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Notes:

allied

academies

September 10-11, 2018 | Paris, France

&

Joint Event

Otolaryngology: ENT Surgery

6

th

International Conference on

Cell & Stem Cell Research

World Congress and Expo on

Journal of Otolaryngology Online Journal | Volume 8

Homogeneous distribution of hMSC in 3D PCL scaffold by electrical stimulation

Mi Hee Lee, Min Sung Kim, Byeong-Ju Kwon, Min-Ah Koo, GyeungMi Seon, Dohyun Kim, Seung Hee Hong, Jeong Koo Kim

and

Jong-Chul Park

Yonsei University College of Medicine, Republic of Korea

T

issueengineeringhasshowntremendouspromiseincreating

biological alternatives for harvested tissues, implants, and

prostheses. An ideal scaffold for tissue regeneration should

possess large porosity and pore size for good infiltration of cells,

high pore interconnectivity for tissue ingrowth. Cell culture

in 3-D porous scaffolds is often impaired by the difficulty of

achieving a homogeneous cell seeding and by the diffusion

constraints within the cell-scaffold constructs. In the present

study, we investigated the effect of electric stimulation on

the migration of hMSCs and infiltration of hMSCs into 3D PCL

scaffold by electric stimulation. To fabricate the porous scaffold,

we simulated the current distribution in designed scaffold

using comsol physics computer program. We designed lattice

structure for difficult infiltration without any stimulation.

Then, 3D PCL scaffolds was fabricated by 3D printing. During

electrotaxis on 2D, hMSCs moved toward the anode or cathode

under direct current electric fields. Cell seeded into PCL

scaffold, incubated for 1day, and then treated 1000 μA electric

for 3h using a customized agar-salt electrotaxis chamber. After

electric current treatments, cell distribution on PCL scaffold

were visualized by immunofluorescence staining. As a result, if

there was no electric treatment, cell stayed near the surface of

scaffold. However, electric stimulation enhanced the infiltration

of cells into scaffold and hMSC distributed and proliferated

on 3D scaffolds for 28d, homogenously. In conclusion, the

infiltration of hMSCs into scaffold was enhanced by the control

ofmigrationusing physical stimulations as electrical stimulation.

Speaker Biography

Mi Hee Lee is currently pursuing in the Yonsei University College of Medicine at Republic

of Korea.

e:

parkjc@yuhs.ac

ENT and Stem Cell 2018, Volume 8

DOI: 10.4066/2250-0359-C1-003