Everything about Nestin Protein totally explained
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Nestin is a type VI
intermediate filament (IF) protein. These intermediate filament proteins are expressed mostly in nerve cells where they're implicated in the radial growth of the axon. Seven genes encode for the heavy (NF-H), medium (NF-M) and light neurofilament (NF-L) proteins, nestin and α-internexin in nerve cells, synemin α and desmuslin/synemin β (two alternative transcripts of the DMN gene) in muscle cells, and syncoilin (also in muscle cells). Members of this group mostly preferentially coassemble as heteropolymers in tissues. Steinert et al. has shown that nestin forms homodimers and homotetramers but doesn't form IF by itself in vitro. In mixtures, nestin preferentially co-assembles with purified vimentin or the type IV IF protein -internexin to form heterodimer coiled-coil molecules.
Gene Structure
Structurally, nestin has the shortest head domain and the longest tail domain of all the IF proteins. Nestin is of high molecular weight with a terminus greater than 500 residues (compared to cytokeratins and lamins with termini less than 50 residues).
After subcloning the human nestin gene into plasmid vectors, Dahlstrand et al.
determined the nucleotide sequence of all coding regions and parts of the introns. In order to establish the boundaries of the introns, they used the polymerase chain reaction (PCR) to amplify a fragment made from human fetal brain cDNA using two primers located in the first and fourth exon, respectively. The resulting 270 base pair (bp) long fragment was then sequenced directly in its entirety, and intron positions precisely located by comparison with the genomic sequence. Putative initiation and stop codons for the human nestin gene were found at the same positions as in the rat gene, in regions where overall similarity was very high. Based on this assumption, the human nestin gene encodes a protein with 1618 amino acids, for example 187 amino acids shorter than the rat protein.
Expression
Nestin is expressed by many types of cells during development, although its expression is usually transient and doesn't persist into adulthood. One instance of nestin expression in adult organisms, and perhaps that for which nestin is best known, are the neuronal precursor cells of the
subventricular zone. Nestin is an intermediate filament protein expressed in dividing cells during the early stages of development in the CNS, PNS and in myogenic and other tissues. Upon differentiation, nestin becomes downregulated and is replaced by tissue-specific intermediate filament proteins. During neuro- and gliogenesis, nestin is replaced by cell type-specific intermediate filaments, for example
neurofilaments and glial fibrillary acidic protein (
GFAP). Interestingly, nestin expression is reinduced in the adult during pathological situations, such as the formation of the glial scar after CNS injury and during regeneration of injured muscle tissue.
Function
Although it's utilized as a marker of proliferating and migrating cells very little is known about its functions or regulation. In depth studies on the distribution and expression of nestin in mitotically active cells indicate a complex role in regulation of the assembly and disassembly of intermediate filaments which together with other structural proteins, participate in remodeling of the cell. The role of nestin in dynamic cells, particularly structural organization of the cell, appears strictly regulated by phosphorylation, especially its integration into heterogeneous intermediate filaments together with vimentin or α -internexin. Furthermore, nestin expression has been extensively used as a marker for central nervous system (CNS) progenitor cells in different contexts, based on observations indicating a correlation between nestin expression and this cell type in vivo.
Nestin has recently received attention as a marker for detecting newly formed endothelial cells. In a study, Teranishi et al. examined and came to the conclusion that nestin is a novel angiogenesis marker of proliferating endothelial cells in colorectal cancer tissue.
Further Information
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