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Regenerative Medicine Some success stories!
(Part-III)
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1. Applying Regenerative Medicine to Bladder
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Applying Regenerative Medicine to Bladder
  • Neurogenic bladder disorder, for example.
  • Cystoplasty a surgical treatment.
  • What we did???
  • Human bladder was engineered!

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How???
  • Perform bladder biopsy for urothelial and muscle
    cells.
  • In vitro culturing and expansion of cells.
  • Seeding of cells on a biodegradable
    bladder-shaped scaffold.
  • New organ was ready after 8 weeks.

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Regenerated bladder
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Contd
  • 5. Anastomosis
  • 6. Apply fibrin glue.
  • 7. Omental wrapping.

Anastomosis
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Omentum layer
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Omental wrapping
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Results
  • After 46 months
  • Improved function capacity of ureter.
  • Renal function was normal through out the follow
    up.
  • No metabolic complication occured.

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  • Positives
  • No immuno-suppression required!
  • Negatives
  • No immediate Reconstruction of Vascular supply.
  • Instant Oxygen and nutrients supply is by
    diffusion.
  • Inflammation before re-angiogenesis.

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2. Applying Regenerative Medicine to Upper
Airways
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2. Applying Regenerative Medicine to Upper
Airways
  • End stage bronchio-malacia in a 30 year old
    woman, for example.
  • What we did???
  • Ex- vivo bioengineering of trachea.

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How???
  • Retrieving of deceased donor trachea.
  • Decellularization.
  • Obtaining epithelial cells from bronchial mucosa.
  • Isolation of stem cells from patients bone
    marrow.
  • Differentiation of SCs into chondrocytes.
  • 4 days maturation.
  • Human trachea was used as natural scaffold.
  • Seeding with autologous epithelial cells and
    chondrocytes.
  • Implantation of construct to replace the diseased
    one.

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Trachea scaffold
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Culturing the trachea
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Results
  • After 18 months
  • Imaging showed normal architecture.
  • Patient was doing well.
  • Advantage!
  • Use of natural/ human scaffold.

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But Behave!!
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Not all offices have science fellows.
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Ethical issues
  • About
  • Moral status of the embryo for ESCs.
  • Completely Informed consent of patient required.
  • Enrollment of subjects for clinical trials.
  • Protecting the rights and welfare of human
    subjects.
  • Resource allocation cost.
  • Intellectual property considerations.

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Thanks! ?
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