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Plexin-B2 orchestrates collective stem cell dynamics via actomyosin contractility, cytoskeletal tension and adhesion

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  • Chrystian Junqueira Alves

    (Icahn School of Medicine at Mount Sinai)

  • Rafael Dariolli

    (Icahn School of Medicine at Mount Sinai)

  • Jonathan Haydak

    (Icahn School of Medicine at Mount Sinai)

  • Sangjo Kang

    (Icahn School of Medicine at Mount Sinai)

  • Theodore Hannah

    (Icahn School of Medicine at Mount Sinai)

  • Robert J. Wiener

    (Icahn School of Medicine at Mount Sinai)

  • Stefanie DeFronzo

    (Icahn School of Medicine at Mount Sinai)

  • Rut Tejero

    (Icahn School of Medicine at Mount Sinai)

  • Gabriele L. Gusella

    (Icahn School of Medicine at Mount Sinai)

  • Aarthi Ramakrishnan

    (Icahn School of Medicine at Mount Sinai)

  • Rodrigo Alves Dias

    (Federal University of Juiz de Fora)

  • Alexandre Wojcinski

    (Pacific Neuroscience Institute and John Wayne Cancer Institute at Providence Saint John’s Health Center)

  • Santosh Kesari

    (Pacific Neuroscience Institute and John Wayne Cancer Institute at Providence Saint John’s Health Center)

  • Li Shen

    (Icahn School of Medicine at Mount Sinai)

  • Eric A. Sobie

    (Icahn School of Medicine at Mount Sinai)

  • José Paulo Rodrigues Furtado de Mendonça

    (Federal University of Juiz de Fora)

  • Evren U. Azeloglu

    (Icahn School of Medicine at Mount Sinai
    Icahn School of Medicine at Mount Sinai)

  • Hongyan Zou

    (Icahn School of Medicine at Mount Sinai
    Icahn School of Medicine at Mount Sinai)

  • Roland H. Friedel

    (Icahn School of Medicine at Mount Sinai
    Icahn School of Medicine at Mount Sinai)

Abstract

During morphogenesis, molecular mechanisms that orchestrate biomechanical dynamics across cells remain unclear. Here, we show a role of guidance receptor Plexin-B2 in organizing actomyosin network and adhesion complexes during multicellular development of human embryonic stem cells and neuroprogenitor cells. Plexin-B2 manipulations affect actomyosin contractility, leading to changes in cell stiffness and cytoskeletal tension, as well as cell-cell and cell-matrix adhesion. We have delineated the functional domains of Plexin-B2, RAP1/2 effectors, and the signaling association with ERK1/2, calcium activation, and YAP mechanosensor, thus providing a mechanistic link between Plexin-B2-mediated cytoskeletal tension and stem cell physiology. Plexin-B2-deficient stem cells exhibit premature lineage commitment, and a balanced level of Plexin-B2 activity is critical for maintaining cytoarchitectural integrity of the developing neuroepithelium, as modeled in cerebral organoids. Our studies thus establish a significant function of Plexin-B2 in orchestrating cytoskeletal tension and cell-cell/cell-matrix adhesion, therefore solidifying the importance of collective cell mechanics in governing stem cell physiology and tissue morphogenesis.

Suggested Citation

  • Chrystian Junqueira Alves & Rafael Dariolli & Jonathan Haydak & Sangjo Kang & Theodore Hannah & Robert J. Wiener & Stefanie DeFronzo & Rut Tejero & Gabriele L. Gusella & Aarthi Ramakrishnan & Rodrigo , 2021. "Plexin-B2 orchestrates collective stem cell dynamics via actomyosin contractility, cytoskeletal tension and adhesion," Nature Communications, Nature, vol. 12(1), pages 1-23, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26296-7
    DOI: 10.1038/s41467-021-26296-7
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    1. Chen Jiang & Ahsan Javed & Laura Kaiser & Michele M. Nava & Rui Xu & Dominique T. Brandt & Dandan Zhao & Benjamin Mayer & Javier Fernández-Baldovinos & Luping Zhou & Carsten Höß & Kovilen Sawmynaden &, 2021. "Mechanochemical control of epidermal stem cell divisions by B-plexins," Nature Communications, Nature, vol. 12(1), pages 1-17, December.
    2. Daniel A. Fletcher & R. Dyche Mullins, 2010. "Cell mechanics and the cytoskeleton," Nature, Nature, vol. 463(7280), pages 485-492, January.
    3. Zhipeng Meng & Yunjiang Qiu & Kimberly C. Lin & Aditya Kumar & Jesse K. Placone & Cao Fang & Kuei-Chun Wang & Shicong Lu & Margaret Pan & Audrey W. Hong & Toshiro Moroishi & Min Luo & Steven W. Plouff, 2018. "RAP2 mediates mechanoresponses of the Hippo pathway," Nature, Nature, vol. 560(7720), pages 655-660, August.
    4. Carsten Grashoff & Brenton D. Hoffman & Michael D. Brenner & Ruobo Zhou & Maddy Parsons & Michael T. Yang & Mark A. McLean & Stephen G. Sligar & Christopher S. Chen & Taekjip Ha & Martin A. Schwartz, 2010. "Measuring mechanical tension across vinculin reveals regulation of focal adhesion dynamics," Nature, Nature, vol. 466(7303), pages 263-266, July.
    5. Yoshiki Sasai, 2013. "Cytosystems dynamics in self-organization of tissue architecture," Nature, Nature, vol. 493(7432), pages 318-326, January.
    6. Madeline A. Lancaster & Magdalena Renner & Carol-Anne Martin & Daniel Wenzel & Louise S. Bicknell & Matthew E. Hurles & Tessa Homfray & Josef M. Penninger & Andrew P. Jackson & Juergen A. Knoblich, 2013. "Cerebral organoids model human brain development and microcephaly," Nature, Nature, vol. 501(7467), pages 373-379, September.
    7. Vedanta Mehta & Kar-Lai Pang & Daniel Rozbesky & Katrin Nather & Adam Keen & Dariusz Lachowski & Youxin Kong & Dimple Karia & Michael Ameismeier & Jianhua Huang & Yun Fang & Armando Rio Hernandez & Jo, 2020. "The guidance receptor plexin D1 is a mechanosensor in endothelial cells," Nature, Nature, vol. 578(7794), pages 290-295, February.
    8. Sean Porazinski & Huijia Wang & Yoichi Asaoka & Martin Behrndt & Tatsuo Miyamoto & Hitoshi Morita & Shoji Hata & Takashi Sasaki & S. F. Gabriel Krens & Yumi Osada & Satoshi Asaka & Akihiro Momoi & Sar, 2015. "YAP is essential for tissue tension to ensure vertebrate 3D body shape," Nature, Nature, vol. 521(7551), pages 217-221, May.
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