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Osteogenic Differentiation of Mesenchymal Stromal Cells: A Comparative Analysis Between Human Subcutaneous Adipose Tissue and Dental Pulp
被引:22
|作者:
D'Alimonte, Iolanda
[1
,3
,4
,5
]
Mastrangelo, Filiberto
[6
]
Giuliani, Patricia
[1
]
Pierdomenico, Laura
[2
,3
,4
,5
]
Marchisio, Marco
[2
,3
,4
,5
]
Zuccarini, Mariachiara
[1
,3
,4
]
Di Iorio, Patrizia
[1
]
Quaresima, Raimondo
[7
]
Caciagli, Francesco
[1
]
Ciccarelli, Renata
[1
,3
,4
,5
]
机构:
[1] Univ G dAnnunzio, Dept Med Oral & Biotechnol Sci, Chieti, Italy
[2] Univ G dAnnunzio, Dept Med & Aging Sci, Chieti, Italy
[3] Univ G dAnnunzio, Aging Res Ctr, Chieti, Italy
[4] Univ G dAnnunzio, Translat Med CeSI MeT, Chieti, Italy
[5] StemTeCh Grp, Chieti, Italy
[6] Vita & Salute Univ, IRCCS San Raffaele Sci Inst, Unit Dent, Milan, Italy
[7] Univ Aquila, Dept Civil Engn Architecture & Environm, Laquila, Italy
关键词:
regenerative medicine;
mesenchymal stromal cells from human subcutaneous adipose tissue (S-ASCs);
characteristics of the osteogenic differentiation of S-ASCs;
UMBILICAL-CORD BLOOD;
STEM-CELLS;
BONE-MARROW;
IN-VITRO;
PROLIFERATION;
REGENERATION;
OSTEOBLASTS;
EXPRESSION;
STRATEGIES;
THERAPY;
D O I:
10.1089/scd.2016.0190
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
White adipose tissue is a source of mesenchymal stromal/stem cells (MSCs) that are actively studied for their possible therapeutic use in bone tissue repair/remodeling. To better appreciate the osteogenic potential of these cells, we compared some properties of MSCs from human subcutaneous adipose tissue [subcutaneous-adipose stromal cells (S-ASCs)] and dental pulp stem cell (DPSCs) of third-impacted molars, the latter representing a well-established MSC source. Both undifferentiated cell types showed similar fibroblast-like morphology and mesenchymal marker expression. However, undifferentiated S-ASCs displayed a faster doubling time coupled to greater proliferation and colony-forming ability than DPSCs. Also, the osteogenic differentiation of S-ASCs was greater than that of DPSCs, as evaluated by the higher levels of expression of early osteogenic markers Runt-related transcription factor-2 (RUNX2) and alkaline phosphatase at days 3-14 and of extracellular matrix mineralization at days 14-21. Moreover, S-ASCs showed a better colonization of the titanium scaffold. In addition, we investigated whether S-ASC osteogenic commitment was enhanced by adenosine A1 receptor (A1R) stimulation, as previously shown for DPSCs. Although A1R expression was constant during DPSC differentiation, it increased in S-ASC at day 21 from osteogenesis induction. Accordingly, A1R stimulation by the agonist 2-chloro-N-6-cyclopentyladenosine, added to the cultures at each medium change, stimulated proliferation only in differentiating DPSC and enhanced the osteogenic differentiation earlier in DPSCs than in S-ASCs. These effects were counteracted by cell pretreatment with a selective A1R antagonist. Thus, our findings suggest that S-ASCs could be advantageously used in regenerative orthopedics/dentistry, and locally released or exogenously added purines may play a role in bone repair/remodeling, even though this aspect should be more thoroughly evaluated.
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页码:843 / 855
页数:13
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