Developmental principles informing human pluripotent stem cell differentiation to cartilage and bone

被引:12
作者
Humphreys, Paul A. [1 ,2 ,3 ]
Mancini, Fabrizio E. [1 ]
Ferreira, Miguel J. S. [1 ,2 ,3 ]
Woods, Steven [1 ]
Ogene, Leona [1 ]
Kimber, Susan J. [1 ]
机构
[1] Univ Manchester, Fac Biol, Sch Biol Sci, Div Cell Matrix Biol & Regenerat Med, Manchester, England
[2] Univ Manchester, Fac Sci & Engn, Sch Engn, Dept Mech Aerosp & Civil Engn, Manchester, England
[3] Univ Manchester, Henry Royce Inst, Manchester, England
基金
英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
Pluripotent stem cells; human development; cartilage; bone; chondrogenesis; growth-plate; modeling; mesoderm; neural-crest; osteogenesis; skeletonenesis; skeleton; NEURAL CREST CELLS; MESENCHYMAL STROMAL CELLS; TRANSCRIPTION FACTOR ERG; TGF-BETA; ARTICULAR-CARTILAGE; INDIAN HEDGEHOG; PROGENITOR CELLS; SYNOVIAL JOINT; MOUSE LIMB; CHONDROCYTE PROLIFERATION;
D O I
10.1016/j.semcdb.2021.11.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human pluripotent stem cells can differentiate into any cell type given appropriate signals and hence have been used to research early human development of many tissues and diseases. Here, we review the major biological factors that regulate cartilage and bone development through the three main routes of neural crest, lateral plate mesoderm and paraxial mesoderm. We examine how these routes have been used in differentiation protocols that replicate skeletal development using human pluripotent stem cells and how these methods have been refined and improved over time. Finally, we discuss how pluripotent stem cells can be employed to understand human skeletal genetic diseases with a developmental origin and phenotype, and how developmental protocols have been applied to gain a better understanding of these conditions.
引用
收藏
页码:17 / 36
页数:20
相关论文
共 259 条
  • [1] Neural crest stem cells: discovery, properties and potential for therapy
    Achilleos, Annita
    Trainor, Paul A.
    [J]. CELL RESEARCH, 2012, 22 (02) : 288 - 304
  • [2] Step-Wise Chondrogenesis of Human Induced Pluripotent Stem Cells and Purification Via a Reporter Allele Generated by CRISPR-Cas9 Genome Editing
    Adkar, Shaunak S.
    Wu, Chia-Lung
    Willard, Vincent P.
    Dicks, Amanda
    Ettyreddy, Adarsh
    Steward, Nancy
    Bhutani, Nidhi
    Gersbach, Charles A.
    Guilak, Farshid
    [J]. STEM CELLS, 2019, 37 (01) : 65 - 76
  • [3] Dynamic mechanical loading and growth factors influence chondrogenesis of induced pluripotent mesenchymal progenitor cells in a cartilage-mimetic hydrogel
    Aisenbrey, Elizabeth A.
    Bilousova, Ganna
    Payne, Karin
    Bryant, Stephanie J.
    [J]. BIOMATERIALS SCIENCE, 2019, 7 (12) : 5388 - 5403
  • [4] Isogenic Pairs of Wild Type and Mutant Induced Pluripotent Stem Cell (iPSC) Lines from Rett Syndrome Patients as In Vitro Disease Model
    Ananiev, Gene
    Williams, Emily Cunningham
    Li, Hongda
    Chang, Qiang
    [J]. PLOS ONE, 2011, 6 (09):
  • [5] Efficient and Rapid Induction of Human iPSCs/ESCs into Nephrogenic Intermediate Mesoderm Using Small Molecule-Based Differentiation Methods
    Araoka, Toshikazu
    Mae, Shin-ichi
    Kurose, Yuko
    Uesugi, Motonari
    Ohta, Akira
    Yamanaka, Shinya
    Osafune, Kenji
    [J]. PLOS ONE, 2014, 9 (01):
  • [6] Signaling Gradients during Paraxial Mesoderm Development
    Aulehla, Alexander
    Pourquie, Olivier
    [J]. COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (02): : a000869
  • [7] Mouse gastrulation: Coordination of tissue patterning, specification and diversification of cell fate
    Bardot, Evan S.
    Hadjantonakis, Anna-Katerina
    [J]. MECHANISMS OF DEVELOPMENT, 2020, 163
  • [8] Visualization of cartilage formation: Insight into cellular properties of skeletal progenitors and chondrodysplasia syndromes
    Barna, Maria
    Niswander, Lee
    [J]. DEVELOPMENTAL CELL, 2007, 12 (06) : 931 - 941
  • [9] CLONE-FORMING ABILITY AND DIFFERENTIATION POTENTIAL OF MIGRATORY NEURAL CREST CELLS
    BAROFFIO, A
    DUPIN, E
    LEDOUARIN, NM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (14) : 5325 - 5329
  • [10] A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep
    Beever, JE
    Smit, MA
    Meyers, SN
    Hadfield, TS
    Bottema, C
    Albretsen, J
    Cockett, NE
    [J]. ANIMAL GENETICS, 2006, 37 (01) : 66 - 71