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Organ-specific ECM arrays for investigating cell-ECM interactions during stem cell differentiation.
Goh, Saik-Kia; Halfter, Willi; Richardson, Thomas; Bertera, Suzanne; Vaidya, Vimal; Candiello, Joe; Bradford, Mahalia; Banerjee, Ipsita.
Affiliation
  • Goh SK; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Halfter W; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Richardson T; Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Bertera S; Present address: Lonza, Houston, TX, United States of America.
  • Vaidya V; Institute of Cellular Therapeutics, Allegheny Health Network, Pittsburgh, PA, United States of America.
  • Candiello J; Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Bradford M; Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Banerjee I; Present address: RoosterBio, Inc, Frederick, MD, United States of America.
Biofabrication ; 13(1)2020 11 10.
Article in En | MEDLINE | ID: mdl-33045682
Pluripotent stem cells are promising source of cells for tissue engineering, regenerative medicine and drug discovery applications. The process of stem cell differentiation is regulated by multi-parametric cues from the surrounding microenvironment, one of the critical one being cell interaction with extracellular matrix (ECM). The ECM is a complex tissue-specific structure which is an important physiological regulator of stem cell function and fate. Recapitulating this native ECM microenvironment niche is best facilitated by decellularized tissue/organ derived ECM, which can faithfully reproduce the physiological environment with high fidelity toin vivocondition and promote tissue-specific cellular development and maturation. Recognizing the need for organ specific ECM in a 3D culture environment in driving phenotypic differentiation and maturation of hPSCs, we fabricated an ECM array platform using native-mimicry ECM from decellularized organs (namely pancreas, liver and heart), which allows cell-ECM interactions in both 2D and 3D configuration. The ECM array was integrated with rapid quantitative imaging for a systematic investigation of matrix protein profiles and sensitive measurement of cell-ECM interaction during hPSC differentiation. We tested our platform by elucidating the role of the three different organ-specific ECM in supporting induced pancreatic differentiation of hPSCs. While the focus of this report is on pancreatic differentiation, the developed platform is versatile to be applied to characterize any lineage specific differentiation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pluripotent Stem Cells / Extracellular Matrix Language: En Journal: Biofabrication Journal subject: BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pluripotent Stem Cells / Extracellular Matrix Language: En Journal: Biofabrication Journal subject: BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom