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Printable Handouts
Navigable Slide Index
- Introduction
- Outline of talk (1)
- Chemotactic cytokines – chemokines (1)
- Chemotactic cytokines – chemokines (2)
- Chemotaxis
- Chemokine nomenclature
- Chemokine receptor signalling (1)
- Chemokine receptor signalling (2)
- Different leukocytes express different repertoires of chemokine receptors
- The chemokine family
- Entry of leukocytes into tissues
- Leukocytes trafficking from the circulation to the tissues
- Chemokines and glycosaminoglycans (GAGs)
- Chemokines with mucin stalks
- Chemokines have other vital roles
- Atypical chemokine receptors (1)
- Atypical chemokine receptors (2)
- Outline of talk (2)
- Microbial corruption of the chemokine system (1)
- ‘Flattery that turns to battery’
- Microbial corruption of the chemokine system (2)
- Microbial corruption of the chemokine system (3)
- A 32 base pair deletion in CCR5 confers resistance to HIV-1 infection
- Subversion – SpyCEP & necrotising fasciitis
- Streptococcus pyogenes
- SpyCEP cleaves the C-terminal helix of CXCL8, impairing its chemotactic activity
- Outline of talk (3)
- Chemokines as a double edged sword
- Chemokine receptors as targets in the treatment of asthma
- CCR3 – the eotaxin receptor
- How does UCB35625 antagonise CCR3?
- UCB35625 inhibits the chemotactic response to CCL11 but not ligand binding
- How does UCB35625 work?
- Modelling the inhibition of CCL11:CCR3 by UCB35625
- Chemokine receptor crystal structures
- Models for chemokine receptor activation and antagonism
- Biased agonism at chemokine receptors: obstacles or opportunities for drug discovery?
- The hunt for chemokine receptor antagonists
- Are chemokine receptors good drug targets?
- CCR5 as a drug target
- WHIM Syndrome
- Why have antagonists failed in the clinic?
- Promiscuous GPCR antagonists
- Characterisation of broad spectrum chemokine receptor antagonists
- CCR3 is a target for age-related macular degeneration
- Acknowledgements
Topics Covered
- Chemokine classification
- Chemokine function
- Chemokine signaling
- Microbial corruption of the chemokine system
- Therapeutic blockade of chemokine receptors
Links
Series:
Categories:
Therapeutic Areas:
External Links
Talk Citation
Pease, J.E. (2022, March 9). Chemokines [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/NTNU3339.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. James E. Pease has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: The Immune System - Key Concepts and Questions
Transcript
Please wait while the transcript is being prepared...
0:00
Welcome to this
talk on chemokines.
My name is Dr. James Pease.
I'm a reader in
leukocyte biology
at the National Heart & Lung Institute at
Imperial College London, United Kingdom.
0:15
The outline of this talk on
chemokines is in three parts.
In the first part, I'm going to
talk about chemokines themselves.
I'm going to introduce their classification,
their function and their signalling.
In the second part,
I'll talk about how microbes have corrupted
the chemokines system for their own purposes.
In the third and final part,
I'll talk about work on the therapeutic blockade
of chemokine receptors in various diseases.
Let's start off by introducing chemokines and talking
about their classification, function and signalling.
0:51
The term chemokine
is a portmanteau.
It comes from the phrase
chemotactic cytokines
and defines cytokines that
drive the chemotaxis of cells.
That's principally
leukocyte migration.
Chemokines are small
soluble proteins,
typically around 8-10
kDa in molecular weight
and they adopt a
tertiary structure,
as shown here in this slide.
It's notable for the presence
of a 'greek-key' motif,
which is three anti-parallel
β pleated sheets
and the C-terminal α helix.
The structure of a chemokine is
underpinned by two disulfide bonds,
and they're typically
secreted as mature peptides
following the removal or excision
of a short signal peptide.
1:37
The family of 40 or so
chemokines in the human
can be conveniently subdivided
into four major classes,
and that's based on their arrangement
of N-terminal cysteine residues.
The majority of chemokines
fall into the families
known as the CC and
the CXC families.
CC chemokines concern an N-terminus
with two adjacent cysteine residues,
whereas the CXC chemokines have a single amino
acid interspersed between the cysteines.
There are also a couple of
minor chemokine families.
The CX_3C family contains three amino
acids between these N-terminal cysteines.
Whilst the C chemokines have a single
cysteine residue in their N-terminus.
Chemokines are predominately
quite basic molecules,
and they have several conserved
lysine and arginine residues,
notably in the C-terminus.
The primary function of chemokines
is shown on this slide here.
They drive the
chemotaxis of cells.
That can be defined as the directional migration
of a cell towards a chemical stimulus.