4.8 Article

Recellularization and Integration of Dense Extracellular Matrix by Percolation of Tissue Microparticles

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 35, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202103355

关键词

decellularization; extracellular matrix; hyaluronic acid-PEGDA hydrogels; microparticles; morselized; recellularization

资金

  1. DoD/CDMRP [W81XWH-20-1-0268]
  2. NIH [R01 AR063712]
  3. NSF CMMI CAREER [1349735]

向作者/读者索取更多资源

A reinforced composite material called tissue clay has been developed to mimic native tissue structure and promote tissue repair by packing acellular extracellular matrix microparticles in a hydrogel. This material can rebuild the structure of native cartilage tissue, facilitate the recellularization of chondrocytes, and show broad utility in muscle, skin, and cartilage composites.
Cells embedded in the extracellular matrix of tissues play a critical role in maintaining homeostasis while promoting integration and regeneration following damage or disease. Emerging engineered biomaterials utilize decellularized extracellular matrix as a tissue-specific support structure; however, many dense, structured biomaterials unfortunately demonstrate limited formability, fail to promote cell migration, and result in limited tissue repair. Here, a reinforced composite material of densely packed acellular extracellular matrix microparticles in a hydrogel, termed tissue clay, that can be molded and crosslinked to mimic native tissue architecture is developed. Hyaluronic acid-based hydrogels are utilized, amorphously packed with acellular cartilage tissue particulated to approximate to 125-250 microns in diameter and defined a percolation threshold of 0.57 (v/v) beyond which the compressive modulus exceeded 300 kPa. Remarkably, primary chondrocytes recellularize particles within 48 h, a process driven by chemotaxis, exhibit distributed cellularity in large engineered composites, and express genes consistent with native cartilage repair. In addition, broad utility of tissue clays through recellularization and persistence of muscle, skin, and cartilage composites in an in vivo mouse model is demonstrated. The findings suggest optimal material architectures to balance concurrent demands for large-scale mechanical properties while also supporting recellularization and integration of dense musculoskeletal and connective tissues.

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