Modeling of skeletal development and diseases using human pluripotent stem cells

被引:0
作者
Hojo, Hironori [1 ,2 ]
Tani, Shoichiro [3 ]
Ohba, Shinsuke [4 ]
机构
[1] Univ Tokyo, Ctr Dis Biol & Integrat Med, Grad Sch Med, Div Clin Biotechnol, Tokyo 1138655, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Bioengn, Tokyo 1138655, Japan
[3] Univ Texas Southwestern Med Ctr, Childrens Med Ctr Res Inst, Dallas, TX 75390 USA
[4] Osaka Univ, Grad Sch Dent, Dept Tissue & Dev Biol, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
human pluripotent stem cells; skeletal development; disease modeling; osteoblasts; chondrocytes; ON-A-CHIP; HUMAN SEGMENTATION CLOCK; NEURAL CREST CELLS; OSTEOBLAST DIFFERENTIATION; BONE REGENERATION; SHH ESTABLISHES; AXIAL SKELETON; FEEDBACK LOOP; MESODERM; BMP;
D O I
10.1093/jbmr/zjae178
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human skeletal elements are formed from distinct origins at distinct positions of the embryo. For example, the neural crest produces the facial bones, the paraxial mesoderm produces the axial skeleton, and the lateral plate mesoderm produces the appendicular skeleton. During skeletal development, different combinations of signaling pathways are coordinated from distinct origins during the sequential developmental stages. Models for human skeletal development have been established using human pluripotent stem cells (hPSCs) and by exploiting our understanding of skeletal development. Stepwise protocols for generating skeletal cells from different origins have been designed to mimic developmental trails. Recently, organoid methods have allowed the multicellular organization of skeletal cell types to recapitulate complicated skeletal development and metabolism. Similarly, several genetic diseases of the skeleton have been modeled using patient-derived induced pluripotent stem cells and genome-editing technologies. Model-based drug screening is a powerful tool for identifying drug candidates. This review briefly summarizes our current understanding of the embryonic development of skeletal tissues and introduces the current state-of-the-art hPSC methods for recapitulating skeletal development, metabolism, and diseases. We also discuss the current limitations and future perspectives for applications of the hPSC-based modeling system in precision medicine in this research field. Human bones have different origins in the embryo: facial bones originate from the neural crest, axial skeleton from the paraxial mesoderm, and limb bones from the lateral plate mesoderm. Human stem cells have been used to model bone development by mimicking the developmental processes. Recent advancements, such as organoid methods, have helped recreate complex bone development. Genetic bone diseases have also been studied using stem cells and gene editing technology. These models hold promise for improving precision medicine. This review overviews our understanding of bone development, introduces current advancements, and provides future perspectives for bone and stem cell research.
引用
收藏
页码:5 / 19
页数:15
相关论文
共 136 条
  • [1] Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors
    Akiyama, H
    Kim, JE
    Nakashima, K
    Balmes, G
    Iwai, N
    Deng, JM
    Zhang, ZP
    Martin, JF
    Behringer, RR
    Nakamura, T
    de Crombrugghe, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) : 14665 - 14670
  • [2] Signaling Gradients during Paraxial Mesoderm Development
    Aulehla, Alexander
    Pourquie, Olivier
    [J]. COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (02): : a000869
  • [3] Single-Cell RNA Sequencing of Calvarial and Long-Bone Endocortical Cells
    Ayturk, Ugur M.
    Scollan, Joseph P.
    Goz Ayturk, Didem
    Suh, Eun Sung
    Vesprey, Alexander
    Jacobsen, Christina M.
    Divieti Pajevic, Paola
    Warman, Matthew L.
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2020, 35 (10) : 1981 - 1991
  • [4] CHD7 cooperates with PBAF to control multipotent neural crest formation
    Bajpai, Ruchi
    Chen, Denise A.
    Rada-Iglesias, Alvaro
    Zhang, Junmei
    Xiong, Yiqin
    Helms, Jill
    Chang, Ching-Pin
    Zhao, Yingming
    Swigut, Tomek
    Wysocka, Joanna
    [J]. NATURE, 2010, 463 (7283) : 958 - U135
  • [5] Balmer S, 2016, DEV DYNAM, V245, P547, DOI [10.1002/DVDY.24392, 10.1002/dvdy.24392]
  • [6] 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
  • [7] The nodal precursor acting via activin receptors induces mesoderm by maintaining a source of its convertases and BMP4
    Ben-Haim, Nadav
    Lu, Cindy
    Guzman-Ayala, Marcela
    Pescatore, Luca
    Mesnard, Daniel
    Bischofberger, Mirko
    Naef, Felix
    Robertson, Elizabeth J.
    Constam, Daniel B.
    [J]. DEVELOPMENTAL CELL, 2006, 11 (03) : 313 - 323
  • [8] Lineage analysis of the avian dermomyotome sheet reveals the existence of single cells with both dermal and muscle progenitor fates
    Ben-Yair, R
    Kalcheim, C
    [J]. DEVELOPMENT, 2005, 132 (04): : 689 - 701
  • [9] AN ANCIENT FAMILY OF EMBRYONICALLY EXPRESSED MOUSE GENES SHARING A CONSERVED PROTEIN MOTIF WITH THE T-LOCUS
    BOLLAG, RJ
    SIEGFRIED, Z
    CEBRATHOMAS, JA
    GARVEY, N
    DAVIDSON, EM
    SILVER, LM
    [J]. NATURE GENETICS, 1994, 7 (03) : 383 - 389
  • [10] Brault V, 2001, DEVELOPMENT, V128, P1253