Intermediate filaments
Intermediate filaments are one of the three types of cytoskeletons in the cell. Their main role lies in providing
mechanical support to the cell, as well as participating in organization of the chromatin in the cell nucleus. The latter is achieved by
anchoring the chromatin to the nuclear lamina that lines the inner part of the nuclear membrane. Intermediate filaments may also be involved
in other cellular processes such as adhesion, migration and tumor invasion
(Leduc C et al, 2015). For examples of proteins localizing to the
intermediate filaments, see Figure 1. Of all human proteins, 186 (1%) have been experimentally shown to localize to
the intermediate filaments in the Cell Atlas (Figure 2). A Gene Ontology (GO)-based analysis shows molecular functions related to intermediate filament binding
and cytoskeleton structural component are highly enriched in the intermediate filament proteome. Many of the proteins localized to intermediate
filaments are also detected in additional cellular compartments, the most common ones being the cytosol and the nucleus.
The structure of the intermediate filaments
Intermediate filaments are homologous across species, and known proteins are often well studied. Unlike the other
cytoskeletons in the cell (microtubules and actin filaments),
intermediate filaments consist of non-polar filaments, which are approximately
10 nm in diameter. Although it has been demonstrated that intermediate filaments are continually undergoing a dynamic assembly/disassembly
in the cell, the mechanism of this turnover has yet to be further characterized. This dynamic remodeling is necessary for intermediate
filaments to adjust to the cell's needs, in terms of mechanical support, flexibility or attachment to the surrounding matrix
(Robert A et al, 2016).
Intermediate filament proteins are classified into subgroups, although an agreement has not yet been reached whether there are five or six
subgroups, based on their structure and homology: Keratins are categorized into type I and II (acidic and basic), whereas vimentin
(VIM), desmin
(DES), glial fibrillary acidic protein
(GFAP) and peripherin
(PRPH) are categorized as type III. Neurofilaments are categorized as
type IV and lamins as type V
(Fuchs E et al, 1994). The sixth subgroup would contain nestin
(NES) and synemin (SYNM) (Leduc C et al, 2015),
but they are often also categorized as type IV
(Robert A et al, 2016, Fuchs E et al, 1994).
For a curated list of protein markers for intermediate
filaments, see Table 1. Figure 3 shows immunofluorescent stainings of keratins in different cell types.
Table 1. Selection of proteins suitable as markers for the intermediate filaments or its substructures.
Gene |
Description |
Substructure |
KRT19
|
Keratin 19 |
Intermediate filaments |
KRT4
|
Keratin 4 |
Intermediate filaments |
DES
|
Desmin |
Intermediate filaments |
NES
|
Nestin |
Intermediate filaments |
KRT17
|
Keratin 17 |
Intermediate filaments |
KRT13
|
Keratin 13 |
Intermediate filaments |
The function of the intermediate filaments
In human cells and tissue, intermediate filaments are crucial in providing physical support and stabilizing the cell
structure, enabling them to withstand mechanical stress and tension. A subgroup of intermediate filaments,
VIM, has been shown in vitro to
exhibit different properties when exposed to increasing levels of strain. When increasing the strain the filaments are exposed to, the
structures stiffen, resisting breakage
(Janmey PA et al, 1991, Köster S et al, 2015).
There may be a dynamic rearrangement of intermediate filaments, responding to changes in cell motility, as it has been show that they are
organized closer to the nuclear membrane in immobile cells, whereas in migrating cells they are aligned with lamella in the cell's leading edge
(Leduc C et al, 2015).
There are more than 70 genes known to be coding for intermediate filaments
(Lowery J et al, 2015), and the
UniProtKB database lists approximately 200 proteins in humans as localized to the intermediate filaments. In Table 2, the 10 most highly
expressed genes coding for intermediate filament proteins are summarized.
Although most intermediate filament proteins are cytoplasmic, there is a smaller group, known as lamins, localizing to the nucleus.
In the Human Protein Atlas, nuclear lamins show staining of the nuclear membrane.
Both mutations in genes coding for cytoplasmic intermediate filaments such as keratins, as well as genes coding for nuclear lamins have been
linked to severe diseases. The review article by Herrmann et al gives an overview of the field
(Herrmann H et al, 2007).
A Gene Ontology (GO)-based analysis of the enriched genes localized to the intermediate filament proteome shows terms for both
biological processes (Figure 4a) and molecular function (Figure 4b) that are well in-line with the known functions of the intermediate filaments.
Table 2. Highly expressed single localizing intermediate filaments proteins across different cell lines.
Gene |
Description |
Average TPM |
KRT8
|
Keratin 8 |
755 |
KRT17
|
Keratin 17 |
467 |
KRT19
|
Keratin 19 |
351 |
KRT5
|
Keratin 5 |
243 |
KRT14
|
Keratin 14 |
123 |
KRT13
|
Keratin 13 |
58 |
NEFM
|
Neurofilament medium |
58 |
NES
|
Nestin |
54 |
PJA2
|
Praja ring finger ubiquitin ligase 2 |
47 |
KRT80
|
Keratin 80 |
25 |
Intermediate filament proteins with multiple locations
Approximately 67% (n=124) of the intermediate filament proteome detected in the Cell Atlas also localize to other
compartments in the cell. The cytoscape network plot (Figure 5) shows that the most common locations shared with intermediate filaments are
the nucleus and cytosol. This could possibly indicate that some of the stainings are of soluble intermediate filament subunits, that have not
assembled into filaments, or proteins that are connecting intermediate filaments to other cellular structures.
Expression levels of intermediate filament proteins in tissue
The transcriptome analysis (Figure 6) shows that intermediate filament proteins are significantly less likely to be
expressed at RNA level in all tissue types, compared to the background of all genes with protein data in the Cell Atlas. Instead, they show a
statistically significant distribution of being tissue enriched, or having mixed expression patterns. This is well in-line with the known cell
type dependent expression pattern of intermediate filaments
(Herrmann H et al, 2007).
Relevant links and publications
Fuchs E et al, 1994. Intermediate filaments: structure, dynamics, function, and disease. Annu Rev Biochem.
PubMed: 7979242 DOI: 10.1146/annurev.bi.63.070194.002021 Herrmann H et al, 2007. Intermediate filaments: from cell architecture to nanomechanics. Nat Rev Mol Cell Biol.
PubMed: 17551517 DOI: 10.1038/nrm2197 Janmey PA et al, 1991. Viscoelastic properties of vimentin compared with other filamentous biopolymer networks. J Cell Biol.
PubMed: 2007620 Köster S et al, 2015. Intermediate filament mechanics in vitro and in the cell: from coiled coils to filaments, fibers and networks. Curr Opin Cell Biol.
PubMed: 25621895 DOI: 10.1016/j.ceb.2015.01.001 Leduc C et al, 2015. Intermediate filaments in cell migration and invasion: the unusual suspects. Curr Opin Cell Biol.
PubMed: 25660489 DOI: 10.1016/j.ceb.2015.01.005 Lowery J et al, 2015. Intermediate Filaments Play a Pivotal Role in Regulating Cell Architecture and Function. J Biol Chem.
PubMed: 25957409 DOI: 10.1074/jbc.R115.640359 Robert A et al, 2016. Intermediate filament dynamics: What we can see now and why it matters. Bioessays.
PubMed: 26763143 DOI: 10.1002/bies.201500142 |