Ronen Zaidel-BarManagement2019-01-11T09:48:41+08:00
Michael SHEETZ

Ronen ZAIDEL-BAR

Department of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel-Aviv University, Israel

zaidelbar@tauex.tau.ac.il

Laboratory website
Zaidel-Bar Cell Adhesion Lab

How do nascent adhesions grow into mature focal adhesions?

How do nascent adhesions grow into mature focal adhesions? Nascent adhesions undergo a transient phase of rapid assembly and disassembly through which a fraction of adhesions survive to evolve into more stable and larger [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on How do nascent adhesions grow into mature focal adhesions?

What is the role of Rho GTPases in the regulation of focal adhesion assembly?

What is the role of Rho GTPases in the regulation of focal adhesion assembly? Synergistic integrin-syndecan signaling The rate and extent of focal adhesion formation and maturation are regulated by factors such as synergistic [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on What is the role of Rho GTPases in the regulation of focal adhesion assembly?

What is the first step in focal adhesion assembly?

What is the first step in focal adhesion assembly? Focal adhesion formation is initiated upon the binding of adhesion receptors to extracellular matrix (ECM) ligands (e.g. fibronectin, vitronectin, collagen) along the cell periphery usually [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on What is the first step in focal adhesion assembly?

How do focal adhesions mature?

How do focal adhesions mature? Adhesions that manage to grow beyond the transient phase further undergo qualitative changes in a phase described as maturation. This transformation of adhesion sites into stress-fiber bound focal adhesions [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on How do focal adhesions mature?

How do focal adhesions disassemble?

How do focal adhesions disassemble? Disassembly is critical during cell spreading and forward movement to allow FAs to extend outwards towards the cell periphery [1]. Disassembly of adhesions can take place as a result [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on How do focal adhesions disassemble?

How are proteins sequentially recruited to focal adhesion sites?

How are proteins recruited to focal adhesion sites? The chronological order of protein recruitment into focal adhesions leads to the concept of sequential assembly. Accordingly, the exact composition of each elongating adhesions is dependent [...]

By Management|Nov 30th, 2023|Categories: MBInfo, Mechanosignaling|Comments Off on How are proteins sequentially recruited to focal adhesion sites?

Ronen Zaidel-Bar

Visiting Faculty

Currently Visting

6-12 Nov 2018
Office: T-Lab, Level 5

Research Areas

Cell-cell and cell-matrix adhesion, Regulation of actomyosin contractility and dynamics, C. elegans development, mechanics and molecular mechanisms of morphogenesis

Research Interests

  1. How do specific cytoskeletal proteins contribute to the organization and function of cell adhesion and actomyosin structures?
  2. How are signals processed within the “adhesome” and “contractome” to arrive at the appropriate cytoskeletal arrangement for a given cell state?
  3. How do adhesion sites and the cytoskeleton sense and respond to external mechanical forces?

Biography

Dr Zaidel-Bar obtained his Ph.D. working with Prof Benny Geiger (Weizmann Institute of Science) on the role of force in regulating cell-matrix adhesions. Their work first focused on single proteins and evolved to encompass the entire adhesome network. In his Postdoctoral training with Prof Jeff Hardin (University of Wisconsin – Madison) Dr Zaidel-Bar switched from studying cells in culture to employing the genetic model organism C. elegans for the study of cell-cell adhesions during development. Dr Zaidel-Bar was attracted to Singapore by the opening of MBI and was awarded the Singapore National Research Foundation Fellowship for promising young investigators.

Education

PhD Weizmann Institute of Science

Recent Publications

  1. Bertocchi C, Alegría JJ, Vásquez-Sepúlveda S, Ibanez-Prat R, Srinivasan A, Arrano-Valenzuela I, Castro-Pereira B, Soto-Montandon C, Trujillo-Espergel A, Montenegro-Rojas I, Deguchi S, Owen GI, Kanchanawong P, Cerda M, Motta G, Zaidel-Bar R, and Ravasio A. Systematic AI-assisted screening of the cadhesome to map epithelial monolayer mechanics. Cell Commun Signal 2026;. [PMID: 42399739]
  2. Ray S, Agarwal P, Nitzan A, Nédélec F, and Zaidel-Bar R. Actin capping protein regulates actomyosin contractility to maintain germline architecture in C. elegans. Development 2023;. [PMID: 36897576]
  3. Avivi Kela S, Sethi K, Tan PY, Suresh D, Ong HT, Castaneda PG, Amin MR, Laviv T, Cram EJ, Faix J, and Zaidel-Bar R. Tension-dependent RHGF-1 recruitment to stress fibers drives robust spermathecal tissue contraction. J Cell Biol 2022; 222(2). [PMID: 36574264]
  4. Chen Z, Oh D, Biswas KH, Zaidel-Bar R, and Groves JT. Probing the effect of clustering on EphA2 receptor signaling efficiency by subcellular control of ligand-receptor mobility. Elife 2021; 10. [PMID: 34414885]
  5. Hu S, Grobe H, Guo Z, Wang Y, Doss BL, Pan M, Ladoux B, Bershadsky AD, and Zaidel-Bar R. Reciprocal regulation of actomyosin organization and contractility in non-muscle cells by tropomyosins and alpha-actinins. Mol. Biol. Cell 2019;:mbcE19020082. [PMID: 31216217]
  6. Desai SK, Padmanabhan A, Harshe S, Zaidel-Bar R, and Kenney LJ. Salmonella biofilms program innate immunity for persistence in Caenorhabditis elegans. Proc. Natl. Acad. Sci. U.S.A. 2019;. [PMID: 31160462]
  7. Bouffard J, Cecchetelli AD, Clifford C, Sethi K, Zaidel-Bar R, and Cram EJ. The RhoGAP SPV-1 regulates calcium signaling to control the contractility of the C. elegans spermatheca during embryo transits. Mol. Biol. Cell 2019;:mbcE18100633. [PMID: 30726159]
  8. Priti A, Ong HT, Toyama Y, Padmanabhan A, Dasgupta S, Krajnc M, and Zaidel-Bar R. Syncytial germline architecture is actively maintained by contraction of an internal actomyosin corset. Nat Commun 2018; 9(1):4694. [PMID: 30410005]
  9. Agarwal P, and Zaidel-Bar R. Principles of Actomyosin Regulation In Vivo. Trends Cell Biol. 2018;. [PMID: 30385150]
  10. Chen Z, Oh D, Biswas KH, Yu C, Zaidel-Bar R, and Groves JT. Spatially modulated ephrinA1:EphA2 signaling increases local contractility and global focal adhesion dynamics to promote cell motility. Proc. Natl. Acad. Sci. U.S.A. 2018;. [PMID: 29866846]

Lab Members

Zhang Songjing

Apr 13th, 2017|Comments Off on Zhang Songjing

Alumni, Koh Group

Weng Ting

Apr 13th, 2017|Comments Off on Weng Ting

Research Associate, Koh Group

Kapish Gupta

Apr 13th, 2017|Comments Off on Kapish Gupta

Alumni, Yu Group

Ng Chan Way

Apr 13th, 2017|Comments Off on Ng Chan Way

Alumni, Yu Group

Zhou Yan

Apr 13th, 2017|Comments Off on Zhou Yan

Alumni, Yu Group

Ma Yukun

Apr 13th, 2017|Comments Off on Ma Yukun

Alumni, Yu Group

Pan Meng

Apr 11th, 2017|Comments Off on Pan Meng

Alumni, Low Group

Chen Tianchi

Apr 11th, 2017|Comments Off on Chen Tianchi

Alumni, Ladoux Group

Hayri Emrah Balcioglu

Apr 11th, 2017|Comments Off on Hayri Emrah Balcioglu

Alumni, Ladoux Group

Bryant Lee Doss

Apr 11th, 2017|Comments Off on Bryant Lee Doss

Alumni, Ladoux Group

Anand Pratap Singh

Apr 11th, 2017|Comments Off on Anand Pratap Singh

Alumni, Saunders Group, now a post-doctoral researcher at Princeton University, USA

Christopher Preveen Amourda

Apr 11th, 2017|Comments Off on Christopher Preveen Amourda

Alumni, Saunders Group

About the National University of Singapore

About NUSA leading global university centred in Asia, NUS is Singapore's flagship university, offering a global approach to education and research with a focus on Asian perspectives and expertise.

About the Mechanobiology Institute, National University of Singapore

About MBIOne of four Research Centres of Excellence at NUS, MBI is working to identify, measure and describe how the forces for motility and morphogenesis are expressed at the molecular, cellular and tissue level.
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