We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Stem cell fate choice (1)
- Why study HSCs?
- Haematopoiesis is a hierachical process
- What constitutes a HSC?
- Spleen colony assay
- Colony forming assay
- Long-term culture
- Competition repopulation assay
- Single cell transplantation
- What have single cell assays taught us?
- HSC subtypes and leukemia
- The big problem with stem cell biology
- How do we study the properties of an HSC?
- Linking functional and transcriptional data
- Index sorting experiment
- Identification of molecular overlap
- Summary
- Stem cell fate choice (2)
- How do we study populations?
- Somatic mutations
- Assessing mutations within colonies
- HSPC family trees
- Self-renewal division can be inferred historically
- Inferred historic blood stem cell population size
- Additional questions
- Recapture experiments
- Targeted sequencing of peripheral blood
- Stability and divergence in lineages over time
- Estimating HSC population size
- Lecture summary
- What does the future hold?
- Thank you
Topics Covered
- The haematopoietic process
- Spleen colony assay
- Colony forming assay
- Competition repopulation assay
- Haematopoietic stem cell subtypes and leukemia
- Index sorting experiments and the identification of a molecular overlap
- Assessing somatic mutations within HSC colonies
- Recapture experiments
- Inferring HSC population size
Talk Citation
Kent, D. (2018, December 31). Hematopoietic stem cells: the power of clonal assays [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 3, 2024, from https://doi.org/10.69645/MFZM5895.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. David Kent has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Methods
Transcript
Please wait while the transcript is being prepared...
0:00
Hi there, my name is David Kent and I'm a group leader at
the Wellcome-MRC Cambridge Stem Cell Institute
at the University of Cambridge in the United Kingdom.
Today, I'm going to talk to you about
hematopoietic stem cells and, in particular, the power of clonal assays.
0:14
So, fundamentally, stem cells have to undergo
a series of divisions that involve a series of fate choices.
Those fate choices can very simplistically yet,
provocatively be summarized in this simple diagram.
This diagram shows where a stem cell has to decide whether or not to make a single stem cell,
which is equally capable of all the things that the stem cell is used to doing
or, a differentiated cell, which goes down and makes one of
the many different types of mature cells
in the adult cell system that the stem cell is based in.
At a population level,
this balance of fate decisions can go awry and you can get an accumulation of
either more immature leg stem cells or you can get an accumulation of
differentiated cells, which results in the depletion of these stem cells.
When you have this happen on a population level,
you end up with the result in the body of having too many immature cells situation like
cancer or, too many differentiated cells and
not enough stem cells to supply the system on a daily basis,
which is represented by tissue aging or degeneration.
Now, at a fundamental population level,
we're very interested in questions,
as scientists, about how this balance is established
and how it's maintained throughout life?
We know, fundamentally, that population asymmetry is required for homeostasis
but, when it goes wrong we want to understand,
at the stem cell level,
what the implications are for disease.
So, if we understand stem fate choice completely,
can we understand how to treat diseases of stem cell origin and can
we, indeed, try and figure out ways of supplying unlimited cell types for the body?