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Iowa Section of AADR - The University of Iowa College of Dentistry

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22. Enhancement <strong>of</strong> Rat MSC Capabilities by Intracelluar Release <strong>of</strong> Estradiol<br />

N. Benassi 1 , Y. Yu 1 , V. Joshi 1 , N. Wei 1 , A.K. Salem 1 , L. Hong 1<br />

1 <strong>University</strong> <strong>of</strong> <strong>Iowa</strong><br />

Stem cell-based bone tissue engineering has emerged as an increasingly promising alternative approach for the<br />

bone marrow-derived MSCs are considered a potentially attractive cell source for this approach, the natural<br />

population <strong>of</strong> MSC is very limited and their differentiation capabilities are easily reduced following in vitro cell<br />

expansion. Thus, it is essential to develop strategies that can be used to improve the potential utilization <strong>of</strong> MSCs<br />

for clinical application. Estrogen effectively improves MSC capabilities and has strong potential as a regulator <strong>of</strong><br />

can serve as a tool for intracellular delivery <strong>of</strong> estradiol (E2) to effectively execute estrogen regulation <strong>of</strong> MSCs.<br />

Objectives: This study is to evaluate in vitro and in vivo bone regenerative capability <strong>of</strong> MSCs with intracellular<br />

release <strong>of</strong> E2.<br />

Methods: After rat bone marrow MSCs took up E2-loaded PLGA microparticles, their proliferation and in vitro<br />

In vivo bone<br />

regeneration <strong>of</strong> these MSCs was investigated using a rat calvarial bone defect model.<br />

Results:<br />

proliferation rate compared to the controls. mRNA expression <strong>of</strong> osteocalcin, an osteogenic differentiation marker,<br />

differentiation medium in vitro. Bone regeneration at calvarial defects treated by MSCs with uptake <strong>of</strong> E2-loaded<br />

PLGA particles are faster than controls.<br />

Conclusions: Intracellular release <strong>of</strong> E2 delivered by PLGA microparticles effectively enhanced proliferation and<br />

bone regenerative capabilities <strong>of</strong> MSCs. This approach can be potentially used to improve the capabilities <strong>of</strong> MSCs<br />

for MSC-based bone tissue engineering.<br />

Supported by: <strong>University</strong> <strong>of</strong> <strong>Iowa</strong>, <strong>College</strong> <strong>of</strong> <strong>Dentistry</strong>, <strong>Iowa</strong> Dental Research Grant<br />

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