RNA-Binding Proteins: Emerging Therapeutics for Vascular Dysfunction

被引:14
作者
Cornelius, Victoria A. [1 ]
Naderi-Meshkin, Hojjat [1 ]
Kelaini, Sophia [1 ]
Margariti, Andriana [1 ]
机构
[1] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Wellcome Wolfson Inst Expt Med, 97 Lisburn Rd, Belfast BT9 7BL, Antrim, North Ireland
关键词
vascular disease; RNA-binding proteins; stem cell technologies; iPSCs; Quaking; QKI; TRANSCRIPTOME-WIDE DISCOVERY; PLURIPOTENT STEM-CELLS; SMOOTH-MUSCLE-CELLS; MESSENGER-RNA; ENDOTHELIAL-CELLS; GENE-EXPRESSION; DEFICIENT MICE; QUAKING; HUR; TARGET;
D O I
10.3390/cells11162494
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Vascular diseases account for a significant number of deaths worldwide, with cardiovascular diseases remaining the leading cause of mortality. This ongoing, ever-increasing burden has made the need for an effective treatment strategy a global priority. Recent advances in regenerative medicine, largely the derivation and use of induced pluripotent stem cell (iPSC) technologies as disease models, have provided powerful tools to study the different cell types that comprise the vascular system, allowing for a greater understanding of the molecular mechanisms behind vascular health. iPSC disease models consequently offer an exciting strategy to deepen our understanding of disease as well as develop new therapeutic avenues with clinical translation. Both transcriptional and post-transcriptional mechanisms are widely accepted to have fundamental roles in orchestrating responses to vascular damage. Recently, iPSC technologies have increased our understanding of RNA-binding proteins (RBPs) in controlling gene expression and cellular functions, providing an insight into the onset and progression of vascular dysfunction. Revelations of such roles within vascular disease states have therefore allowed for a greater clarification of disease mechanisms, aiding the development of novel therapeutic interventions. Here, we discuss newly discovered roles of RBPs within the cardio-vasculature aided by iPSC technologies, as well as examine their therapeutic potential, with a particular focus on the Quaking family of isoforms.
引用
收藏
页数:16
相关论文
共 108 条
  • [1] The PKCβ/HuR/VEGF pathway in diabetic retinopathy
    Amadio, M.
    Bucolo, C.
    Leggio, G. M.
    Drago, F.
    Govoni, S.
    Pascale, A.
    [J]. BIOCHEMICAL PHARMACOLOGY, 2010, 80 (08) : 1230 - 1237
  • [2] PKCβII/HuR/VEGF:: A new molecular cascade in retinal pericytes for the regulation of VEGF gene expression
    Amadio, Marialaura
    Scapagnini, Giovanni
    Lupo, Gabriella
    Drago, Filippo
    Govoni, Stefano
    Pascale, Alessia
    [J]. PHARMACOLOGICAL RESEARCH, 2008, 57 (01) : 60 - 66
  • [3] Nanosystems based on siRNA silencing HuR expression counteract diabetic retinopathy in rat
    Amadio, Marialaura
    Pascale, Alessia
    Cupri, Sarha
    Pignatello, Rosario
    Osera, Cecilia
    D'Agata, Velia
    D'Amico, Agata Grazia
    Leggio, Gian Marco
    Ruozi, Barbara
    Govoni, Stefano
    Dragon, Filippo
    Bucolo, Claudio
    [J]. PHARMACOLOGICAL RESEARCH, 2016, 111 : 713 - 720
  • [4] RNA-Based Therapeutics: From Antisense Oligonucleotides to miRNAs
    Bajan, Sarah
    Hutvagner, Gyorgy
    [J]. CELLS, 2020, 9 (01)
  • [5] The RNA-binding proteomes from yeast to man harbour conserved enigmRBPs
    Beckmann, Benedikt M.
    Horos, Rastislav
    Fischer, Bernd
    Castello, Alfredo
    Eichelbaum, Katrin
    Alleaume, Anne-Marie
    Schwarzl, Thomas
    Curk, Tomaz
    Foehr, Sophia
    Huber, Wolfgang
    Krijgsveld, Jeroen
    Hentze, Matthias W.
    [J]. NATURE COMMUNICATIONS, 2015, 6
  • [6] Human Vascular Tissue Models Formed from Human Induced Pluripotent Stem Cell Derived Endothelial Cells
    Belair, David G.
    Whisler, Jordan A.
    Valdez, Jorge
    Velazquez, Jeremy
    Molenda, James A.
    Vickerman, Vernella
    Lewis, Rachel
    Daigh, Christine
    Hansen, Tyler D.
    Mann, David A.
    Thomson, James A.
    Griffith, Linda G.
    Kamm, Roger D.
    Schwartz, Michael P.
    Murphy, William L.
    [J]. STEM CELL REVIEWS AND REPORTS, 2015, 11 (03) : 511 - 525
  • [7] The epidemiology of cardiovascular disease in the UK 2014
    Bhatnagar, Prachi
    Wickramasinghe, Kremlin
    Williams, Julianne
    Rayner, Mike
    Townsend, Nick
    [J]. HEART, 2015, 101 (15) : 1182 - 1189
  • [8] Endothelial Dysfunction in Tristetraprolin-deficient Mice Is Not Caused by Enhanced Tumor Necrosis Factor-α Expression
    Bollmann, Franziska
    Wu, Zhixiong
    Oelze, Matthias
    Siuda, Daniel
    Xia, Ning
    Henke, Jenny
    Daiber, Andreas
    Li, Huige
    Stumpo, Deborah J.
    Blackshear, Perry J.
    Kleinert, Hartmut
    Pautz, Andrea
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (22) : 15653 - 15665
  • [9] oRNAment: a database of putative RNA binding protein target sites in the transcriptomes of model species
    Bouvrette, Louis Philip Benoit
    Bovaird, Samantha
    Blanchette, Mathieu
    Lecuyer, Eric
    [J]. NUCLEIC ACIDS RESEARCH, 2020, 48 (D1) : D166 - D173
  • [10] RNA editing
    Brennicke, A
    Marchfelder, A
    Binder, S
    [J]. FEMS MICROBIOLOGY REVIEWS, 1999, 23 (03) : 297 - 316