Long-term cryopreservation of dental pulp stem cells (SBP-DPSCs) and their differentiated osteoblasts: A cell source for tissue repair

被引:189
作者
Papaccio, G
Graziano, A
D'Aquino, R
Graziano, MF
Pirozzi, G
Menditti, D
De Rosa, A
Carinci, F
Laino, G
机构
[1] Secondo Ateneo Napoli, Dipartimento Med Sperimentale, Sez Istol & Embriol, Naples, Italy
[2] Secondo Ateneo Napoli, Dipartimento Discipline Odontostomatol Ortodont &, Naples, Italy
[3] Ist Nazl Tumori, UOS Dipartimentale Diagnost Mol Anal Immagine & C, Naples, Italy
[4] Univ Ferrara, Clin ORL, Cattedra Chirurg Maxillo Facciale, Arcisped S Anna, I-44100 Ferrara, Italy
关键词
D O I
10.1002/jcp.20667
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is not known whether cells derived from stem cells retain their differentiation and morpho-functional properties after long-term cryopreservation. This information is of importance to evaluate their potential for long-term storage with a view to subsequent use in therapy. Here, we describe the morpho-functional properties of dental pulp stem cells (SBP-DPSCs), and of their differentiated osteoblasts, recovered after long-term cryopreservation. After storage for 2 years, we found that stem cells are still capable of differentiation, and that their differentiated cytotypes proliferate and produce woven bone tissue. In addition, cells still express all their respective surface antigens, confirming cellular integrity. In particular, SBP-DPSCs differentiated into pre-osteoblasts, showing diffuse positivity for ALP, BAP, RUNX-2, and calcein. Recovered osteoblasts expressed bone-specific markers and were easily recognizable ultrastructurally, with no alterations observed at this level. In addition, after in vivo transplantation, woven bone converted into a 3D lamellar bone type. Therefore, dental pulp stem cells and their osteoblast-derived cells can be long-term cryopreserved and may prove to be attractive for clinical applications.
引用
收藏
页码:319 / 325
页数:7
相关论文
共 18 条
[11]   Adult stem cells for tissue repair - A new therapeutic concept? [J].
Korbling, M ;
Estrov, Z .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (06) :570-582
[12]   Viability and osteogenic potential of cryopreserved human bone marrow-derived mesenchymal cells [J].
Kotobuki, N ;
Hirose, M ;
Machida, H ;
Katou, Y ;
Muraki, K ;
Takakura, Y ;
Ohgushi, H .
TISSUE ENGINEERING, 2005, 11 (5-6) :663-673
[13]   An approachable human adult stem cell source for hard-tissue engineering [J].
Laino, G ;
Graziano, A ;
D'Aquino, R ;
Pirozzi, G ;
Lanza, V ;
Valiante, S ;
De Rosa, A ;
Naro, F ;
Vivarelli, E ;
Papaccio, G .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 206 (03) :693-701
[14]   A new population of human adult dental pulp stem cells: A useful source of living autologous fibrous bone tissue (LAB) [J].
Laino, G ;
d'Aquino, R ;
Graziano, A ;
Lanza, V ;
Carinci, F ;
Naro, F ;
Pirozzi, G ;
Papaccio, G .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (08) :1394-1402
[15]   Recovery of stem cells from cryopreserved periodontal ligament [J].
Seo, BM ;
Miura, M ;
Sonoyama, W ;
Coppe, C ;
Stanyon, R ;
Shi, S .
JOURNAL OF DENTAL RESEARCH, 2005, 84 (10) :907-912
[16]   Anabolic effects of 1,25-dihydroxyvitamin D-3 on osteoblasts are enhanced by vascular endothelial growth factor produced by osteoblasts and by growth factors produced by endothelial cells [J].
Wang, DS ;
Miura, M ;
Demura, H ;
Sato, K .
ENDOCRINOLOGY, 1997, 138 (07) :2953-2962
[17]   Fundamental cryobiology of reproductive cells and tissues [J].
Woods, EJ ;
Benson, JD ;
Agca, Y ;
Critser, JK .
CRYOBIOLOGY, 2004, 48 (02) :146-156
[18]   Identification of the haematopoietic stem cell niche and control of the niche size [J].
Zhang, JW ;
Niu, C ;
Ye, L ;
Huang, HY ;
He, X ;
Tong, WG ;
Ross, J ;
Haug, J ;
Johnson, T ;
Feng, JQ ;
Harris, S ;
Wiedemann, LM ;
Mishina, Y ;
Li, LH .
NATURE, 2003, 425 (6960) :836-841