influence of 2d and 3d environments on osteogeneic differentiation in hmscs

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Influence of 2D and 3D Environments on Osteogeneic Differentiation in hMSCs Jacqueline Mimnaugh, RET Neuqua Valley High School Dr. Richard Gemeinhart Melanie Kollmer UIC Department of Biopharmaceutical Sciences Tracy Chuong, REU University of California Berkley

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Influence of 2D and 3D Environments on Osteogeneic Differentiation in hMSCs. Jacqueline Mimnaugh , RET Neuqua Valley High School Dr. Richard Gemeinhart Melanie Kollmer UIC Department of Biopharmaceutical Sciences Tracy Chuong , REU University of California Berkley. - PowerPoint PPT Presentation

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Page 1: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

Influence of 2D and 3D Environments on Osteogeneic Differentiation in hMSCs

Jacqueline Mimnaugh, RETNeuqua Valley High School

Dr. Richard GemeinhartMelanie KollmerUIC Department of Biopharmaceutical Sciences

Tracy Chuong, REUUniversity of California Berkley

Page 2: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

Stem cells differentiate into other types of cellsTwo major categories:

What are hMSCs?

Human Mesenchymal Stem Cells (hMSCs)

Isolated from marrow

Can differentiate into bone, cartilage, fat

Embryonic(Pluripotent)

Adult(Multipotent)

Page 3: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

Induce hMSCs to develop into bone cells Osteogenesis

Tissue Engineering• Bone diseases/defects, trauma, cancer,

mal-union/non-union fractures

Why are hMSCs important?

How could we make new bone tissue for therapeutic uses?

Page 4: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

Cells in the lab are typically cultured on plates

2 D

The Problem

Cells in vivo (in an organism)

3 DIt is possible that cells grown in a 3D scaffold would:

1. Be more like cells in vivo2. Would not reach confluence as quickly3. Could be implanted directly

Page 5: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

How will a 2D and 3D environment effect the osteogenic differentiation of hMSCs?

Compare cells grown in a 2D and a 3D environment:

• Viability?• Proteins?• Genes expressed?• Mineralization?

Research Project

Page 6: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

Superporous Hydrogels

• Poly (ethylene glycol) diacrylate or PEGDA

• Polymer network, hydrophilic

• Pores from 100 µm to 600 µm created by gel-foaming

Creating a 3d Scaffold

Page 7: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

1. Seed hMSCs onto 2D plates and 3D hydrogels

Project Overview

2. Add osteogenic differentiation medium

3. Compare cells at day 2, 7, 14, 21 and 28

After 24 hours

After 24 hours

Page 8: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

1. MTS – Cell Viability

2. BCA – Protein Levels

3. Calcium

4. Alkaline Phosphatase – Early Marker

5. ELISA: Osteopontin – Early and Late MarkerOsteocalcin – Late Marker

Comparing the cells

6. qPCR – Determine Gene Expression- ALPL, RUNX2, OC, OP, BMP2

7. Von Kossa Staining - Mineralization

Page 9: Influence of 2D and 3D Environments on  Osteogeneic  Differentiation in  hMSCs

1. Seed hMSCs onto 2D plates and 3D hydrogels

Accomplished Tasks

2. Add osteogenic differentiation medium

3. Compare cells at day 2, 7, 14, 21 and 28

After 24 hours

After 24 hours

Prep: Make gels, order supplies, review protocols