TY - CHAP
T1 - MSC populations for cartilage regeneration
AU - Narcisi, Roberto
AU - Cleary, Mairéad A.
AU - Sivasubramaniyan, Kavitha
AU - Brama, Pieter A.J.
AU - van Osch, Gerjo J.V.M.
N1 - Publisher Copyright: © 2017, Springer International Publishing AG. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Adult mesenchymal stem cells (MSCs) have an excellent capacity to repair tissues since they can proliferate and differentiate to form various tissues, cartilage included. Moreover, MSCs are potentially accessible in high quantities with low donor site morbidity and reasonable cartilage-forming capacity. In 1998, Johnstone et al. (Exp Cell Res 238(1):265-272) were the first that proposed an effective protocol to chondrogenically differentiate MSCs by using transforming growth factor-ß (TGF-ß), now used by many groups in the world and since then hardly changed. However, MSCs are a heterogeneous population, and the amount and type of cartilage formed are strongly influenced by intra- and inter-donor variation. In this chapter, we mainly focused on surface markers and their modulation by growth factors. We aim to first clarify the characteristics and the embryonic origin of cartilage progenitor cells (chondroprogenitor), then to summarize the characteristics and the contribution to cartilage repair by MSCs from different origins both in vivo and in vitro, and finally, to show a few examples of promoting articular cartilage phenotype by growth factor administration, in relation to the modulation of surface marker expression. With the exception of the next section focused on embryology, our interest was posed specifically on MSCs from human origin.
AB - Adult mesenchymal stem cells (MSCs) have an excellent capacity to repair tissues since they can proliferate and differentiate to form various tissues, cartilage included. Moreover, MSCs are potentially accessible in high quantities with low donor site morbidity and reasonable cartilage-forming capacity. In 1998, Johnstone et al. (Exp Cell Res 238(1):265-272) were the first that proposed an effective protocol to chondrogenically differentiate MSCs by using transforming growth factor-ß (TGF-ß), now used by many groups in the world and since then hardly changed. However, MSCs are a heterogeneous population, and the amount and type of cartilage formed are strongly influenced by intra- and inter-donor variation. In this chapter, we mainly focused on surface markers and their modulation by growth factors. We aim to first clarify the characteristics and the embryonic origin of cartilage progenitor cells (chondroprogenitor), then to summarize the characteristics and the contribution to cartilage repair by MSCs from different origins both in vivo and in vitro, and finally, to show a few examples of promoting articular cartilage phenotype by growth factor administration, in relation to the modulation of surface marker expression. With the exception of the next section focused on embryology, our interest was posed specifically on MSCs from human origin.
UR - http://www.scopus.com/inward/record.url?scp=85033703486&partnerID=8YFLogxK
U2 - 10.1007/978-3-319-53316-2_2
DO - 10.1007/978-3-319-53316-2_2
M3 - Chapter
AN - SCOPUS:85033703486
SN - 9783319533148
VL - 3
SP - 35
EP - 57
BT - Repair Strategies and Regeneration
PB - Springer International Publishing AG
ER -