Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool
-
0:12 - 0:14For the past 12 years,
-
0:14 - 0:19I have been a researcher
in the field of regenerative medicine. -
0:19 - 0:21As a doctor of neuroscience,
-
0:21 - 0:24my work investigates
whether or not we can use stem cells -
0:24 - 0:28to help children who have had brain injury
or adults with spinal cord injury. -
0:30 - 0:32Today, I am going to speak with you
-
0:32 - 0:36about how we are changing
the future with stem cells. -
0:37 - 0:42I believe that stem cells
are the new Internet. -
0:43 - 0:45Think about it.
-
0:45 - 0:52Think about how the Internet completely
changed the way that we communicate, -
0:52 - 0:54the way that we do business,
-
0:54 - 0:58and even the way
that we gather data and information. -
0:58 - 1:05Similarly, I believe that stem cells
have the power to revolutionize -
1:05 - 1:08the whole concept of healthcare.
-
1:09 - 1:12So to start, let's have
a little audience participation. -
1:12 - 1:16Put your hand up: how many of you
have heard of the term "stem cells"? -
1:16 - 1:20Now leave your hand up
if you can tell me what they are. -
1:22 - 1:27This illustrates a very important part
of my work in science communications. -
1:27 - 1:30Most of us have heard
of the term stem cells -
1:30 - 1:33either through the media
or through our friends, -
1:33 - 1:36but very few of us
actually know what they are, -
1:36 - 1:40what they can do,
and, importantly, what they can't do. -
1:40 - 1:44So, today, we're going to speak
a little about what stem cells are, -
1:44 - 1:46we're going to look
at what they're currently being used for, -
1:46 - 1:49and where the future of the field lies.
-
1:50 - 1:55So, you can't be expected to understand
about stem cell treatments -
1:55 - 1:58if you don't understand
what stem cells are to begin with. -
1:58 - 2:01This is something
that I like to call "Stem Cells: 101". -
2:02 - 2:05We all know that the hundreds of cells
in the human body -
2:05 - 2:08all originate from one fertilized egg.
-
2:08 - 2:12If you think of this
as a ball rolling down a hill: -
2:12 - 2:17at the top of the hill, the ball can go
to any number of destinations downhill, -
2:17 - 2:21but as it rolls down guided by gravity,
it hits a series of forks in the road. -
2:21 - 2:25After which it must make a decision
to go one way or the other, -
2:25 - 2:29and that restricts its potential outcomes.
-
2:30 - 2:34Similarly, stem cells
during the process of differentiation -
2:34 - 2:36face a series of fate decisions
-
2:36 - 2:40where they must choose
which cell type to specialize into, -
2:40 - 2:42and they cannot go back.
-
2:43 - 2:46Near the top of the hill,
you see pluripotent stem cells: -
2:46 - 2:49"pluri-" meaning "many";
"potent", "potencies". -
2:50 - 2:53Embryonic pluripotent stem cells
-
2:53 - 2:57are the type of stem cell that people
most often associate with the word. -
2:57 - 3:03However, in reality, these cells
are virtually never used -
3:03 - 3:04in transplant paradigms.
-
3:04 - 3:09Instead, we differentiate the cell down
into multipotent progenitors -
3:09 - 3:12that are very specialized for the type
of tissue that we want to get. -
3:13 - 3:17It's important to note
that one type of multipotent cell -
3:17 - 3:19cannot make adult cells of another type.
-
3:19 - 3:24For example, fat stem cells
cannot make cells of the brain or the eye, -
3:24 - 3:26and vice versa.
-
3:27 - 3:29So, you might ask,
-
3:29 - 3:33if pluripotent stem cells can turn
into any cell in the body, -
3:33 - 3:35why don't we just inject those?
-
3:35 - 3:37You know, they could go to the site,
-
3:37 - 3:40they could travel to the site
of whatever is injured -
3:40 - 3:42and turn into the cells that we need.
-
3:43 - 3:44Right?
-
3:44 - 3:45Wrong!
-
3:45 - 3:47Because they could turn
into something like this. -
3:47 - 3:50This is called a teratoma.
-
3:50 - 3:53The problem is once we put stem cells in,
-
3:53 - 3:57we cannot control where they go
or what cells they turn into. -
3:57 - 4:00They could turn
into all of the cells in the body -
4:00 - 4:03all at once, all in the same place.
-
4:03 - 4:09Here you can see hair,
fat, tooth, gut, bone - -
4:10 - 4:14imagine if this were
in your brain or your eye. -
4:15 - 4:17This is why we must differentiate cells
-
4:17 - 4:20into the specific progenitors
as much as possible -
4:20 - 4:22before we're thinking
of transplanting them in. -
4:23 - 4:29Now, all of our adult tissue has
its own multipotent cells within it, -
4:29 - 4:34that's what helps us to grow
or when we're repairing injury, -
4:34 - 4:36and these can be harvested
in many tissues, -
4:36 - 4:40and grown in the lab
for transplanting paradigms. -
4:40 - 4:44However, there are some tissues
that you can't harvest. -
4:45 - 4:47Think about the brain
or the heart or the eye. -
4:47 - 4:50Going in there to get cells
could kill you. -
4:50 - 4:55So we have to think of other alternative
cell sources for these cells. -
4:55 - 4:58And this is where
pluripotent cells come in. -
4:58 - 5:03Now, up until now, embryonic drive cells
have been differentiated down the hill -
5:03 - 5:07into the stem cell types that we need.
-
5:08 - 5:11Recently, induced pluripotent
stem cells were developed -
5:11 - 5:15where you can take adult skin samples,
your own consenting adult, -
5:15 - 5:18push them back up the hill
using four chemical factors, -
5:18 - 5:21and then differentiate them down
to the cell type you need. -
5:21 - 5:24This was discovered recently
by Shinya Yamanaka, -
5:24 - 5:26who went on to win the Nobel Prize.
-
5:26 - 5:30The good thing about this is
it uses non embryonic sources, -
5:30 - 5:33and it's your own tissue,
so your body is not likely to reject it. -
5:33 - 5:39Alternatively, direct lineage
reprogramming - there we go - -
5:39 - 5:41takes you from A to B
-
5:41 - 5:43without this intermediate
step up the hill. -
5:43 - 5:46You can take adult skin samples
-
5:46 - 5:49and differentiate them directly
into the cell type you choose -
5:49 - 5:51using different chemical triggers.
-
5:51 - 5:55Now, this is only
in the lab phases, it's very new, -
5:55 - 5:57but it represents
a very interesting direction -
5:57 - 5:59into where the field is heading.
-
6:01 - 6:04So, what we are we doing with stem cells?
-
6:04 - 6:06Here's another audience participation.
-
6:06 - 6:11How many of you are affected by,
or know someone who has been affected by, -
6:11 - 6:12any of these diseases?
-
6:12 - 6:14Put up your hands.
-
6:14 - 6:17Stroke, burns, diabetes,
injuries to joints. -
6:18 - 6:20Now look around.
-
6:21 - 6:27Every single one of us
is affected by diseases -
6:27 - 6:31that stem cells could potentially
one day help treat. -
6:33 - 6:38Just because we are putting stem cells
into the first person in the first trial -
6:38 - 6:40doesn't mean these are a treatment,
-
6:40 - 6:43doesn't mean it's
a regular accepted treatment. -
6:43 - 6:44As you can see here,
-
6:44 - 6:47it can take up to ten years or over
-
6:47 - 6:50to get through
the clinical trials pipeline. -
6:50 - 6:52Science is incremental,
-
6:53 - 6:56but the good news is
we have a lot of treatments -
6:56 - 6:59that have been in the pipeline
for many years, -
6:59 - 7:01that are just now starting to come out.
-
7:02 - 7:05Furthermore, now more than ever before,
-
7:05 - 7:10scientists, clinicians,
members of the public, policymakers, -
7:10 - 7:15are all working together
to streamline this process. -
7:15 - 7:18That means we can get
the best stem cell treatments out -
7:18 - 7:22to the people who need them the most
in the shortest amount of time. -
7:22 - 7:25So here you see these diseases
are colour-coded -
7:25 - 7:27based on where they are on the pipeline.
-
7:27 - 7:30You can see that we have
two current treatments using stem cells -
7:30 - 7:32here in green.
-
7:32 - 7:34The first for bone and blood cancer
-
7:34 - 7:38you might know of
as a bone marrow transplant. -
7:38 - 7:40Been used for decades.
-
7:40 - 7:44The next stem cell product
to come out of the pipeline -
7:44 - 7:45is for burns and wound healing.
-
7:45 - 7:51This uses skin tissue
and helps with vision burns as well. -
7:52 - 7:55Today we're going to focus
on two major areas -
7:55 - 7:56that we're using stem cells in.
-
7:56 - 7:58The first is stroke.
-
7:58 - 8:01This is my work in childhood brain injury.
-
8:02 - 8:07Did you know that cerebral palsy
is more common -
8:07 - 8:12than juvenile AIDS, childhood leukaemia,
muscular dystrophy, -
8:12 - 8:15and juvenile diabetes combined.
-
8:16 - 8:19Cerebral palsy, which means
problems sending signals -
8:19 - 8:22from the brain to the muscles
creating movement -
8:22 - 8:26is the most common
neurodevelopmental disability. -
8:27 - 8:28What my work does,
-
8:28 - 8:31is we inject stem cells into the brain
-
8:31 - 8:36which are able to incorporate
and turn into the site types of cells -
8:36 - 8:38that are lost in the most
common forms of brain injury. -
8:38 - 8:41They can enhance function
and restore brain tissue. -
8:41 - 8:44And what my work in particular
has been able to show -
8:44 - 8:49is that we are able to functionally
double the signal speed -
8:49 - 8:51in the brains of animals.
-
8:51 - 8:54What could this mean for a child
with cerebral palsy? -
8:54 - 8:57This could mean the potential
for normal movement, -
8:57 - 9:01the ability to go out and run and jump,
to play with their friends. -
9:01 - 9:03Very exciting stuff.
-
9:03 - 9:08Right now, these cells are being used
in clinical trials only. -
9:08 - 9:11There are trials in adults
looking at stroke, -
9:11 - 9:14and there are adult trials
looking in spinal cord injury. -
9:15 - 9:18The same cells are lost in these models.
-
9:18 - 9:22Importantly, the first clinical trial
using these types of cells -
9:22 - 9:24has now started in children.
-
9:27 - 9:31Next, I want to focus
on a very interesting area -
9:31 - 9:35that's combining 3D bioprinting
with stem cell regenerative medicine. -
9:35 - 9:38This is in red, because it is
only in the early stages, -
9:38 - 9:41but I think it represents
a very exciting avenue -
9:41 - 9:43through which the field is heading.
-
9:44 - 9:47With improvements
in imaging software and technology, -
9:47 - 9:52we are now able to make accurate 3D images
-
9:52 - 9:55and take scans of body structures
inside the body. -
9:56 - 9:59Using AutoCAD and 3D software,
-
9:59 - 10:05we are able to make CAD designs
which can be printed using 3D bioprinters. -
10:05 - 10:08These bioprinters are kind of like
the printers you have at home, -
10:09 - 10:12only, instead of using ink,
they use special biogels -
10:12 - 10:15to create the structures
that you have in the body. -
10:16 - 10:20After that, you can seed them
with stem cells. -
10:20 - 10:23Here you see a heart valve being printed
-
10:23 - 10:26which can then later be seeded,
possibly with your own stem cells. -
10:27 - 10:30There's an image on the inset
of the heart valve. -
10:30 - 10:34There's also an image of an ear
being seeded with stem cells -
10:34 - 10:35which can be your own.
-
10:35 - 10:38Underneath, you see
a 3D printed image of a trachea. -
10:38 - 10:43On the bottom right, you see an interview
that I recently did with CTV national news -
10:43 - 10:48on the youngest ever
transplant recipient of a trachea -
10:48 - 10:49seeded with her own stem cells.
-
10:50 - 10:55It's important to note
that while this is very exciting, -
10:55 - 10:57it is still in its infancy.
-
10:57 - 11:00We cannot make complicated structures
with multiple cell types, -
11:01 - 11:04and right now, it is just very basic.
-
11:04 - 11:06But think about where this can head.
-
11:07 - 11:11Think about whether we could
use it in the future -
11:11 - 11:15to print structures in the body
and use our own cells for transplant. -
11:16 - 11:19So this is a very exciting field,
-
11:19 - 11:23but as with every potentially
game-changing technology, -
11:23 - 11:25there are challenges.
-
11:25 - 11:29This used to centre around the use
of embryonic drive stem cells, -
11:29 - 11:33but, recently, with the advent
of the induced pluripotent stem cells -
11:33 - 11:34and direct lineage reprogramming,
-
11:34 - 11:39which can use your own adult
consenting tissues, -
11:39 - 11:42this conversation has become
less and less relevant. -
11:43 - 11:45What we see,
-
11:45 - 11:50especially with the the increase
of treatments coming out of the pipeline, -
11:50 - 11:54is misrepresentation
of stem cell strategies. -
11:55 - 12:02Here, some doctors are offering
unproven treatments using stem cells -
12:02 - 12:04for profit.
-
12:05 - 12:09Unproven - that means
a) not proven to work, -
12:09 - 12:13and b) not proven to be safe.
-
12:14 - 12:17Recently, "Scientific American"
had an article -
12:17 - 12:22about a woman who went
to a very fancy clinic in Beverly Hills -
12:22 - 12:26and got the latest stem cell facelift
that they were offering. -
12:27 - 12:33The doctors took advantage
of a loophole in the law, -
12:34 - 12:37sucked out her fat,
and put the stem cells in her face -
12:37 - 12:41to make her rejuvenated,
or healthier or something. -
12:41 - 12:45And while they were under the hood,
they gave her dermal filler. -
12:46 - 12:50What the doctors didn't take into account
-
12:50 - 12:52is that dermal filler
-
12:52 - 12:57differentiates fat stem cells
-
12:57 - 13:00into bone.
-
13:00 - 13:05So this woman was left
with bone fragments in her eyelids. -
13:07 - 13:14This is why we need clinical trials
to make sure that treatments are safe. -
13:14 - 13:18if you were to take a drug,
and you had a bad side effect, -
13:18 - 13:22you could stop taking the drug,
and that side effect would go away. -
13:22 - 13:25But it's not the case with stem cells.
-
13:25 - 13:29Once stem cells are put in,
they can never be taken back out. -
13:30 - 13:33Furthermore, going
to an unregulated clinic -
13:33 - 13:36can exclude you
from future legitimate trials. -
13:36 - 13:40So, how do you know
whether or not what you're looking at -
13:40 - 13:44is a real stem cell treatment
or misrepresentation? -
13:44 - 13:48Here are some hints that can help you,
it's a difficult field to navigate. -
13:48 - 13:51The first: look at
how many cell types per injury. -
13:51 - 13:57We mentioned that cell types need to be
very specific to replace damaged tissue, -
13:57 - 14:01and one stem cell type
cannot turn into cells of another. -
14:01 - 14:03So it's very important if someone's saying
-
14:03 - 14:05they're going to suck out
one type of stem cell -
14:05 - 14:08and use it for 12 different indications,
-
14:08 - 14:10it's likely something you should question.
-
14:10 - 14:13Second of all: you can check out
their preclinical track record; -
14:13 - 14:16clinicaltrials. gov
is a comprehensive database -
14:16 - 14:20of all of the clinical trials
if they want to get FDA approval. -
14:21 - 14:23And the third and most important
thing that you can do -
14:23 - 14:25is to be knowledgeable.
-
14:26 - 14:29Do your research and get consensus.
-
14:30 - 14:35Ask your doctors, all of them,
because they are here to help you. -
14:37 - 14:43So, overall stem cells have the potential
-
14:43 - 14:47to change life as we know it.
-
14:48 - 14:53Every single one of us
is affected by diseases -
14:53 - 14:57which stem cells could potentially
help to treat in the future. -
14:58 - 15:03And now that you have the knowledge,
you have the power. -
15:03 - 15:07It is up to you to spread
the word about stem cells -
15:07 - 15:09and to support reputable clinical trials,
-
15:10 - 15:13so that we can work hard
to get the best treatments out -
15:13 - 15:17to the people who need them the most
in the shortest possible amount of time. -
15:18 - 15:23Right now, there are
many - more than ever before - treatments -
15:23 - 15:25in the pipeline, ready to come out.
-
15:25 - 15:29And the field of regenerative medicine
is at critical mass. -
15:30 - 15:34So I ask you to come join me
on this journey. -
15:34 - 15:40Come with me as newly-minted purveyors
of stem cell knowledge -
15:41 - 15:45as we turn science fiction
into science fact. -
15:45 - 15:46Thank you.
-
15:46 - 15:48(Applause)
- Title:
- Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool
- Description:
-
This talk was given at a TEDx event using the TED conference format but independently organized by a local community. Learn more at http://ted.com/tedx
Every single one of us is affected by diseases which stem cells could potentially treat in the future. Dr Crystal Ruff explains what stem cells are and how they are changing the way we treat diseases.
Crystal is a keen investigator in the field of regenerative neuroscience and translational health research, with a proven track record of academic and performance excellence. She concluded her MBA at the London Business School in July 2016.
Crystal's expertise lies in stem cell therapies and their transition from the lab to the clinic in order to help commercialize these strategies and get the best treatments out to the public. As a postdoctoral fellow in the Fehlings Laboratory for Neural Repair and Regeneration at the University of Toronto in Canada, she spearheaded the stem cell therapy for cerebral palsy animal initiative. Her work in knowledge translation of regenerative medicine involves several internationally-distributed documents, as well as information packages produced for the White House Office of Science & Technology Policy working group and CTV news. - Video Language:
- English
- Team:
- closed TED
- Project:
- TEDxTalks
- Duration:
- 15:59
Robert Tucker edited English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Denise RQ commented on English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Robert Tucker commented on English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Denise RQ commented on English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Robert Tucker commented on English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Denise RQ commented on English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Denise RQ edited English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool | ||
Denise RQ edited English subtitles for Changing the future with stem cells | Crystal Ruff | TEDxLondonBusinessSchool |
Denise RQ
Not sure why Note#2 (Robert's) and Note #3 (mine) aren't visible:
Thank you, Denise.
I'll just put in the capital (and not get into a long discussion about punctuation!).
Regards
Robert Tucker - 5:05 AM
Hi Robert,
Your change at 13:14 from 'if' to 'If' is correct, don't see why should, or if ever, we've gotten into a long discussion about punctuation.
Best regards and see you around.
***
Robert Tucker
All notes visible to me.
Certainly I can't always schedule whether a Harvard/Oxford comma is necessary at a certain point, or exactly which part(s) of a sentence need(s) splitting off with commas, for priority time!
Denise RQ
Not sure I can follow, Robert. There was no comment on scheduling on my part...
***
"Not sure why Note#2 (Robert's) and Note #3 (mine) aren't visible" goes to Support Team.
Robert Tucker
Sorry, Denise, I'm simply saying that some punctuation is a matter of personal preference and, unless it's something bothering someone else, not something I tend to stop and consider for too long.
Denise RQ
Dear Robert, to sum-up:
In the Amara Editor, during the approval process, I left a first note.
Note #1 is: "Great transcript, Robert! Please let me know if you have any comments or anything else is needed. Best regards,"
I noticed this note is visible, both where it was left (Amara's editor), and if you visit Yasushi's tool under 'Notes'.
***
Though I approved the task, you re-edit, and left a note for me. Your note, (note #2), said:
"Thank you, Denise.
I'll just put in the capital (and not get into a long discussion about punctuation!).
Regards".
This note #2 is only visible in the Amara editor; but not visible in the Yasushi's tool under 'Notes'. Not sure why!
And from there, much later on, I left a comment for the Support Team in my note #4.
***
To offer an answer to your note though, in the meantime, I I re-accessed the task, and left a note for you. This note, (note #3), is the following, and again(!),it is visible only in the Amara editor, but not under 'notes' in the Y's tool. Not sure why!
And that's why, much later on, I left note #4 for Support.
My note, note #3, meant for you, said:
"Hi Robert,
Your change at 13:14 from 'if' to 'If' is correct, don't see why should, or if ever, we've gotten into a long discussion about punctuation.
Best regards and see you around."
As you can re-check note #3, in my last and second note meant for you, I didn't contest your change from 'if' to 'If' (which was in fact a lowercase to a capital letter, and not a comma issue altogether), I made no other comment for you, and in fact I simply stated that 'you were right' and did an excellent job.
***
Then, much later, noticing the absence of these comments under 'notes', I left another note (note #4 in the Amara editor) and a comment in here, only for the Amara Support Team.
I hope this clarifies everything, Robert.
***
To alert Support again, I'll leave and comment on my question again: Note #4:
"Not sure why Note#2 (Robert's) and Note #3 (mine) aren't visible!
They are:
Thank you, Denise.
I'll just put in the capital (and not get into a long discussion about punctuation!).
Regards
Robert Tucker - 5:05 AM
Hi Robert,
Your change at 13:14 from 'if' to 'If' is correct, don't see why should, or if ever, we've gotten into a long discussion about punctuation.
Best regards and see you around."
Can Support offer an answer? Thanks everyone!
***