Proteomics

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Tissue and organ matrix arrays for high throughput screening and systems analysis of cell function


ABSTRACT: Cell and protein arrays have demonstrated remarkable utility in the high-throughput evaluation of biological responses; however, they lack the complexity of native tissue and organs and cannot replicate the environment of mature normal or diseased tissues. Here, we describe the development of tissue and organ extracellular matrix (ECM) arrays for screening biological outputs and systems analysis. Tissues and organs were chemically and mechanically processed and then formulated as particles without any enzymatic breakdown. The tissue ECM particles were spotted as two-dimensional tissue ECM arrays or incorporated with cells to generate three-dimensional cell-ECM microtissue arrays, and these methods were compatible with tissues prepared with varied processing techniques. The physical and biochemical properties, including the proteomic composition, of the tissue ECM arrays were characterized and compared with native tissues. The 2D arrays were validated through quantitative analysis of tissue-specific biological outputs of cell matrix production, cell adhesion and proliferation, and cell shape following culture with stem cells, cancer cells, and macrophages. Tissue-specific stem cell osteogenic differentiation on the arrays was comparable between 2D and 3D ECM environments, and revealed lung as an unexpected promoter of osteogenesis. Further gene ontology analysis of lung tissue ECM proteomics showed enrichment for families of proteins associated with skeletal development and osteogenesis. Stem cell biological outputs, along with cancer line adhesion and macrophage shape, were correlated with tissue proteomics, and network analysis identified several protein determinants of cell function. Our methodology enables broad screening of tissue and organ ECMs to connect tissue-specific composition with biological responses via systems analysis, providing a new resource for research and translation.

INSTRUMENT(S): LTQ Orbitrap Velos, Q Exactive

ORGANISM(S): Sus Scrofa Domesticus (domestic Pig)

TISSUE(S): Spleen, Cartilage, Brain, Cardiac Muscle, Liver, Lung, Bladder, Bone, Adipose Tissue, Kidney, Small Intestine

SUBMITTER: Akhilesh Pandey  

LAB HEAD: Jennifer H. Elisseeff

PROVIDER: PXD002571 | Pride | 2015-09-28

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Cornea_velos.msf Msf
ElisseeffJ_BV_1.raw Raw
ElisseeffJ_BV_1_combined.msf Msf
ElisseeffJ_BV_2.raw Raw
ElisseeffJ_BV_2_combined.msf Msf
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Publications

Tissue matrix arrays for high-throughput screening and systems analysis of cell function.

Beachley Vince Z VZ   Wolf Matthew T MT   Sadtler Kaitlyn K   Manda Srikanth S SS   Jacobs Heather H   Blatchley Michael R MR   Bader Joel S JS   Pandey Akhilesh A   Pardoll Drew D   Elisseeff Jennifer H JH  

Nature methods 20151019 12


Cell and protein arrays have demonstrated remarkable utility in the high-throughput evaluation of biological responses; however, they lack the complexity of native tissue and organs. Here we spotted tissue extracellular matrix (ECM) particles as two-dimensional (2D) arrays or incorporated them with cells to generate three-dimensional (3D) cell-matrix microtissue arrays. We then investigated the responses of human stem, cancer and immune cells to tissue ECM arrays originating from 11 different ti  ...[more]

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