• WELCOME

    ORGANIZER:

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    Dr Camilla Cerutti

    University of Bristol

    EMAIL: camilla.cerutti@bristol.ac.uk

    WEB: http://drcamillacerutti.strikingly.com/

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    SCOPE

    The purpose of the one day Bristol ENDOTHELIAL meeting is to bridge

    all the researchers within the University of Bristol working

    on vasculature and endothelial cells, from basic to clinical research, to foster cross-disciplinary exchange of ideas and expertise to create a Vascular Endothelium Network @UoB

     

    The focus of the meeting is to promote collaborations and

    networking on the vasculature/endothelium themes across

    Faculties and Schools @UoB to increase research impact.

     

    The meeting will give the opportunity to showcase the vascular/endothelium research @UoB

    across disciplines presenting techniques/sample availability/cell types and tools on top of science.

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    FORMAT

    The meeting format will have 5, 10, 15 minutes TALKS and a POSTER session.

     

    I am eager to have as many early career researcher as possible

    to attend and present their research and techniques.

     

    I encourage group leaders, professors and endothelial cell passionate to participate to the meeting and promote the Bristol ENDOTHELIAL meeting within their group/colleagues.

     

    I hope you will enjoy this great day of science!

  • Connect

    Tweet about the Bristol ENDOTHELIAL meeting (BEM2019) @BEM20191

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  • Social Feed

    Check out BEM2019 updates!

  • TIME & PLACE

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    WHEN: 19 SEPTEMBER 2019

     

    TIME: 8:30-5:30

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    WHERE: The FOUNDATION-space event

    St George’s Road at the corner with Deanery Road (see the MAP below)
    Bristol,

    BS1 5AF

     

    (150m from College green bus stop- 100m from the Cathedral)

     

    PUBLIC TRANSPORT: More information can be found at https://travelwest.info/

    CAR: list of public car parks can be found at https://travelwest.info/drive/parking/bristol-car-parking-map

    The closest car park is the College Street pay and display.

    There is also on-street metered parking on Deanery Road.

  • MAP: The FOUNDATION St George’s Road. Bristol, BS1 5BE

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  • PROGRAM

    Download the PROGRAM

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  • GUEST SPEAKERS

    Dr Anjali Kusumbe `Organotypic angiocrine signals in health and disease`

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    University of Oxford

    Medical science divisions Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences Kennedy Institute of Rheumatology

    Anjali Kusumbe was trained in India. She joined the lab of Ralf Adams at the Max Planck Institute for Molecular Biomedicine in Munster as a postdoc fellow. She is currently principal investigator of the group “Tissue and tumor microenvironments” at the Kennedy Institute in Oxford, UK.

    Her group is interested in exploring the contributions of the vasculature in defining the tissue microenvironments and unravelling the changes occurring in the vascular microenvironments during tumour growth. They seek to elucidate the angiocrine signals underlying the regional specialization of tissue microenvironments, and how these specialized vascular niches instruct cell fate and behavior in normal and tumour tissue.

     

    KEY PUBLICATIONS:

    Endothelial proteolytic activity and interaction with non-resorbing osteoclasts mediate bone elongation.

    Romeo SG, Alawi KM, Rodrigues J, Singh A, Kusumbe AP, Ramasamy SK.

    Nat Cell Biol. 2019

    Age-dependent modulation of vascular niches for haematopoietic stem cells.

    Kusumbe AP, Ramasamy SK, Itkin T, Mäe MA, Langen UH, Betsholtz C, Lapidot T, Adams RH.

    Nature. 2016

    Sample preparation for high-resolution 3D confocal imaging of mouse skeletal tissue.

    Kusumbe AP, Ramasamy SK, Starsichova A, Adams RH.

    Nat Protoc. 2015

    Osteoclast progenitors promote bone vascularization and osteogenesis.

    Kusumbe AP, Adams RH.

    Nat Med. 2014

    Coupling of angiogenesis and osteogenesis by a specific vessel subtype in bone.

    Kusumbe AP, Ramasamy SK, Adams RH.

    Nature. 2014

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    Dr Alessandra Granata ' Modelling Small Vessel Disease and stroke using human induced Pluripotent Stem Cells

     

    University of Cambridge

    Cambridge Cardiovascular​

    I lead the research group for modelling cerebrovascular diseases using patient-derived induced pluripotent stem cells (iPSC). I am based at the Clifford Allbutt Building, Central Biomedical Campus, Addenbrooke’s Site and am part of the Stroke Research Group of Professor Hugh Markus, in the department of Clinical Neurosciences.

    My main research interest is to develop iPSC-based model system for genetic forms of cerebral small vessel diseases (SVD), exploiting findings from genome wide association studies (GWAS) and whole genome sequencing studies in ischaemic stroke. We believe that iPSC-derived models can be used to uncover disease mechanisms and to identify new treatments for SVD.

     

    KEY PUBLICATIONS:

    An iPSC-derived vascular model of Marfan syndrome identifies key mediators of smooth muscle cell death.

    Granata A, Serrano F, Bernard WG, McNamara M, Low L, Sastry P, Sinha S. Nat Genet. 2017 Jan;49(1):97-109.

    Temporal and embryonic lineage-dependent regulation of human vascular SMC development by NOTCH3.

    Granata A, Bernard WG, Zhao N, Mccafferty J, Lilly B, Sinha S. Stem Cells Dev. 2015 Apr 1;24(7):846-56.

    Embryonic origins of human vascular smooth muscle cells: implications for in vitro modeling and clinical application. 

    Sinha S, Iyer D, Granata A. Cell Mol Life Sci. 2014 Jun;71(12):2271-88.

     

  • SPEAKERS

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    Miss Rosaria Bianco

    Effect of flow and angiotensin II on endothelial cells with relevance to aneurysm formation

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    Dr Andrew Bond

    Blood outgrowth endothelial cells for tissue engineered vascular grafts

    Arterial bioengineering

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    Eng Michele Carrabba

    Development of Multi-layered Tissue Engineering Vascular Graft for small-diameter vascular replacement

    Tissue Engineering Vascular Graft

    human cell-seeded scaffolds

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    Dr Natalie Finch

    Glomerular endothelial fenestrations

    vascular endothelial

    renal physiology

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    Dr Becky Foster

    Bristol Renal: Models and techniques

    vascular endothelial growth factor (VEGF)-A

    podocyte biology

    renal physiology

    academic renal unit

    proteins involved in glomerular physiology & pathology

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    Prof Sarah George

    Acute endothelial cell inflammation and coronary artery vein graft disease.

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    Wnt

    inflammation

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    Dr Jason L Johnson

    Regulatory role of IL-3 in angiogenesis and neovascularisation

    vascular microRNAs

    MMP

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    Miss Kirsty Lewis

    Platelet-derived extracellular vesicles and platelet secretion in the regulation of endothelial function’

    platelets

    secretion

    microvesicles

    angiogenesis

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    Dr Scott Miners

    Does breakdown in endothelial-pericyte communication underlie vascular dysfunction in Alzheimer's disease?

    Pericytes

    Alzheimer's disease

    beta amyloid

    hypoxia

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    Prof Harry Mellor

    Endothelial cell secretion

    Endothelial cell shape and movement

    Endothelial cell receptor signalling and trafficking

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    Dr Elisa Pedone

    Microfluidic-microscopy platform for ‘on-demand’ dynamic gene expression regulation and signaling pathway activity

    Synthetic Biology

    control theory

    stem cell identity

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    Dr Raina Ramnath and Dr Yan Qiu

    Diabetes and endothelial glycocalyx

    vascular endothelial glycocalyx

    diabetes

    renal physiology

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    Miss Lien Reolizo

    Anti-inflammatory effects of Hhex in endothelial cells

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    inflammation

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    Dr Christopher Rice

    Neutrophil extracellular traps (NETs) promote adhesion of infected red blood cell to vascular endothelium in malaria

    Malaria,

    Neutrophils

    NETs

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    Dr Beck Richardson

    Endothelial cells in cardiac repair and regeneration in adult zebrafish

    wound healing

    human disease

    cardiovascular disease

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    Dr Tony Walsh

    Platelet-derived extracellular vesicles and platelet secretion in the regulation of endothelial function’

    platelets

    secretion

    microvesicles

    angiogenesis

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    Dr Helen Weavers

    Modelling immune cell extravasation from vessels to wounds using in vivo Drosophila and mouse models

    immune cell extravasation

    wound inflammation

    Drosophila model

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    Mr Aaron Scott​

    In vivo characterisation of endothelial-derived extracellular vesicles in zebrafish

    extracellular vescicles

  • SPEAKERS- FACILITY

    vascular and endothelial research

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    IMAGING FACILITY

    Dr Mark Jepson Imaging Facility Manager

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    FLOW CYTOMETRY FACILITY

    Dr Andrew Herman Flow Facility Manager

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    PROTEOMIC FACILITY

    Dr Kate Heesom Proteomics Facility Manager

  • POSTER session 

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    PREPARE you poster

    There are not SIZE or ORIENTATION restrictions

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    Poster POSITION at BEM2019

    • the poster AREA is located at the far end of the event space (entering turn left)
    • please find a TAG with your name and number on the walls
    • white blue tack to hang them will be provided (by the tag)
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    Poster ASSESSMENT

    The poster assessment will be is divided in 2 sub-session over lunch:

     

    GROUP A – POSTER 1 to 6

    13:15-13:45

     

    GROUP B – POSTER 7 to 12

    13:45-14:15

     

    Please be at your poster to present it for all 30 minutes.

  • Registration

    Regular Admission is FREE

    It includes the event with coffee breaks and lunch.

     

    FREE coffee, tea and water will be available all day.

     

    All the speakers and poster presenters HAVE to register.

    See you there!

    REGISTRATION DEADLINE: 10 SEPTEMBER 2019