Literature DB >> 26494780

Vascular Smooth Muscle Cells From Hypertensive Patient-Derived Induced Pluripotent Stem Cells to Advance Hypertension Pharmacogenomics.

Nikolett M Biel1, Katherine E Santostefano1, Bayli B DiVita1, Nihal El Rouby2, Santiago D Carrasquilla3, Chelsey Simmons4, Mahito Nakanishi5, Rhonda M Cooper-DeHoff6, Julie A Johnson6, Naohiro Terada7.   

Abstract

UNLABELLED: Studies in hypertension (HTN) pharmacogenomics seek to identify genetic sources of variable antihypertensive drug response. Genetic association studies have detected single-nucleotide polymorphisms (SNPs) that link to drug responses; however, to understand mechanisms underlying how genetic traits alter drug responses, a biological interface is needed. Patient-derived induced pluripotent stem cells (iPSCs) provide a potential source for studying otherwise inaccessible tissues that may be important to antihypertensive drug response. The present study established multiple iPSC lines from an HTN pharmacogenomics cohort. We demonstrated that established HTN iPSCs can robustly and reproducibly differentiate into functional vascular smooth muscle cells (VSMCs), a cell type most relevant to vasculature tone control. Moreover, a sensitive traction force microscopy assay demonstrated that iPSC-derived VSMCs show a quantitative contractile response on physiological stimulus of endothelin-1. Furthermore, the inflammatory chemokine tumor necrosis factor α induced a typical VSMC response in iPSC-derived VSMCs. These studies pave the way for a large research initiative to decode biological significance of identified SNPs in hypertension pharmacogenomics. SIGNIFICANCE: Treatment of hypertension remains suboptimal, and a pharmacogenomics approach seeks to identify genetic biomarkers that could be used to guide treatment decisions; however, it is important to understand the biological underpinnings of genetic associations. Mouse models do not accurately recapitulate individual patient responses based on their genetics, and hypertension-relevant cells are difficult to obtain from patients. Induced pluripotent stem cell (iPSC) technology provides a great interface to bring patient cells with their genomic data into the laboratory and to study hypertensive responses. As an initial step, the present study established an iPSC bank from patients with primary hypertension and demonstrated an effective and reproducible method of generating functional vascular smooth muscle cells. ©AlphaMed Press.

Entities:  

Keywords:  Hypertension; Induced pluripotent stem cells; Personalized medicine; Vascular smooth muscle cells

Mesh:

Year:  2015        PMID: 26494780      PMCID: PMC4675511          DOI: 10.5966/sctm.2015-0126

Source DB:  PubMed          Journal:  Stem Cells Transl Med        ISSN: 2157-6564            Impact factor:   6.940


  40 in total

1.  Concurrent generation of functional smooth muscle and endothelial cells via a vascular progenitor.

Authors:  Melanie Marchand; Erica K Anderson; Smruti M Phadnis; Michael T Longaker; John P Cooke; Bertha Chen; Renee A Reijo Pera
Journal:  Stem Cells Transl Med       Date:  2013-12-05       Impact factor: 6.940

Review 2.  The function of myosin and myosin light chain kinase phosphorylation in smooth muscle.

Authors:  K E Kamm; J T Stull
Journal:  Annu Rev Pharmacol Toxicol       Date:  1985       Impact factor: 13.820

Review 3.  Protein kinase C isoforms as specific targets for modulation of vascular smooth muscle function in hypertension.

Authors:  Daisy A Salamanca; Raouf A Khalil
Journal:  Biochem Pharmacol       Date:  2005-09-01       Impact factor: 5.858

4.  Induced pluripotent stem cells as a next-generation biomedical interface.

Authors:  Katherine E Hankowski; Takashi Hamazaki; Akihiro Umezawa; Naohiro Terada
Journal:  Lab Invest       Date:  2011-05-09       Impact factor: 5.662

5.  Functional recapitulation of smooth muscle cells via induced pluripotent stem cells from human aortic smooth muscle cells.

Authors:  Tae-Hee Lee; Sun-Hwa Song; Koung Li Kim; Ji-Yeun Yi; Ga-Hee Shin; Ji Yeon Kim; Jihoon Kim; Yong-Mahn Han; Sang Hun Lee; Suk-Ho Lee; Sung Han Shim; Wonhee Suh
Journal:  Circ Res       Date:  2009-12-03       Impact factor: 17.367

6.  Mechano-coupling and regulation of contractility by the vinculin tail domain.

Authors:  Claudia Tanja Mierke; Philip Kollmannsberger; Daniel Paranhos Zitterbart; James Smith; Ben Fabry; Wolfgang Heinrich Goldmann
Journal:  Biophys J       Date:  2007-09-21       Impact factor: 4.033

7.  Pharmacogenomics of antihypertensive drugs: rationale and design of the Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) study.

Authors:  Julie A Johnson; Eric Boerwinkle; Issam Zineh; Arlene B Chapman; Kent Bailey; Rhonda M Cooper-DeHoff; John Gums; R Whit Curry; Yan Gong; Amber L Beitelshees; Gary Schwartz; Stephen T Turner
Journal:  Am Heart J       Date:  2009-03       Impact factor: 4.749

8.  Vital signs: awareness and treatment of uncontrolled hypertension among adults--United States, 2003-2010.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2012-09-07       Impact factor: 17.586

Review 9.  Novel stem cell-based drug discovery platforms for cardiovascular disease.

Authors:  William J Adams; Guillermo García-Cardeña
Journal:  J Biomol Screen       Date:  2012-08-01

10.  Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy.

Authors:  D Zhi; M R Irvin; C C Gu; A J Stoddard; R Lorier; A Matter; D C Rao; V Srinivasasainagendra; H K Tiwari; A Turner; U Broeckel; D K Arnett
Journal:  Front Genet       Date:  2012-05-28       Impact factor: 4.599

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  21 in total

Review 1.  Concise Review: Induced Pluripotent Stem Cell Research in the Era of Precision Medicine.

Authors:  Takashi Hamazaki; Nihal El Rouby; Natalie C Fredette; Katherine E Santostefano; Naohiro Terada
Journal:  Stem Cells       Date:  2017-02-05       Impact factor: 6.277

Review 2.  Induced Pluripotent Stem Cell-Derived Endothelial Cells: Overview, Current Advances, Applications, and Future Directions.

Authors:  Sae Jang; Alexandra Collin de l'Hortet; Alejandro Soto-Gutierrez
Journal:  Am J Pathol       Date:  2019-01-14       Impact factor: 4.307

Review 3.  Human In Vitro Models for Assessing the Genomic Basis of Chemotherapy-Induced Cardiovascular Toxicity.

Authors:  Emily A Pinheiro; Tarek Magdy; Paul W Burridge
Journal:  J Cardiovasc Transl Res       Date:  2020-02-20       Impact factor: 4.132

Review 4.  Stem cell manipulation, gene therapy and the risk of cancer stem cell emergence.

Authors:  Flora Clément; Elodie Grockowiak; Florence Zylbersztejn; Gaëlle Fossard; Stéphanie Gobert; Véronique Maguer-Satta
Journal:  Stem Cell Investig       Date:  2017-07-25

5.  Efficient differentiation of vascular smooth muscle cells from Wharton's Jelly mesenchymal stromal cells using human platelet lysate: A potential cell source for small blood vessel engineering.

Authors:  Panagiotis Mallis; Aggeliki Papapanagiotou; Michalis Katsimpoulas; Alkiviadis Kostakis; Gerasimos Siasos; Eva Kassi; Catherine Stavropoulos-Giokas; Efstathios Michalopoulos
Journal:  World J Stem Cells       Date:  2020-03-26       Impact factor: 5.326

Review 6.  hiPSCs in cardio-oncology: deciphering the genomics.

Authors:  Emily A Pinheiro; K Ashley Fetterman; Paul W Burridge
Journal:  Cardiovasc Res       Date:  2019-04-15       Impact factor: 10.787

7.  A hypertension patient-derived iPSC model demonstrates a role for G protein-coupled estrogen receptor in hypertension risk and development.

Authors:  Natalie C Fredette; Eliyah Malik; Marah L Mukhtar; Eric R Prossnitz; Naohiro Terada
Journal:  Am J Physiol Cell Physiol       Date:  2020-08-12       Impact factor: 4.249

Review 8.  Redox Stress Defines the Small Artery Vasculopathy of Hypertension: How Do We Bridge the Bench-to-Bedside Gap?

Authors:  Rhian M Touyz; Augusto C Montezano; Francisco Rios; Michael E Widlansky; Mingyu Liang
Journal:  Circ Res       Date:  2017-05-26       Impact factor: 17.367

9.  Generation of Induced Pluripotent Stem Cells from a Female Patient with a Xq27.3-q28 Deletion to Establish Disease Models and Identify Therapies.

Authors:  Noriko Watanabe; Kohei Kitada; Katherine E Santostefano; Airi Yokoyama; Sara M Waldrop; Coy D Heldermon; Daisuke Tachibana; Masayasu Koyama; Amy M Meacham; Christina A Pacak; Naohiro Terada
Journal:  Cell Reprogram       Date:  2020-06-30       Impact factor: 1.987

Review 10.  Quantifying cellular forces: Practical considerations of traction force microscopy for dermal fibroblasts.

Authors:  Abigail De La Pena; Marah Mukhtar; Ryosuke Yokosawa; Santiago Carrasquilla; Chelsey S Simmons
Journal:  Exp Dermatol       Date:  2020-09-21       Impact factor: 3.960

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