Comprehensive Matrisome Profiling of Human Adipose Tissue for Soft Tissue Reconstruction

Author:

Major Gretel1,Simcock Jeremy2,Kumar Abhishek3,Kleffmann Torsten3,Woodfield Tim B. F.1ORCID,Lim Khoon S.14ORCID

Affiliation:

1. Department of Orthopaedic Surgery and Musculoskeletal Medicine Centre for Bioengineering & Nanomedicine University of Otago Christchurch 8011 New Zealand

2. Department of Surgery University of Otago Christchurch 8011 New Zealand

3. Centre for Protein Research Research Infrastructure Centre University of Otago Dunedin 9054 New Zealand

4. Light‐Activated Biomaterials Group School of Medical Science University of Sydney Sydney NSW 2006 Australia

Abstract

AbstractFor effective translation of research from tissue engineering and regenerative medicine domains, the cell‐instructive extracellular matrix (ECM) of specific tissues must be accurately realized. As adipose tissue is gaining traction as a biomaterial for soft tissue reconstruction, with highly variable clinical outcomes obtained, a quantitative investigation of the adipose tissue matrisome is overdue. In this study, the human adipose tissue matrisome is profiled using quantitative sequential windowed acquisition of all theoretical fragment ion spectra ‐ mass spectrometry (SWATH‐MS) proteomics across a cohort of 13 fat‐grafting patients, to provide characterization of ECM proteins within the tissue, and to understand human population variation. There are considerable differences in the expression of matrisome proteins across the patient cohort, with age and lipoaspirate collection technique contributing to the greatest variation across the core matrisome. A high abundance of basement membrane proteins (collagen IV and heparan sulfate proteoglycan) is detected, as well as fibrillar collagens I and II, reflecting the hierarchical structure of the tissue. This study provides a comprehensive proteomic evaluation of the adipose tissue matrisome and contributes to an enhanced understanding of the influence of the matrisome in adipose‐related pathologies by providing a healthy reference cohort and details an experimental pipeline that can be further exploited for future biomaterial development.

Funder

NSW Ministry of Health

Marsden Fund

Health Research Council of New Zealand

Publisher

Wiley

Subject

General Medicine

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