Jordi Garcia-Ojalvo

Dr. Jordi Garcia-Ojalvo

orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 November 2005 in Nature
Verified
Journal Article
Closed access
PDF file
AAApostolos Argyris
Apostolos Argyris
DSDimitris Syvridis
Dimitris Syvridis
LLLaurent Larger
Laurent Larger
VAValerio Annovazzi-Lodi
Valerio Annovazzi-Lodi
PCPere Colet
Pere Colet
KSK. Alan Shore
K. Alan Shore

1 March 2004 in Physics Reports
Verified
Journal Article
Closed access
BLB. Lindner
B. Lindner
JGJordi Garcia-Ojalvo
Jordi Garcia-Ojalvo
ANA. Neiman
A. Neiman
LSL. Schimansky-Geier
L. Schimansky-Geier

21 October 2015 in Nature
Verified
Journal Article
Closed access
PDF file
APArthur Prindle
Arthur Prindle
JLJintao Liu
Jintao Liu
MAMunehiro Asally
Munehiro Asally
SLSan Ly
San Ly
JGJordi Garcia-Ojalvo
Jordi Garcia-Ojalvo
GSGürol M. Süel
Gürol M. Süel

23 March 2006 in Nature
Verified
Journal Article
Closed access
PDF file
GSGürol M. Süel
Gürol M. Süel
JGJordi Garcia-Ojalvo
Jordi Garcia-Ojalvo
LLLouisa M. Liberman
Louisa M. Liberman
MEMichael B. Elowitz
Michael B. Elowitz

25 April 2010 in Nature
Verified
Journal Article
Open access
PDF file
DSDavid Sprinzak
David Sprinzak
ALAmit Lakhanpal
Amit Lakhanpal
LLLauren LeBon
Lauren LeBon
LSLeah A. Santat
Leah A. Santat
MFMichelle E. Fontes
Michelle E. Fontes
MEMichael B. Elowitz
Michael B. Elowitz
The Notch–Delta signal transduction pathway is critical for many processes in development and disease, with a particular role in generating distinct cell fates among groups of initially equivalent cells and sharply defining neighbouring regions in developing tissues. Recent research has provided an increasingly comprehensive list of components and molecular interactions underlying Notch signalling, without revealing how these two proteins lead to clear cell-fate decisions. Sprinzak et al. use quantitative time-lapse microscopy to show that Notch levels in a given cell are ultrasensitive to the amount of Delta present at the surface of the same cell — as opposed to that exposed by its neighbours. This abrupt molecular switch means that a cell becomes exclusively a sender of Delta signalling (with high Delta and low Notch) or a receiver (vice versa). Numerical modelling shows how this new design principle enhances the sharpness of developmental boundaries set by classical lateral inhibition. Notch and Delta are transmembrane proteins that allow neighbouring cells to communicate during development. Here, quantitative time-lapse microscopy has been used to show that the response of Notch to Delta on a neighbouring cell is graded, whereas its response to Delta on the same cell is sharp and occurs at a fixed threshold. A mathematical model explores how this new design principle enhances the sharpness of developmental boundaries set by classical lateral inhibition. The Notch–Delta signalling pathway allows communication between neighbouring cells during development1. It has a critical role in the formation of ‘fine-grained’ patterns, generating distinct cell fates among groups of initially equivalent neighbouring cells and sharply delineating neighbouring regions in developing tissues2,3,4,5. The Delta ligand has been shown to have two activities: it transactivates Notch in neighbouring cells and cis-inhibits Notch in its own cell. However, it remains unclear how Notch integrates these two activities and how the resulting system facilitates pattern formation. Here we report the development of a quantitative time-lapse microscopy platform for analysing Notch–Delta signalling dynamics in individual mammalian cells, with the aim of addressing these issues. By controlling both cis- and trans-Delta concentrations, and monitoring the dynamics of a Notch reporter, we measured the combined cis–trans input–output relationship in the Notch–Delta system. The data revealed a striking difference between the responses of Notch to trans- and cis-Delta: whereas the response to trans-Delta is graded, the response to cis-Delta is sharp and occurs at a fixed threshold, independent of trans-Delta. We developed a simple mathematical model that shows how these behaviours emerge from the mutual inactivation of Notch and Delta proteins in the same cell. This interaction generates an ultrasensitive switch between mutually exclusive sending (high Delta/low Notch) and receiving (high Notch/low Delta) signalling states. At the multicellular level, this switch can amplify small differences between neighbouring cells even without transcription-mediated feedback. This Notch–Delta signalling switch facilitates the formation of sharp boundaries and lateral-inhibition patterns in models of development, and provides insight into previously unexplained mutant behaviours.

20 March 2013 in Reviews of Modern Physics
Verified
Journal Article
Open access
Miguel C. SorianoMiguel C. Soriano
Miguel C. Soriano
JGJordi Garcia-Ojalvo
Jordi Garcia-Ojalvo
Claudio R. MirassoClaudio R. Mirasso
Claudio R. Mirasso
IFIngo Fischer
Ingo Fischer
Complex phenomena in photonics, in particular, dynamical properties of semiconductor lasers due to delayed coupling, are reviewed. Although considered a nuisance for a long time, these phenomena now open interesting perspectives. Semiconductor laser systems represent excellent test beds for the study of nonlinear delay-coupled systems, which are of fundamental relevance in various areas. At the same time delay-coupled lasers provide opportunities for photonic applications. In this review an introduction into the properties of single and two delay-coupled lasers is followed by an extension to network motifs and small networks. A particular emphasis is put on emerging complex behavior, deterministic chaos, synchronization phenomena, and application of these properties that range from encrypted communication and fast random bit sequence generators to bioinspired information processing.