topics in (nano) biotechnology stem cell therapy lecture 7 31st march, 2004 phd course

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TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

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Page 1: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

TOPICS IN (NANO) BIOTECHNOLOGY

Stem Cell TherapyLecture 7

31st March, 2004

PhD Course

Page 2: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Stem Cells• Introduction

• Sources and types of Stem Cells

• Main Applications

• Companies in the Field

• Stem Cells for Gene Therapy

• Legal and Ethical Issues

Page 3: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

What is a stem cell?

Page 4: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

What is a Stem Cell?

• Stem cells are undifferentiated cells capable of differentiating into any kind of tissue. This morphing process can occur almost indefinitely.

• Taken from human embryos only days old, stem cells are capable of developing into any of nearly 220 cell types that make up the human body.

• When a stem cell divides, it creates a stem cell that's specialized — one that can create cells that perform specific functions, such as blood cells. It also creates an exact replica of itself.

Page 5: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

• Totipotent: have unlimited capability. Can develop to all postembryonic tissues and organs.

• Pluripotent: stem cells capable of giving rise to most tissues of an organism.

• Multipotent: stem cells that are specialized to give rise to a particular cell type.

Types of Stem Cells

Page 6: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

• Stem cells are characterized by three hallmark properties:– Pluripotent: capable of differentiating into most

cells, but incapable of forming placental tissue so cannot form a fetus

– High Proliferative Potential: theoretically, one cell can give rise to an entire organ system

– Self-Renew: can regenerate themselves so are “immortal”

Stem Cell Properties

Page 7: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Where Do Stem Cells Come From?

• Stem cells exist in different forms in both the embryo and the adult

• Embryonic stem (ES) cells are taken from blastocyst stage embryos (just a few days old and composed of few cells), of which there are about 200,000 in cryopreservation in IVF clinics

• ES cells are pluripotent and adult stem cells have more limited abilities to differentiate but can form cell types different to their own – a property known as plasticity

Page 8: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

ES cells: - spare embryos

- special purpose embryos

- cloned embryos

Adult stem cells: - adult tissue

- cadavers

Other sources: - aborted fetuses

- umbilical cords

Sources of stem cells

Page 9: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

20 years ago - mouse ES cells

1998 - James Thompson - human ES cells

Stem cell proliferation

Page 10: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Multiple embryos are produced in vitro for clinical purposes.Donated surplus embryos are used as a source of ES cells.These surplus embryos would otherwise be discarded or remain unused

How are ES Cells Generated?

Page 11: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Fertilized Embryos Are Allowed to Divide Several Times in Culture

Page 12: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Harvesting ES Cells

The blastocyst is the stage of development (~1,000 cells) at which the embryos inner cell mass (ICM) forms. It is the ICM that harbors ES cells. Stem cells exist only fleetingly at this stage of development

Page 13: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Generating an ES Cell Line

The trophoblast is removed from the embryo, the inner cell mass is isolated and, using a micropipette, ES cells are extracted and placed in tissue culture. These cells are passaged for many generations until some spontaneously form “immortal” lines

Page 14: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Generating an ES Cell Line

In vitro growing

• Growth medium

• Feeder layers

• Spontaneous differentiation

Page 15: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Differentiation

Growth factor Induces cells from

retinoic acid ectoderm

epidermal growth factor (EGF) ectoderm

bone morphogenic protein 4 (BMP4) ectoderm

basic fibroblast growth factor (bFGF) ectoderm

activin-A mesoderm

transforming growth factor-beta 1 (TGF-B1) mesoderm

hepatocyte growth factor (HGF) three germ layers

nerve growth factor (NGF) three germ layers

Page 16: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Stem Cell Therapy

• Using replacement cells to cure disease may prove to be one of the most significant advances in medicine

• Unlike current treatments that rely on surgery or drugs to modulate activities, stem cells provide a replacement for dysfunctional or degenerating tissue

• In the future, stem cells could enable the means to create entire organs that fail due to aging or disease

Page 17: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Sources

Plasticity

- Adult Central Nervous System (CNS)

- Bone marrow and blood stem cells

- Other tissues

Adult Stem Cells

Page 18: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

What tests are used for identifying adult stem cells?

• There is not a general agreement on the criteria that should be used to identify and test adult stem cells. One of the following three methods is generally used:• Labelling cells in living tissue with molecular

markers and determination of the type of cells they specialise

• Remove cells, carry out cell culture and label, transplant into different animal to see if tissues reform cells of tissue of origin

• Isolate the cells, manipulate them (growth factors/new genes) – determine what potential cells can be formed

Page 19: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Embryonic vs Adult stem cells

Embryonic Stem Cells Embryonic Stem Cells

Page 20: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Stem Cell Therapy for Tissue Replacement

Stem cells are the parent cells of every cell in the body. Under the right conditions, ES cells can be transformed into a variety of cells that make up the bone marrow, brain, muscle, skin, pancreas, and liver

Page 21: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Clinical Applications

When transplanted into an injured tissue (eg. damaged cardiac muscle following heart attack) heart cells derived from ES cells in culture can contribute to tissue regeneration in vivo

Page 22: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Other Sources of Stem Cells• Spare Embryos: leftover from IVF clinics• Special Purpose Embryos: created by IVF for the sole

purpose of extracting stem cells• Cloned Embryos: embryos can be cloned in the lab by

somatic nuclear transfer in order to harvest their stem cells

• Aborted Fetuses: can be used as a source of stem cells early in development (5-11 weeks of gestation)

• Umbilical Cords: this normally discarded tissue holds great promise as a source of blood-forming (hematopoietic) stem cells

• Adult Tissues or Organs: stem cells can be isolated from tissues of living adults during surgery (eg. hematopoietic stem cells from bone marrow)

• Cadavers: neural progenitor cells have been isolated from human brain tissue up to 20 hours after death

Page 23: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Comparing Embryonic and Adult Stem Cells

Advantages• Flexible: have the potential to make any cell• Immortal: one ES cell line can potentially supply endless

cells with defined characteristics• Easily Available: embryos from IVF clinics

Disadvantages• Difficult to Culture: the conditions for inducing tissue-

specific differentiation are poorly understood• Immunoreactivity: ES cells from another donor may be

rejected after transplantation into an incompatible recipient• Ethically controversial: embryonic sources of stem cells

are opposed by people who believe that life begins at conception even if donors give consent

Page 24: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Comparing Embryonic and Adult Stem Cells

Advantages• Already Somewhat Specialized: inducement may be simpler• Not Immunogenic: recipients who receive the products of

their own stem cells will not experience immune rejection• Mixed Degree of Availability: some adult stem cells are easy

to harvest (skin, muscle, marrow), while others may be dangerous to the donor (brain stem cells)

Disadvantages• Limited Quantity: difficult to obtain in large numbers• Finite: don’t live as long as ES cells in culture• Less Flexible: may be more difficult to reprogram to form

other tissue types• Genetically Unsuitable: may carry genetic mutations of

disease or become defective during culture

Page 25: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

How do we turn on stem cells?

The recent discovery of molecular switches that help determine whether stem cells will become muscle cells or other cell types might pave the way for effective treatments of muscular dystrophy (MD).

Rudnicki believes Pax7 acts as a switch that tells muscle stem cells to become satellite cells instead of blood cells. If turning on Pax7 can force the cells to make this choice, it could be used to devise treatments for MD that effectively combine gene therapy with stem cell transplantation.

Page 26: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Target Diseases for Stem Cell TherapyBlood Diseases• Bone marrow transplants (BMT) are a well known clinical

application of hematopoietic stem cell (HSC) therapy• HSCs can regenerate all of the different cell types in blood• BMT is used for the treatment of blood cancers like leukemia

and lymphoma, as well as breast cancer and any other disease requiring immune system regeneration

Page 27: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Target Diseases for Stem Cell TherapyHeart Disease• ES cells can be induced to form cardiac muscle cells that

actually beat in culture• When transplanted into damaged hearts, these cells can form

gap junctions and contract in unison with surrounding cells• HSCs can also be grafted into damaged heart muscle and, in

this new environment, are reprogrammed to produce heart cells instead of blood cells

Page 28: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Target Diseases for Stem Cell TherapyBrain and Spinal Cord Injury• Neural stem cells can be isolated from

adult brains or generated from ES cells in culture

• HSCs can also be transplanted into the brain where they are reprogrammed to generate neurons and glial cells

• Potential applications include Parkinson’s disease, ALS, Huntington’s disease, stroke, Alzheimer’s disease, paralysis

• Animal and early human trials are underway

Page 29: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Target Diseases for Stem Cell Therapy

Type 1 Diabetes• Patients lack pancreatic beta cells

and cannot produce insulin• Insulin-producing structures similar

to pancreatic islets have been generated from mouse ES cells in culture

• It may also be possible to isolate pancreatic stem cells from adult tissue

• Early stage of development

Page 30: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Target Diseases for Stem Cell TherapySkin and Hair Replacement• Skin (keratinocyte) stem cells reside in the hair

follicle and can be removed when a hair is plucked

• These cells are bipotent, forming hair and epidermis in culture

• Provide tissue for autografting, without problems of immune rejection

• Clinical trials underway for venous ulcers, burn injury, and hair transplants

Page 31: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

HOW STEM CELLS AND GENE THERAPY MIGHT WORK TOGETHER

1. A sample of bone marrow is removed.

2. Stem cells are isolated and allowed to multiply in culture.

3. Cells are treated with a modified virus containing a therapeutic gene

           

Page 32: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

HOW STEM CELLS AND GENE THERAPY MIGHT WORK TOGETHER

1. The virus is taken up by individual cells and the therapeutic gene goes into the cell's nucleus.

2. Treated ("corrected") cells are injected into the bloodstream.

3. Treated cells respond to injury signals from degenerating muscle or other tissues and migrate out of the bloodstream.

4. Treated cells patch damage and build healthy tissue

              

     

             

             

          

                    

Page 33: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Stem cells for Gene Therapy

Page 34: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Commercial Opportunities in Stem Cell Research

• Devices: manufacture of equipment and materials needed to isolate stem cells from adult tissues (e.g. Antibodies, affinity beads and flasks, columns, cell sorters, etc.)

• Isolation: novel “processes” are patentable • Composition: the make-up of the isolated stem cell

product is patentable, irregardless of how it was obtained

• Manipulation: novel methods of culturing or reprogramming stem cells are patentable

Page 35: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

• Aastrom

• Advanced Cell Tech.

• BresaGen

• Cryo Cell

• Curis

• Diacrin

• Geron

• ReNeuron

• StemCells

• Incara

• Nexell

• NeuroNova

• Novartis

• Genzyme

• Others

Biotechnology Companies in the Stem Cell Field

Page 36: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Biotechnology Companies in the Stem Cell Field

Nexell

Isolex 300i Magnetic Cell Selection System. The only FDA approved device for clinical scale isolation of hematopoietic stem cells from blood

Aastrom

Manufacture a “bioreactor” that allows the growth of many hematopoietic stem cells from the small number that can typically be harvested from adult or umbilical cord blood

Page 37: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Biotechnology Companies in the Stem Cell Field

StemCells Inc.

Have parallel programs in pre-clinical development for the isolation and characterization of neural, liver and pancreatic stem cells. Primarily process and compositional patents

Geron

Own the intellectual property used to clone “Dolly” the sheep. Funded the University of Wisconsin research that generated the first human ES cells. Parallel programs in directing the development of ES cells into neural, liver and cardiac cells for transplantation

Page 38: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Biotechnology Companies in the Stem Cell Field

Diacrin

Developing xenotransplants using fetal pig cells in chronic stroke patients

NeuroNova

Strategy is to isolate adult brain stem cells, induce them to form dopaminergic neurons in culture, and then transplant these cells into the brain of patients with Parkinson’s disease

Page 39: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Biotechnology Companies in the Stem Cell Field

ReNeuronHas developed neural stem cell lines from different

regions of the human brain. Can be grown in large numbers for transplantation.

Also examining the genes and proteins expressed in neural stem cells to identify novel targets for drug discovery

NovartisThrough its acquisition of SyStemix, Inc., now owns the

composition patent on human hematopoietic stem cells

Page 40: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Ethical debate

• Harvesting ES cells destroys the blastocyst

• “This is murder”

Page 41: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Ethical debate

• ES cell research requires human cells

• Could create a commercial market for human cells

• “This devalues life”

Page 42: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Ethical debate

• “If excess IVF embryos are being discarded anyway, they should be put to good use”

Page 43: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Ethical debate

• “Therapeutic cloning is a slippery slope - it will lead to reproductive cloning”

Page 44: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Governing ES cell research

Page 45: TOPICS IN (NANO) BIOTECHNOLOGY Stem Cell Therapy Lecture 7 31st March, 2004 PhD Course

Legal & Ethical IssuesReNeuronHas developed neural stem cell lines from different

regions of the human brain. Can be grown in large numbers for transplantation.

Also examining the genes and proteins expressed in neural stem cells to identify novel targets for drug discovery

NovartisThrough its acquisition of SyStemix, Inc., now owns the

composition patent on human hematopoietic stem cells