Timing and Graded BMP Signalling Determines Fate of Neural Crest and Ectodermal Placode Derivatives from Pluripotent Stem Cells

被引:0
|
作者
Chung, Keshi [1 ]
Millet, Malvina [1 ,2 ]
Rouillon, Ludivine [1 ]
Zine, Azel [1 ]
机构
[1] Univ Montpellier, Lab Bioengn & Nanosci, LBN, F-34193 Montpellier, France
[2] Harvard Med Sch, Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
关键词
bone morphogenetic proteins; human pluripotent stem cells; human cell models; organoids; pre-placodal ectoderm; otic lineage; BONE MORPHOGENETIC PROTEINS; PREAXIAL BRACHYDACTYLY SYNDROME; CARDIAC DIFFERENTIATION; PROXIMAL SYMPHALANGISM; RETINOIC ACID; MESSENGER-RNA; SELF-RENEWAL; ACTIVIN-A; L-MAF; MUTATION;
D O I
10.3390/biomedicines12102262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pluripotent stem cells (PSCs) offer many potential research and clinical benefits due to their ability to differentiate into nearly every cell type in the body. They are often used as model systems to study early stages of ontogenesis to better understand key developmental pathways, as well as for drug screening. However, in order to fully realise the potential of PSCs and their translational applications, a deeper understanding of developmental pathways, especially in humans, is required. Several signalling molecules play important roles during development and are required for proper differentiation of PSCs. The concentration and timing of signal activation are important, with perturbations resulting in improper development and/or pathology. Bone morphogenetic proteins (BMPs) are one such key group of signalling molecules involved in the specification and differentiation of various cell types and tissues in the human body, including those related to tooth and otic development. In this review, we describe the role of BMP signalling and its regulation, the consequences of BMP dysregulation in disease and differentiation, and how PSCs can be used to investigate the effects of BMP modulation during development, mainly focusing on otic development. Finally, we emphasise the unique role of BMP4 in otic specification and how refined understanding of controlling its regulation could lead to the generation of more robust and reproducible human PSC-derived otic organoids for research and translational applications.
引用
收藏
页数:22
相关论文
共 50 条
  • [1] Specification of Functional Cranial Placode Derivatives from Human Pluripotent Stem Cells
    Dincer, Zehra
    Piao, Jinghua
    Niu, Lei
    Ganat, Yosif
    Kriks, Sonja
    Zimmer, Bastian
    Shi, Song-Hai
    Tabar, Viviane
    Studer, Lorenz
    CELL REPORTS, 2013, 5 (05): : 1387 - 1402
  • [2] Derivation of neural crest cells from human pluripotent stem cells
    Lee, Gabsang
    Chambers, Stuart M.
    Tomishima, Mark J.
    Studer, Lorenz
    NATURE PROTOCOLS, 2010, 5 (04) : 688 - 701
  • [3] Derivation of neural crest cells from human pluripotent stem cells
    Gabsang Lee
    Stuart M Chambers
    Mark J Tomishima
    Lorenz Studer
    Nature Protocols, 2010, 5 : 688 - 701
  • [4] Efficient induction of neural crest cells from human pluripotent stem cells
    Tanaka, Hiroshi
    Nakai, Yoshinori
    Fukuta, Makoto
    Ueno, Morio
    Ikeya, Makoto
    Toguchida, Junya
    Kinoshita, Shigeru
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [5] Generating trunk neural crest from human pluripotent stem cells
    Huang, Miller
    Miller, Matthew L.
    McHenry, Lauren K.
    Zheng, Tina
    Zhen, Qiqi
    Ilkhanizadeh, Shirin
    Conklin, Bruce R.
    Bronner, Marianne E.
    Weiss, William A.
    SCIENTIFIC REPORTS, 2016, 6
  • [6] Generating trunk neural crest from human pluripotent stem cells
    Miller Huang
    Matthew L. Miller
    Lauren K. McHenry
    Tina Zheng
    Qiqi Zhen
    Shirin Ilkhanizadeh
    Bruce R. Conklin
    Marianne E. Bronner
    William A. Weiss
    Scientific Reports, 6
  • [7] Generation of Induced Pluripotent Stem Cells from Hair Follicle Bulge Neural Crest Stem Cells
    Ma, Ming-San
    Czepiel, Marcin
    Krause, Tina
    Schaefer, Karl-Herbert
    Boddeke, Erik
    Copray, Sjef
    CELLULAR REPROGRAMMING, 2014, 16 (05) : 307 - 313
  • [8] Protein Kinase C Modulation Determines the Mesoderm/Extraembryonic Fate Under BMP4 Induction From Human Pluripotent Stem Cells
    Godoy-Parejo, Carlos
    Deng, Chunhao
    Xu, Jiaqi
    Zhang, Zhaoying
    Ren, Zhili
    Ai, Nana
    Liu, Weiwei
    Ge, Wei
    Deng, Chuxia
    Xu, Xiaoling
    Chin, Y. Eugene
    Chen, Guokai
    STEM CELLS, 2023, 41 (06) : 578 - 591
  • [9] Immunological Properties of Neural Crest Cells Derived from Human Induced Pluripotent Stem Cells
    Fujii, Shota
    Yoshida, Satoru
    Inagaki, Emi
    Hatou, Shin
    Tsubota, Kazuo
    Takahashi, Masayo
    Shimmura, Shigeto
    Sugita, Sunao
    STEM CELLS AND DEVELOPMENT, 2019, 28 (01) : 28 - 43
  • [10] Characterization and transplantation of enteric neural crest cells from human induced pluripotent stem cells
    W Li
    L Huang
    J Zeng
    W Lin
    K Li
    J Sun
    W Huang
    J Chen
    G Wang
    Q Ke
    J Duan
    X Lai
    R Chen
    M Liu
    Y Liu
    T Wang
    X Yang
    Y Chen
    H Xia
    A P Xiang
    Molecular Psychiatry, 2018, 23 : 499 - 508