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SEE INSIDE - Pittsburgh Tissue Engineering Initiative

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Preliminary Program – For full details of the Scientific Sessions check: www.regenerate-online.com<br />

WEDNESDAY - APRIL 26 continued<br />

TRACK<br />

TRACK<br />

CHAIR<br />

Cell Sourcing II<br />

Johnny Huard, PhD<br />

McGowan Institute for Regenerative Medicine<br />

<strong>Tissue</strong> <strong>Engineering</strong> & Regenerative<br />

Medicine in the Clinic (Part 1)<br />

Stephen Badylak, DVM, MD, PhD<br />

McGowan Institute for Regenerative Medicine<br />

Cell Tracking<br />

Dan Gazit, PhD, DMD<br />

The Hebrew University of Jerusalem<br />

6<br />

TRACK<br />

DESCRIPTION<br />

TRACK<br />

Presentations will include novel models for<br />

cell manipulation including mechanical<br />

stimulation and transfection. Chemical means<br />

to induce differentiation and de-differentiation<br />

will be discussed. Optimization of methods for<br />

isolation and induction of cells for research<br />

and clinical application will be presented.<br />

Embryonic Stem Cells I<br />

The subject matter of this session focuses upon the<br />

clinical translation of regenerative medicine concepts<br />

from the benchtop to the bedside and patient care. The<br />

talks cover aspects of regulatory requirements, academicindustry<br />

collaborations, third party reimbursement issues,<br />

and important clinical considerations for moving<br />

regenerative medicine into the clinic.<br />

<strong>Tissue</strong> <strong>Engineering</strong> & Regenerative<br />

Medicine in the Clinic (Part 2)<br />

Cell tracking could be a crucial issue in cell therapy and tissue<br />

engineering. Either in a systemic or local approach of cell<br />

implantation, tracking and monitoring the therapeutic cells is<br />

mandatory in order to determine:<br />

•Cell survival<br />

•Biodistribution<br />

•Cell function in tissue/organ repair (i.e. stem cell<br />

differentiation).<br />

•Cell homing and engraftment.<br />

Conventional methods of cell tracking included invasive methods<br />

that required the sacrifice of the experimental model avoiding<br />

the possibility of longitudinal, real-time monitoring of cells in vivo.<br />

Current, state-of-the-art technologies utilize genetic engineering,<br />

bioluminescence, fluorescence, nanotechnology and intra vital<br />

microscopy in order to provide non invasive, quantitative and longitudinal<br />

tracking of cells in vivo. There is no doubt that by better<br />

means of cell tracking in vivo, the field of tissue engineering<br />

would be able to better understand regeneration processes and<br />

to optimize cell-based approaches for tissue repair.<br />

Advances in Cell Culture Media<br />

TRACK<br />

CHAIR<br />

Todd McDevitt, PhD<br />

Georgia Institute of Technology and Emory University<br />

Dong-Wook Kim, PhD<br />

Yonsei University College of Medicine<br />

Stephen Badylak, DVM, MD, PhD<br />

McGowan Institute for Regenerative Medicine<br />

David Grainger, PhD<br />

Colorado State University<br />

TRACK<br />

DESCRIPTION<br />

Embryonic stem (ES) cells may serve as a<br />

pluripotent cell source for the treatment of a<br />

number of degenerative cellular diseases. This<br />

session will highlight recent advances in the<br />

derivation, cultivation and differentiation<br />

methods for ES cells, as well as the<br />

development of novel therapeutic applications<br />

of ES cells and stem cell-derived products.<br />

The subject matter of this session focuses upon the<br />

clinical translation of regenerative medicine concepts<br />

from the benchtop to the bedside and patient care. The<br />

talks cover aspects of regulatory requirements, academicindustry<br />

collaborations, third party reimbursement issues,<br />

and important clinical considerations for moving<br />

regenerative medicine into the clinic.<br />

Various deliberate and inadvertent cell culture conditions are<br />

becoming increasingly recognized for important influences<br />

on cells in culture. Different media, different serum sources,<br />

serum-free additives, and specific growth factors and hormones<br />

are soluble variables; hydrodynamic shear, oscillatory<br />

changes, and other fluid stimuli are another source of vari -<br />

ables. Full appreciation of these conditions is important to<br />

control cell phenotypic stability and regenerative destiny in<br />

cultures and bioreactors. This session provides a forum for<br />

presenting and discussing the latest thinking regarding such<br />

influences on secondary, primary and stem cell lineages.<br />

TRACK<br />

Cell-Based Sensing<br />

Pre-clinical Studies and Clinical Success:<br />

Guiding Principles (Panel Session)<br />

Cell Integration into Natural & Synthetic Matrices<br />

TRACK<br />

CHAIR<br />

William Reichert, PhD<br />

Duke University<br />

Anne Plant, PhD<br />

National Institute of Standards and Technology<br />

Kiki Hellman, PhD<br />

The Hellman Group LLC<br />

Arnold Caplan, PhD<br />

Case Western Reserve<br />

TRACK<br />

DESCRIPTION<br />

This session on cell-based biosensors examines<br />

analytical systems that employ or take<br />

advantage of detection and transduction<br />

schemes intrinsic to native cells or engineered<br />

into cells modified for analytical purposes.<br />

Particular interest is placed on<br />

approaches that are implementable in a high<br />

throughput format or that are amenable to<br />

combinatorial assay.<br />

The panel focuses on discussions and development of<br />

generic considerations for pre-clinical and clinical studies<br />

that lead to a successful therapy. Special attention is<br />

given to preclinical studies as key determinants for<br />

clinical success with focus on: clinical trial design;<br />

selection of patient profiles, i.e., inclusion/exclusion<br />

criteria; and determination of safety and effectiveness<br />

criteria and assessment measures.<br />

The principles of tissue formation and properties of<br />

natural materials can be merged to provide composite<br />

constructs used for tissue engineered regeneration of<br />

various tissues. Key issues addressed involve the use of<br />

the appropriate cells, in the proper numbers and in the<br />

optimal formulation of natural materials to organize<br />

tissue engineered regeneration.<br />

BioBlast - J.J. Collins, MD, Center for BioDynamics and the Development of Biomedical <strong>Engineering</strong>, Boston University

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