A microfibril is a very fine fibril, or fiber-like strand, consisting of glycoproteins and cellulose. It is usually, but not always, used as a general term in describing the structure of protein fiber, e.g. hair and sperm tail. Its most frequently observed structural pattern is the 9+2 pattern in which two central protofibrils are surrounded by nine other pairs. Cellulose inside plants is one of the examples of non-protein compounds that are using this term with the same purpose. Cellulose microfibrils are laid down in the inner surface of the primary cell wall. As the cell absorbs water, its volume increases and the existing microfibrils separate and new ones are formed to help increase cell strength.

Synthesis and function

Cellulose is synthesized by cellulose synthase or Rosette terminal complexes which reside on a cells membrane. As cellulose fibrils are synthesized and grow extracellularly they push up against neighboring cells. Since the neighboring cell can not move easily the Rosette complex is instead pushed around the cell through the fluid phospholipid membrane. Eventually this results in the cell becoming wrapped in a microfibril layer. This layer becomes the cell wall. The organization of microfibrils forming the primary cell wall is rather disorganized. However, another mechanism is used in secondary cell walls leading to its organization. Essentially, lanes on the secondary cell wall are built with microtubules. These lanes force microfibrils to remain in a certain area while they wrap. During this process microtubules can spontaneously depolymerize and repolymerize in a different orientation. This leads to a different direction in which the cell continues getting wrapped.

Fibrillin microfibrils are found in connective tissues, which mainly makes up fibrillin-1[1] and provides elasticity. During the assembly, mirofibrils exhibit a repeating stringed-beads arrangement produced by the cross-linking of molecules forming a striated pattern with a given periodicity when viewed stained under an electron microscope. In the formation of elastic fiber, fibrillin microfibrils guides the deposit of tropoelastin and remains in the outer layer of mature elastin fibers.[2] The microfibril is also associated in cell communication. Formation of fibrillin microfibrils in the pericellular region affects the activity of a growth factor called TGFβ.[1]

Marfan syndrome

In Marfan syndrome, a connective tissue disorder, mutations in the gene encoding for the fibrillin-1 protein impact nearly every one of its domains.[3] Such defects in fibrillin-1 affect the signaling of TGFβ, as microfibrils directly govern the activity of TGFβ.[1] This hinders the formation of the extracellular matrix, and ultimately results in a severe phenotype which involves a few organ systems, including the central nervous system, circulatory system, ocular system, and skeletal system.[4]

See also

References

  1. 1 2 3 Massam-Wu, Teresa; Chiu, Maybo; Choudhury, Rawshan; Chaudhry, Shazia S.; Baldwin, Andrew K.; McGovern, Amanda; Baldock, Claire; Shuttleworth, C. Adrian; Kielty, Cay M. (2010). "Assembly of fibrillin microfibrils governs extracellular deposition of latent TGFβ" (PDF). J Cell Sci. 123 (17): 3006–3018. doi:10.1242/jcs.073437. PMC 2923573. PMID 20699357 via JCS.
  2. Kielty, Cay M.; Baldock, Claire; Lee, David; Rock, Matthew J.; Ashworth, Jane L.; Shuttleworth, C. Adrian (28 February 2002). "Fibrillin: from microfibril assembly to biomechanical function". Philos Trans R Soc Lond B Biol Sci. 357 (1148): 207–217. doi:10.1098/rstb.2001.1029. PMC 1692929. PMID 11911778.
  3. Reinhardt, Dieter P. (October–November 2014). "Microfibril-associated Disorders: Fibrillinopathies". Journal of Glaucoma. 23 (8 Suppl 1): S34-5. doi:10.1097/IJG.0000000000000114. ISSN 1057-0829. PMID 25275902. S2CID 31705597.
  4. Bonetti, Maria Ida (October 2009). "Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome". Italian Journal of Anatomy and Embryology = Archivio Italiano di Anatomia ed Embriologia. 114 (4): 201–224. ISSN 1122-6714. PMID 20578676.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.