In vivo ectopic chondrogenesis of BMSCs directed by mature chondrocytes - PubMed (original) (raw)
In vivo ectopic chondrogenesis of BMSCs directed by mature chondrocytes
Xia Liu et al. Biomaterials. 2010 Dec.
Abstract
In vivo niche plays an important role in determining the fate of exogenously implanted stem cells. Due to the lack of a proper chondrogenic niche, stable ectopic chondrogenesis of mesenchymal stem cells (MSCs) in subcutaneous environments remains a great challenge. The clinical application of MSC-regenerated cartilage in repairing defects in subcutaneous cartilage such as nasal or auricular cartilage is thus severely limited. The creation of a chondrogenic niche in subcutaneous environments is the key to solving this problem. The current study demonstrates that bone marrow stromal cells (BMSCs) could form cartilage-like tissue in a subcutaneous environment when co-transplanted with articular chondrocytes, indicating that chondrocytes could create a chondrogenic niche to direct chondrogenesis of BMSCs. Then, a series of in vitro co-culture models revealed that it was the secretion of soluble factors by chondrocytes but not cell-cell contact that provided the chondrogenic signals. The subsequent studies further demonstrated that multiple factors currently used for chondroinduction (including TGF-β1, IGF-1 and BMP-2) were present in the supernatant of chondrocyte-engineered constructs. Furthermore, all of these factors were required for initiating chondrogenic differentiation and fulfilled their roles in a coordinated way. These results suggest that paracrine signaling of soluble chondrogenic factors provided by chondrocytes was an important mechanism in directing the in vivo ectopic chondrogenesis of BMSCs. The multiple co-culture systems established in this study provide new methods for directing committed differentiation of stem cells as well as new in vitro models for studying differentiation mechanism of stem cells determined by a tissue-specific niche.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Similar articles
- Xenogeneic chondrocytes promote stable subcutaneous chondrogenesis of bone marrow-derived stromal cells.
Xue K, Zhu Y, Zhang Y, Chiang C, Zhou G, Liu K. Xue K, et al. Int J Mol Med. 2012 Feb;29(2):146-52. doi: 10.3892/ijmm.2011.830. Epub 2011 Nov 7. Int J Mol Med. 2012. PMID: 22075849 - [Potential of chondrogenesis of bone marrow stromal cells co-cultured with chondrocytes on biodegradable scaffold: in vivo experiment with pigs and mice].
Liu X, Zhou GD, Lü XJ, Liu TY, Zhang WJ, Liu W, Cao YL. Liu X, et al. Zhonghua Yi Xue Za Zhi. 2007 Jul 17;87(27):1929-33. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17923021 Chinese. - Stable subcutaneous cartilage regeneration of bone marrow stromal cells directed by chondrocyte sheet.
Li D, Zhu L, Liu Y, Yin Z, Liu Y, Liu F, He A, Feng S, Zhang Y, Zhang Z, Zhang W, Liu W, Cao Y, Zhou G. Li D, et al. Acta Biomater. 2017 May;54:321-332. doi: 10.1016/j.actbio.2017.03.031. Epub 2017 Mar 22. Acta Biomater. 2017. PMID: 28342879 - [Potential seeding cells for cartilage tissue engineering--bone marrow stromal stem cells].
Kong QQ, Xiang Z, Yang ZM. Kong QQ, et al. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2002 Jul;16(4):277-80. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2002. PMID: 12181798 Review. Chinese. - TGF-β1 regulates differentiation of bone marrow mesenchymal stem cells.
Zhao L, Hantash BM. Zhao L, et al. Vitam Horm. 2011;87:127-41. doi: 10.1016/B978-0-12-386015-6.00042-1. Vitam Horm. 2011. PMID: 22127241 Review.
Cited by
- Three-Dimensional Bioprinting Scaffolding for Nasal Cartilage Defects: A Systematic Review.
Chiesa-Estomba CM, Aiastui A, González-Fernández I, Hernáez-Moya R, Rodiño C, Delgado A, Garces JP, Paredes-Puente J, Aldazabal J, Altuna X, Izeta A. Chiesa-Estomba CM, et al. Tissue Eng Regen Med. 2021 Jun;18(3):343-353. doi: 10.1007/s13770-021-00331-6. Epub 2021 Apr 17. Tissue Eng Regen Med. 2021. PMID: 33864626 Free PMC article. Review. - Engineered nasal cartilage by cell homing: a model for augmentative and reconstructive rhinoplasty.
Mendelson A, Ahn JM, Paluch K, Embree MC, Mao JJ. Mendelson A, et al. Plast Reconstr Surg. 2014 Jun;133(6):1344-1353. doi: 10.1097/PRS.0000000000000232. Plast Reconstr Surg. 2014. PMID: 24867716 Free PMC article. - Crosstalk Between Mesenchymal Stromal Cells and Chondrocytes: The Hidden Therapeutic Potential for Cartilage Regeneration.
Brose TZ, Kubosch EJ, Schmal H, Stoddart MJ, Armiento AR. Brose TZ, et al. Stem Cell Rev Rep. 2021 Oct;17(5):1647-1665. doi: 10.1007/s12015-021-10170-6. Epub 2021 May 5. Stem Cell Rev Rep. 2021. PMID: 33954877 Review. - Coculture strategies in bone tissue engineering: the impact of culture conditions on pluripotent stem cell populations.
Janardhanan S, Wang MO, Fisher JP. Janardhanan S, et al. Tissue Eng Part B Rev. 2012 Aug;18(4):312-21. doi: 10.1089/ten.TEB.2011.0681. Epub 2012 Jul 9. Tissue Eng Part B Rev. 2012. PMID: 22655979 Free PMC article. Review. - Stem cells catalyze cartilage formation by neonatal articular chondrocytes in 3D biomimetic hydrogels.
Lai JH, Kajiyama G, Smith RL, Maloney W, Yang F. Lai JH, et al. Sci Rep. 2013 Dec 19;3:3553. doi: 10.1038/srep03553. Sci Rep. 2013. PMID: 24352100 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous