Matrix Metalloproteinase 9/metabolism ; Mice ; Molecular Imaging ; Molecular Sequence Data ; Multimodal Imaging ; Ossification, Heterotopic/diagnosis ; Ossification, Heterotopic/enzymology ; Peptides, Cyclic/chemistry ; Peptides, Cyclic/pharmacology ; Positron-Emission Tomography ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Spectroscopy, Near-Infrared ; Tomography, X-Ray Computed
    Chemical Substances Biomarkers ; Peptides, Cyclic ; RNA, Messenger ; Matrix Metalloproteinase 2 (EC 3.4.24.24) ; Matrix Metalloproteinase 9 (EC 3.4.24.35) ; Mmp9 protein, mouse (EC 3.4.24.35)
    Language English
    Publishing date 2011-10
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2420582-5
    ISSN 1937-335X ; 1937-3341
    ISSN (online) 1937-335X
    ISSN 1937-3341
    DOI 10.1089/ten.TEA.2011.0007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Hydrogel microsphere encapsulation of a cell-based gene therapy system increases cell survival of injected cells, transgene expression, and bone volume in a model of heterotopic ossification.

    Olabisi, Ronke M / Lazard, Zawaunyka W / Franco, Christy L / Hall, Mary A / Kwon, Sun Kuk / Sevick-Muraca, Eva M / Hipp, John A / Davis, Alan R / Olmsted-Davis, Elizabeth A / West, Jennifer L

    Tissue engineering. Part A

    2010  Volume 16, Issue 12, Page(s) 3727–3736

    Abstract: Bone morphogenetic proteins (BMPs) are well known for their osteoinductive activity, yet harnessing this capacity remains a high-priority research focus. We present a novel technology that delivers high BMP-2 levels at targeted locations for rapid ... ...

    Abstract Bone morphogenetic proteins (BMPs) are well known for their osteoinductive activity, yet harnessing this capacity remains a high-priority research focus. We present a novel technology that delivers high BMP-2 levels at targeted locations for rapid endochondral bone formation, enhancing our preexisting cell-based gene therapy system by microencapsulating adenovirus-transduced cells in nondegradable poly(ethylene glycol) diacrylate (PEGDA) hydrogels before intramuscular delivery. This study evaluates the in vitro and in vivo viability, gene expression, and bone formation from transgenic fibroblasts encapsulated in PEGDA microspheres. Fluorescent viability and cytotoxicity assays demonstrated >95% viability in microencapsulated cells. ELISA and alkaline phosphatase assays established that BMP-2 secretion and specific activity from microencapsulated AdBMP2-transduced fibroblasts were not statistically different from monolayer. Longitudinal transgene expression studies of AdDsRed-transduced fibroblasts, followed through live animal optical fluorescent imaging, showed that microencapsulated cells expressed longer than unencapsulated cells. When comparable numbers of microencapsulated AdBMP2-transduced cells were intramuscularly injected into mice, microcomputed tomography evaluation demonstrated that the resultant heterotopic bone formation was approximately twice the volume of unencapsulated cells. The data suggest that microencapsulation protects cells and prolongs and spatially distributes transgene expression. Thus, incorporation of PEGDA hydrogels significantly advances current gene therapy bone repair approaches.
    MeSH term(s) Alkaline Phosphatase/metabolism ; Animals ; Bone Morphogenetic Protein 2/genetics ; Bone Morphogenetic Protein 2/metabolism ; Cell Line ; Cell Survival/genetics ; Cell Survival/physiology ; Enzyme-Linked Immunosorbent Assay ; Female ; Fibroblasts/cytology ; Fibroblasts/metabolism ; Humans ; Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry ; Mice ; Mice, SCID ; Microspheres ; Tissue Engineering/methods ; Transgenes/genetics ; Transgenes/physiology ; X-Ray Microtomography
    Chemical Substances BMP2 protein, human ; Bone Morphogenetic Protein 2 ; Hydrogel, Polyethylene Glycol Dimethacrylate (25852-47-5) ; Alkaline Phosphatase (EC 3.1.3.1)
    Language English
    Publishing date 2010-09-01
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2420582-5
    ISSN 1937-335X ; 1937-3341
    ISSN (online) 1937-335X
    ISSN 1937-3341
    DOI 10.1089/ten.TEA.2010.0234
    Database MEDical Literature Analysis and Retrieval System OnLINE

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