OUR ASSAYS COMBINE CELLULAR AND MOLECULAR BIOLOGY WITH MICROFLUIDIC FABRICATION, MICRO-PATTERNING OF PROTEINS, LIVE CELL IMAGING, HYDROGELS WITH TUNEABLE STIFFNESS AND TRACTION FORCE MICROSCOPY.

Our team studies:

  • Cellular mechanosensing (how cells sense and respond to mechanical cues from their environment)
  • How the physical properties, composition and architecture of tissues and tumors, drive cell migration and intercellular communication

Our assays combine cellular and molecular biology with microfluidic fabrication, micro-patterning of proteins, live cell imaging, hydrogels with tuneable stiffness and Traction Force Microscopy (TFM).

Using those approaches, we design novel tissue-like platforms with spatial and temporal control of cell growth, cell migration, intercellular communication, and stiffness sensing.

Our current projects focus on the following:

  • Deciphering the mechanical properties of tumor microenvironments (architecture and composition) and how this impacts cancer metastasis
  • Understanding how extracellular matrix architecture and mechanical properties impacts immune cell migration in physiological and pathological contexts
  • Implementation of on-chip devices to assess the inflammatory responses in solid tumours to test immunotherapies efficacy  

Our group strongly fosters collaborations with public and private laboratories to develop innovative fit-for-purpose multicellular drug testing platforms.

Presentation

Get to know us better

Research Staff

The people who make it all possible

Anna Labernadie 
alabernadie@cipf.es

Maria Paz Rubio Rodriguez
mprubio@cipf.es

Publications

Our scientific contributions

Targeted immunotherapy against distinct cancer-associated fibroblasts overcomes treatment resistance in refractory HER2+ breast tumors.
Rivas EI, Linares J, Zwick M, Gómez-Llonin A, Guiu M, Labernadie A, Badia-Ramentol J, Lladó A, Bardia L, Pérez-Núñez I, Martínez-Ciarpaglini C, Tarazona N, Sallent-Aragay A, Garrido M, Celià-Terrassa T, Burgués O, Gomis RR, Albanell J and Calon A
Nature Communications, 2022 Sep,  DOI:  10.1038/s41467-022-32782-3,  Vol. 13,  pag. 5310-5310

CAFs and Cancer Cells Co-Migration in 3D Spheroid Invasion Assay.
Conti S, Kato T, Park D, Sahai E, Trepat X and Labernadie A
Methods In Molecular Biology, 2021 Jan,  DOI:  10.1007/978-1-0716-0779-4_19,  Vol. 2179,  pag. 243-256

Extracellular matrix anisotropy is determined by TFAP2C-dependent regulation of cell collisions.
Park D, Wershof E, Boeing S, Labernadie A, Jenkins RP, George S, Trepat X, Bates PA and Sahai E
NATURE MATERIALS, 2020 Feb,  DOI:  10.1038/s41563-019-0504-3,  Vol. 19,  pag. 227-238

A mechanically active heterotypic E-cadherin/N-cadherin adhesion enables fibroblasts to drive cancer cell invasion.
Labernadie A, Kato T, Brugués A, Serra-Picamal X, Derzsi S, Arwert E, Weston A, González-Tarragó V, Elosegui-Artola A, Albertazzi L, Alcaraz J, Roca-Cusachs P, Sahai E and Trepat X
NATURE CELL BIOLOGY, 2017 Mar,  DOI:  10.1038/ncb3478,  Vol. 19,  pag. 224-237

Protrusion force microscopy reveals oscillatory force generation and mechanosensing activity of human macrophage podosomes.
Labernadie A, Bouissou A, Delobelle P, Balor S, Voituriez R, Proag A, Fourquaux I, Thibault C, Vieu C, Poincloux R, Charrière GM and Maridonneau-Parini I
Nature Communications, 2014 Nov,  DOI:  10.1038/ncomms6343,  Vol. 5,  pag. 5343-5343

FUNDING

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