4.6 Article

Construction of developmentally inspired periosteum-like tissue for bone regeneration

Journal

BONE RESEARCH
Volume 10, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41413-021-00166-w

Keywords

-

Funding

  1. National Natural Science Foundation of China for Innovative Research Groups [51621002]
  2. National Key R&D Program of China [2018YFE0201500]
  3. National Natural Science Foundation of China [31870953]
  4. Foundation of Frontiers Science Center for Materiobiology and Dynamic Chemistry [JKVD1211002]
  5. Weigao Project of Chinese Academy of Sciences [(2020) 005]

Ask authors/readers for more resources

The periosteum, a highly vascularized thin tissue, has excellent osteogenic and bone regenerative abilities. Creating periosteum-like tissue using a BMP-2-loaded scaffold in vivo can be an effective strategy for bone defect repair and regeneration. The study found that BMP-2-induced endochondral ossification plays a crucial role in the construction of periosteum-like tissue.
The periosteum, a highly vascularized thin tissue, has excellent osteogenic and bone regenerative abilities. The generation of periosteum-mimicking tissue has become a novel strategy for bone defect repair and regeneration, especially in critical-sized bone defects caused by trauma and bone tumor resection. Here, we utilized a bone morphogenetic protein-2 (BMP-2)-loaded scaffold to create periosteum-like tissue (PT) in vivo, mimicking the mesenchymal condensation during native long bone development. We found that BMP-2-induced endochondral ossification plays an indispensable role in the construction of PTs. Moreover, we confirmed that BMP-2-induced PTs exhibit a similar architecture to the periosteum and harbor abundant functional periosteum-like tissue-derived cells (PTDCs), blood vessels, and osteochondral progenitor cells. Interestingly, we found that the addition of chondroitin sulfate (CS), an essential component of the extracellular matrix (ECM), could further increase the abundance and enhance the function of recruited PTDCs from the PTs and finally increase the regenerative capacity of the PTs in autologous transplantation assays, even in old mice. This novel biomimetic strategy for generating PT through in vivo endochondral ossification deserves further clinical translation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available