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Development (Cambridge, England) 2005, 132:5199-209.\\\",\\\"@context\\\":\\\"http://schema.org\\\"}\"}],\"sdlPageMetaData\":{\"tcmId\":\"tcm:506-363053-64\",\"lastPublishedDate\":\"2020-10-07T15:12:01.6919101-04:00\",\"revisionDate\":\"2019-07-15T08:40:02\",\"version\":1},\"publicationUrl\":\"/intmed/cardio/ycvrc\",\"topBanner\":null,\"mainComponents\":[{\"key\":\"ProfileDetails\",\"orderOnPage\":0,\"model\":{\"mainInfo\":{\"fullName\":\"Suk-Won Jin\",\"suffixes\":{\"familySuffix\":null,\"nonFamilySuffixes\":[\"PhD\"]},\"titles\":[],\"image\":null,\"editUrl\":\"https://prod.admin.profile.yale.edu/Profiles/76729/GeneralInfo/Edit\"},\"contacts\":{\"fullName\":\"Suk-Won Jin\",\"cvUrl\":\"https://prod.admin.profile.yale.edu/Profiles/Cv/user/suk-won_jin\",\"generalContacts\":{\"email\":\"suk-won.jin@yale.edu\",\"academicPhone\":null,\"officeFax\":null,\"clinicPhone\":null,\"clinicFax\":null,\"labPhone\":null},\"externalProfileLink\":null,\"locations\":{\"patientCareLocations\":[],\"officeLocations\":[{\"address\":{\"id\":348,\"officeName\":null,\"name\":null,\"addressLine1\":\"300 George Street\",\"addressLine2\":\"Ste 770G\",\"city\":\"New Haven\",\"region\":\"CT\",\"country\":\"United States\",\"postalCode\":\"06511\"},\"url\":\"/intmed/cardio/ycvrc/profile/suk-won_jin/?tab=location&locationId=924\",\"phones\":[]}],\"labLocations\":[]},\"mailingAddresses\":[],\"suffixes\":{\"familySuffix\":null,\"nonFamilySuffixes\":[\"PhD\"]},\"labLinks\":[],\"relatedLinks\":[],\"ymProfileUrl\":null},\"bioTab\":{\"biography\":null,\"photo\":null,\"gallery\":null,\"organizations\":[{\"id\":109148,\"name\":\"Cardiovascular Medicine\",\"url\":\"https://medicine.yale.edu/intmed/cardio\"},{\"id\":108789,\"name\":\"Internal Medicine\",\"url\":\"https://medicine.yale.edu/intmed/\"},{\"id\":114820,\"name\":\"Office of Cooperative Research\",\"url\":\"http://ocr.yale.edu/\"},{\"id\":109701,\"name\":\"Vascular Biology and Therapeutics Program\",\"url\":\"https://medicine.yale.edu/vbt/\"},{\"id\":113853,\"name\":\"Yale Cardiovascular Research Center\",\"url\":\"https://medicine.yale.edu/intmed/cardio/ycvrc/\"},{\"id\":110762,\"name\":\"Yale University\",\"url\":\"https://www.yale.edu/\"}],\"appointmentOrganizations\":[{\"id\":109148,\"name\":\"Cardiovascular Medicine\",\"url\":\"https://medicine.yale.edu/intmed/cardio\"}],\"educations\":[{\"degree\":\"PhD\",\"institution\":\"University of Michigan/Ann Arbor (2000)\"},{\"degree\":\"MS\",\"institution\":\"Yonsei University (1995)\"},{\"degree\":\"BS\",\"institution\":\"Yonsei University (1993)\"},{\"degree\":\"Post-doctoral fellow\",\"institution\":\"UCSF\"}],\"honors\":[],\"services\":[],\"activities\":[]},\"researchTab\":{\"research\":{\"description\":\"\\n\\n1. Analyzing the\\nfunction of Bone Morphogenetic Protein (BMP) signaling during vascular patterning:\\n\\nDuring zebrafish development, angiogenesis expands the axial\\nvessels into a complex vascular network that is necessary for efficient oxygen\\ndelivery. Although the axial artery (dorsal aorta) and the axial vein are\\nspatially juxtaposed, the initial angiogenic sprouts from these vessels extend in opposite\\ndirections, suggesting that distinct cues may regulate angiogenesis of\\nthe axial vessels. We have recently found\\nthat angiogenic sprouts from the dorsal aorta are dependent on Vegf-A signaling, and do not respond to Bmp\\nsignals. In contrast, sprouts from the\\naxial vein are regulated by Bmp signaling independent of Vegf-A signals, suggesting that Bmp is a\\nvein-specific angiogenic cue during early vascular development (Wiley et al, in\\npress). Our results support a paradigm, whereby different signals\\nregulate distinct programs of sprouting angiogenesis from the axial vein and\\nartery, and suggest that signaling heterogeneity contributes to the complexity\\nof vascular networks. We are currently investigating 1) how venous but not\\narterial endothelial cells respond to Bmp signaling, 2) what are the roles of\\nBmp signaling in lymphatic development, and 3) how Bmp signaling is transduced\\nwithin endothelial cells.\\n\\n \\n
\\n2. Investigating\\ninteraction between endothelial and hematopoietic lineages during development:\\n\\nIt has been hypothesized that endothelial and hematopoietic lineages are\\nclosely related during development. For instance, these two lineages share\\ncommon precursor population, the hemangioblasts. Using the combination of\\nsingle cell labeling and lineage tracing, we have shown that the hemangioblasts\\nexist during development (Vogeli et al, 2006). We have also shown that Notch\\nsignaling is essential in modulating the number of the endothelial progenitors.\\nInhibition of Notch signaling increases the number of endothelial cells by\\nthree folds at the expense of hematopoietic stem cells, suggesting that Notch\\nsignaling pathway promote hematopoietic stem cell fate over endothelial cell\\nfate in early development (Lee et al, 2009). Later in development, we have\\nrecently made an observation that both arterial and venous endothelial cells\\nare capable of generating cmyb\\npositive hematopoietic stem cells, presumably via asymmetric cell division. To\\nbetter understand how the endothelial lineage contributes to the hematopoietic\\nlineage later in development, we are currently\\ninvestigating 1) how asymmetric cell division might regulate the number of\\nhematopoietic stem cells, 2) how plane of cell division regulates the emergence\\nof hematopoietic stem cells from the endothelial cells, and 3) what are the\\nroles of environmental factors such as hemodynamic forces on the formation of\\nhematopoietic stem cells from the endothelial lineage.\\n\\n \\n
\\n3. Analyzing molecular and cellular defects of vascular specific mutations:\\n\\nFrom recently completed screen, several mutations affecting vascular\\ndevelopment have been identified (Jin et al, 2007). Using flk1:EGFP transgenic lines which\\nexpresses GFP in all endothelial cells, we categorized these mutations into\\nfour classes: mutations affecting angioblast specification, mutations affecting\\nvascular tube formation, mutations affecting angiogenesis and remodeling\\nprocess, and mutations affecting maintenance of vasculature. Among these, we\\nare interested in first two classes of mutations. Currently, all mutations are\\nmapped on the respective linkage groups. We will pursue positional cloning of\\nthe aforementioned mutants, and analyze their phenotype with molecular,\\ngenetic, and biochemical approaches to understand the functions of the loci\\naffected by these mutations during vascular development.\",\"summary\":\"\\n\\nMy laboratory is interested in understanding how blood vessels form during embryonic development using zebrafish as a model system.
\",\"researchInterests\":[],\"healthInterests\":[],\"researchImagesGallery\":null},\"publications\":[{\"title\":\"Context-dependent proangiogenic function of bone morphogenetic protein signaling is mediated by disabled homolog 2.\",\"citation\":\"Kim JD, Kang H, Larrivée B, Lee MY, Mettlen M, Schmid SL, Roman BL, Qyang Y, Eichmann A, Jin SW. Context-dependent proangiogenic function of bone morphogenetic protein signaling is mediated by disabled homolog 2. Developmental Cell 2012, 23:441-8.\",\"year\":2012,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/22898784\",\"text\":\"Context-dependent proangiogenic function of bone morphogenetic protein signaling is mediated by disabled homolog 2.\"}},{\"title\":\"Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein.\",\"citation\":\"Wiley DM, Kim JD, Hao J, Hong CC, Bautch VL, Jin SW. Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein. Nature Cell Biology 2011, 13:686-92.\",\"year\":2011,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/21572418\",\"text\":\"Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein.\"}},{\"title\":\"Notch signaling functions as a cell-fate switch between the endothelial and hematopoietic lineages.\",\"citation\":\"Lee CY, Vogeli KM, Kim SH, Chong SW, Jiang YJ, Stainier DY, Jin SW. Notch signaling functions as a cell-fate switch between the endothelial and hematopoietic lineages. Current Biology : CB 2009, 19:1616-22.\",\"year\":2009,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/19747827\",\"text\":\"Notch signaling functions as a cell-fate switch between the endothelial and hematopoietic lineages.\"}},{\"title\":\"A transgene-assisted genetic screen identifies essential regulators of vascular development in vertebrate embryos.\",\"citation\":\"Jin SW, Herzog W, Santoro MM, Mitchell TS, Frantsve J, Jungblut B, Beis D, Scott IC, D'Amico LA, Ober EA, Verkade H, Field HA, Chi NC, Wehman AM, Baier H, Stainier DY. A transgene-assisted genetic screen identifies essential regulators of vascular development in vertebrate embryos. Developmental Biology 2007, 307:29-42.\",\"year\":2007,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/17531218\",\"text\":\"A transgene-assisted genetic screen identifies essential regulators of vascular development in vertebrate embryos.\"}},{\"title\":\"A common progenitor for haematopoietic and endothelial lineages in the zebrafish gastrula.\",\"citation\":\"Vogeli KM, Jin SW, Martin GR, Stainier DY. A common progenitor for haematopoietic and endothelial lineages in the zebrafish gastrula. Nature 2006, 443:337-9.\",\"year\":2006,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/16988712\",\"text\":\"A common progenitor for haematopoietic and endothelial lineages in the zebrafish gastrula.\"}},{\"title\":\"Cellular and molecular analyses of vascular tube and lumen formation in zebrafish.\",\"citation\":\"Jin SW, Beis D, Mitchell T, Chen JN, Stainier DY. Cellular and molecular analyses of vascular tube and lumen formation in zebrafish. Development (Cambridge, England) 2005, 132:5199-209.\",\"year\":2005,\"link\":{\"url\":\"https://www.ncbi.nlm.nih.gov/pubmed/16251212\",\"text\":\"Cellular and molecular analyses of vascular tube and lumen formation in zebrafish.\"}}],\"clinicalTrials\":[],\"coauthors\":[]},\"patientCareTab\":null,\"newsTab\":{\"searchUrl\":null,\"news\":[{\"id\":\"5244\",\"bylineDate\":\"2013-04-29T04:00:00-04:00\",\"title\":\"International symposium on lymphatic circulation begins on Friday\",\"summary\":\"Yale School of Medicine and the North American Vascular Biology Organization are pleased to present a special symposium, “Lymphatic Circulation in Health and Disease,” on Friday, May 3, and Saturday, May 4, at the Omni Hotel in New Haven.\",\"thumbnail\":{\"url\":\"https://ysm-res.cloudinary.com/image/upload/v1/yms/prod/9510ecd8-ae10-4c37-b622-10e1d2186d08\",\"altText\":null,\"width\":1500,\"height\":1968,\"imageVariants\":[]},\"url\":\"/intmed/cardio/ycvrc/news-article/5244/\",\"isFeatured\":false,\"source\":null},{\"id\":\"1739\",\"bylineDate\":\"2012-05-01T04:00:00-04:00\",\"title\":\"Cardiovascular science as social network\",\"summary\":\"In bringing cardiovascular researchers together under one roof, Yale center gathers momentum and funding, stimulates scientific collaboration.\",\"thumbnail\":null,\"url\":\"http://medicineatyale.org/may2012/news/newsarticles/124813\",\"isFeatured\":false,\"source\":\"Medicine@Yale\"}]},\"locationsTab\":{\"addresses\":[{\"id\":924,\"address\":{\"id\":348,\"officeName\":null,\"name\":null,\"addressLine1\":\"300 George Street\",\"addressLine2\":\"Ste 770G\",\"city\":\"New Haven\",\"region\":\"CT\",\"country\":\"United 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Notch signaling functions as a cell-fate switch between the endothelial and hematopoietic lineages. 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