Literature DB >> 20967625

Lithographically defined two- and three-dimensional tissue microarrays.

Esther W Gomez1, Celeste M Nelson.   

Abstract

Traditional methods to study normal and pathological development of tissues have been limited by -difficulties in controlling experimental conditions and quantifying biological processes of interest. Here we describe methods to create microarrays of engineered tissues that enable controlled and quantitative investigations. Using soft lithography-based techniques, extracellular matrix proteins can be microcontact printed or micromolded to make two- and three-dimensional micropatterned scaffolds. The ultimate form and resulting properties of the tissue construct are dictated by the geometry of the patterned extracellular matrix components. This chapter describes elastomeric stamp fabrication, microcontact printing and micromolding of extracellular matrix proteins, cell culture in micropatterned substrata, and quantitative immunofluorescence analysis of micropatterned tissues.

Mesh:

Substances:

Year:  2011        PMID: 20967625     DOI: 10.1007/978-1-59745-551-0_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  Snail1, Snail2, and E47 promote mammary epithelial branching morphogenesis.

Authors:  Kangae Lee; Nikolce Gjorevski; Eline Boghaert; Derek C Radisky; Celeste M Nelson
Journal:  EMBO J       Date:  2011-05-24       Impact factor: 11.598

Review 2.  Microfabricated tissues for investigating traction forces involved in cell migration and tissue morphogenesis.

Authors:  Bryan A Nerger; Michael J Siedlik; Celeste M Nelson
Journal:  Cell Mol Life Sci       Date:  2016-12-22       Impact factor: 9.261

3.  PI3K regulates branch initiation and extension of cultured mammary epithelia via Akt and Rac1 respectively.

Authors:  Wenting Zhu; Celeste M Nelson
Journal:  Dev Biol       Date:  2013-05-07       Impact factor: 3.582

4.  Three-dimensional patterning of multiple cell populations through orthogonal genetic control of cell motility.

Authors:  Joanna L MacKay; Anshum Sood; Sanjay Kumar
Journal:  Soft Matter       Date:  2014-04-14       Impact factor: 3.679

5.  Transmural pressure signals through retinoic acid to regulate lung branching.

Authors:  Jacob M Jaslove; Katharine Goodwin; Aswin Sundarakrishnan; James W Spurlin; Sheng Mao; Andrej Košmrlj; Celeste M Nelson
Journal:  Development       Date:  2022-01-20       Impact factor: 6.862

6.  Cell adhesion and shape regulate TGF-beta1-induced epithelial-myofibroblast transition via MRTF-A signaling.

Authors:  Joseph W O'Connor; Esther W Gomez
Journal:  PLoS One       Date:  2013-12-10       Impact factor: 3.240

7.  Cell-cell contact and matrix adhesion promote αSMA expression during TGFβ1-induced epithelial-myofibroblast transition via Notch and MRTF-A.

Authors:  Joseph W O'Connor; Krunal Mistry; Dayne Detweiler; Clayton Wang; Esther W Gomez
Journal:  Sci Rep       Date:  2016-05-19       Impact factor: 4.379

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.