Neurofilament

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neurofilament, light polypeptide 68kDa
Identifiers
Symbol NEFL
Entrez 4747
HUGO 7739
OMIM 162280
RefSeq NM_006158
UniProt P07196
Other data
Locus Chr. 8 p21
neurofilament, heavy polypeptide 200kDa
Identifiers
Symbol NEFH
Entrez 4744
HUGO 7737
OMIM 162230
RefSeq NM_021076
UniProt P12036
Other data
Locus Chr. 22 q12.1-13.1
neurofilament 3 (150kDa medium)
Identifiers
Symbol NEF3
Entrez 4741
HUGO 7734
OMIM 162250
RefSeq NM_005382
UniProt P07197
Other data
Locus Chr. 8 p21

Neurofilaments are the 10 nanometer (10nm) or intermediate filaments found specifically in neurons. The subunits of neurofilaments are related structurally to the 10nm or intermediate filaments of other tissues such as the keratin subunits, which make 10nm filaments expressed specifically in epithelia.

Classification

Class IV: NF-L, NF-M and NF-H

The family of proteins making intermediate filaments is divided into 5 major classes, the keratins forming the classes I and II. The neurofilament subunits occupy the class IV family of intermediate filaments, and was originally thought to contain only three proteins named NF-L, NF-M and NF-H.

These names come from the apparent molecular weight of the mammalian subunits on SDS-PAGE:

  • the light or lowest (NF-L) runs at 68-70kDa
  • the medium or middle (NF-M) runs at about 145-160kDa
  • the heavy or highest (NF-H) runs at 200-220kDa

The SDS-PAGE molecular weights vary between mammalian species, with larger species usually having larger proteins. Neurofilaments are found in vertebrate neurons in especially high concentrations along the axons, where they appear to regulate axonal diameter.

In the adult mammal neurofilament subunit proteins coassemble in vivo, forming a heteropolymer that contain NF-L plus NF-M or NF-H. The NF-H and NF-M proteins have lengthy C-terminal tail domains that appear to control the spacing between neighboring filaments, generating aligned arrays with a fairly uniform interfilament spacing.

Class IV: Other

A fourth class IV subunit alpha-internexin, a.k.a. NF66, is found in association with NF-L, NF-M and NF-H in many situations.

A fifth protein belonging to class IV, Nestin, is found in developing neurons and glia, and the presence of this protein is widely used to define neural stem cells. This protein is lost as development proceeds.

Class III

The class III intermediate filament protein subunit peripherin is found in neurofilaments along with the class IV subunits in a few neurons, mostly in the peripheral nervous system.

Finally another class III intermediate filament subunit, vimentin, is found in developing neurons and a few very unusual neurons in the adult in association with class IV proteins, such as the horizontal neurons of the retina.

Growth

Image:Mouse NT antibody NF Ki67.jpg
Antibody stain against Neurofilament (green) and Ki 67 (red) in a Mouse embryo 12.5 days after fertilization. The cells expressing neurofilaments are in the dorsal root ganglions shown in green while proliferating cells are in the ventricular zone in the neural tube and colored red.

During axonal growth, new neurofilament subunits are incorporated all along the axon in a dynamic process that involves the addition of subunits along the filament length, as well as the addition of subunits at the filament ends.

After an axon has grown and connected with its target cell, the diameter of the axon may increase as much as fivefold.

Neurofilaments are repulsive. This is because their purpose is to set the diameter of dendrites and axons. They do this by repelling each other because of their polarity and move away from each other.

The level of neurofilament gene expression seems to directly control axonal diameter, which in turn controls how fast electrical signals travel down the axon.[1]

See also

References

  1. http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=mboc4

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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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