Registration for a live webinar on 'Precision medicine treatment for anticancer drug resistance' is now open.
See webinar detailsWe 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
- How do cells form tissues
- From animal to molecule
- Differential adhesion is key
- Cell adhesion is key
- Epithelial architecture
- Adherens junctions mediate cell adhesion
- The cadherin-catenin complex
- Studying the process in the fruit fly
- Cell adhesion is essential
- Gastrulation illustrates the morphogenesis process
- Without adhesion gastrulation fails
- Metastasis requires loss of adhesion
- Changing the existing model of adhesion
- The dynamic events in embryogenesis
- Abl kinase and leukemia
- Abl tyrosine kinase in Drosophila
- Model of Abl in the CNS
- Abl in morphogenesis
- Dorsal closure
- Researcher Lizz Grevengoed
- Abl's role in morphogenesis
- Abl and cell shape change
- Ena is a key target of Abl in morphogenesis
- Ena and Arm co-localize at adherens junctions
- Abl regulates apical actin polymerization
- How does Abl function during complex events?
- Researcher Don Fox
- Neural tube and ventral furrow
- Apical cell constriction
- Apical constriction in action
- Wild-type ventral furrow
- Abl is required for coordinated apical constriction
- Embryos lacking functional Abl
- Models of mesoderm invagination
- Other criticl actin regulators
- Ena/VASP proteins
- Researcher Julie Gates
- The dorsal closure process
- Lammelipodia and filopodia
- Wild-type cell protrusions
- Ena and filopodia
- Ena has a key role in the formation of filopodia
- Apical-basal polarity of epithelia
- Researcher Tony Harris
- Primary landmarks of polarity
- Yeast budding as an example
- C. elegans one cell polarity
- Establishment of epithelial polarity
- AJs as primary landmarks for epithelial polarity
- Without AJs epithelial polarity is lost
- AJs as landmarks for establishing polarity
- Complex interactions among polarity determinants
- The initial establishment of polarity
- Advantages of Drosophila
- Are AJs the primary landmark?
- Baz is upstream of AJs
- Baz is normally localized in AJ mutants
- Ajs are mislocalized in baz mutants
- How is Baz positioned?
- Dynein-mediated transport
- Dynein is required for Baz positioning
- Baz/PAR3, PAR6 and aPKC
- PAR6 and aPKC apical to Baz and cadherin
- Revised model for polarity and remaining questions
- Thank you
- References
Topics Covered
- Self-assembly of cells into tissues and organs
- Understanding this process from the molecular to whole animal level
- Different cell types
- Cell adhesion
- Epithelial sheets
- Drosophila cell adhesion
- Gastrulation
- Cadherin expression
- Normal cell behavior and human disease
- Abelson tyrosine kinase
- Ena and Abl
- How does Abl function during more complex events of morphogenesis
- Other actin regulators
- Dorsal closure
- Cells use 'landmarks' to establish and elaborate polarity
- Adherens junctions
- Drosophila cellularization
- Bazooka
Talk Citation
Peifer, M. (2018, May 31). The miracle of morphogenesis, cell adhesion, polarity and cytoskeletal regulation [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/GPSN9573.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Mark Peifer has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
The miracle of morphogenesis, cell adhesion, polarity and cytoskeletal regulation
A selection of talks on Reproduction & Development
Transcript
Please wait while the transcript is being prepared...
0:00
Hi, I'm Mark Peifer from
the Department of Biology and
Lineberger Comprehensive Cancer Center
at the University of North Carolina,
Chapel Hill.
I'd like to take chance to tell you today
about some of the work from our own lab,
and how it fits together in the broader
field of the cell biology of normal
development.
0:19
Since early in my career, I've been
interested in what I view as one of
the most exciting topics in biology:
how a fertilized egg becomes an animal,
like my daughter.
This is a big problem, and in order to
study it in a single lab, one needs to
break it down into smaller problems
that one can assess experimentally.
One of the problems in which my lab is
interested is how cells self-assemble
into tissues and
organs during embryogenesis.
This is a really remarkable process,
as it's directed solely by
the genetic information and
the interactions between cells.
0:55
In order understand this process fully
we need to understand how things work at
every level of biological organization,
from the level of the entire animal,
to the level of tissue, to what
happens within individual cells, and
to the molecules that act within cells to
mediate processes like cell adhesion and
cytoskeletal regulation.
1:18
The idea that cells can specifically
recognize neighbors has been around since
the 1940s.
At that time, Holtfreter did
the experiment illustrated here.
He disassociated cells from different
embryonic tissues and mixed them, and
found that when he did so the cells could
sort out from one another, finding their
correct neighbor, and sorting from the
other neighbors of different tissue types.
We now know this results from
differential expression of cadherins
in different tissues.
Hide