Cartilage Lacuna‐Inspired Microcarriers Drive Hyaline Neocartilage Regeneration

Author:

Ding Sheng‐Long1,Zhao Xi‐Yuan234,Xiong Wei1,Ji Lin‐Feng1,Jia Min‐Xuan234,Liu Yan‐Yan25,Guo Hai‐Tao234,Qu Feng1,Cui Wenguo6ORCID,Gu Qi234ORCID,Zhang Ming‐Zhu1ORCID

Affiliation:

1. Department of Foot and Ankle Surgery Beijing Tongren Hospital Capital Medical University Beijing 100730 P. R. China

2. State Key Laboratory of Membrane Biology Institute of Zoology Chinese Academy of Sciences Chaoyang District Beijing 100101 P. R.China

3. Beijing Institute for Stem Cell and Regenerative Medicine Chaoyang District Beijing 100101 P. R. China

4. University of Chinese Academy of Sciences Huairou District Beijing 101499 P. R. China

5. Beijing Institute of Fashion Technology Beijing 100029 P. R. China

6. Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai 200025 P. R. China

Abstract

AbstractCartilage equivalents from hydrogels containing chondrocytes exhibit excellent potential in hyaline cartilage regeneration, yet current approaches have limited success at reconstituting the architecture to culture nondifferentiated chondrocytes in vitro. In this study, specially designed lacunar hyaluronic acid microcarriers (LHAMCs) with mechanotransductive conditions that rapidly form stable hyaluronic acid (HA) N‐hydroxy succinimide ester (NHS‐ester) are reported. Specifically, carboxyl‐functionalized HA is linked to collagen type I via amide‐crosslinking, and gas foaming produced by ammonium bicarbonate forms concave surface of the microcarriers. The temporal 3D culture of chondrocytes on LHAMCs uniquely remodels the extracellular matrix to induce hyaline cartilaginous microtissue regeneration and prevents an anaerobic‐to‐aerobic metabolism transition in response to the geometric constraints. Furthermore, by inhibiting the canonical Wnt pathway, LHAMCs prevent β‐catenin translocation to the nucleus, repressing chondrocyte dedifferentiation. Additionally, the subcutaneous implantation model indicates that LHAMCs display favorable cytocompatibility and drive robust hyaline chondrocyte‐derived neocartilage formation. These findings reveal a novel strategy for regulating chondrocyte dedifferentiation. The current study paves the way for a better understanding of geometrical insight clues into mechanotransduction interaction in regulating cell fate, opening new avenues for advancing tissue engineering.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

K. C. Wong Education Foundation

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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