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
[1]   A closed system for the clinical banking of umbilical cord blood [J].
Adami, V ;
Malangone, W ;
Falasca, E ;
Marini, L ;
Risso, A ;
Crini, S ;
Toniutti, E ;
Ferraro, EP ;
Del Frate, G ;
Pittino, M ;
Biffoni, F ;
Rinaldi, C ;
Degrassi, A .
BLOOD CELLS MOLECULES AND DISEASES, 2005, 35 (03) :389-397
[2]   High-efficiency recovery of functional hematopoietic progenitor and stem cells from human cord blood cryopreserved for 15 years [J].
Broxmeyer, HE ;
Srour, EF ;
Hangoc, G ;
Cooper, S ;
Anderson, SA ;
Bodine, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (02) :645-650
[3]   Osteoblastic cells regulate the haematopoietic stem cell niche [J].
Calvi, LM ;
Adams, GB ;
Weibrecht, KW ;
Weber, JM ;
Olson, DP ;
Knight, MC ;
Martin, RP ;
Schipani, E ;
Divieti, P ;
Bringhurst, FR ;
Milner, LA ;
Kronenberg, HM ;
Scadden, DT .
NATURE, 2003, 425 (6960) :841-846
[4]   The osteoblast: A sophisticated fibroblast under central surveillance [J].
Ducy, P ;
Schinke, T ;
Karsenty, G .
SCIENCE, 2000, 289 (5484) :1501-1504
[5]   Intracellular trehalose improves the survival of cryopreserved mammalian cells [J].
Eroglu, A ;
Russo, MJ ;
Bieganski, R ;
Fowler, A ;
Cheley, S ;
Bayley, H ;
Toner, M .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :163-167
[6]   Trehalose expression confers desiccation tolerance on human cells [J].
Guo, N ;
Puhlev, I ;
Brown, DR ;
Mansbridge, J ;
Levine, F .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :168-171
[7]   Control of osteoblast function and regulation of bone mass [J].
Harada, S ;
Rodan, GA .
NATURE, 2003, 423 (6937) :349-355
[8]  
Heng BC, 2005, IN VITRO CELL DEV-AN, V41, P77
[9]  
Holt CB, 2003, CRYOLETTERS, V24, P323
[10]   Parameters of cell freezing: Implications for the cryopreservation of stem cells [J].
Hubel, A .
TRANSFUSION MEDICINE REVIEWS, 1997, 11 (03) :224-233