Activin B
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Activin_B"
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The Activin dimer, from 2ARV.pdb
Identifiers
Symbol INHBA
Entrez 3624
HUGO 6066
OMIM 147290
RefSeq NM_002192
UniProt P08476
Other data
Locus Chr. 7 p15-p13
Identifiers
Symbol INHBB
Entrez 3625
HUGO 6067
OMIM 147390
RefSeq NM_002193
UniProt P09529
Other data
Locus Chr. 2 cen-q13

Activin is a peptide that enhances FSH synthesis and secretion and participates in the regulation of the menstrual cycle. It performs the opposite function from inhibin. Many other functions have been found to be exerted by activin, including their roles in cell proliferation, differentiation, apoptosis1, metabolism, homeostasis, immune response, wound repair2, and endocrine function

Like inhibin (and AMH, activin belongs to the TGF-β superfamily.

Contents

Structure

Activins are formed by the homo- or heterodimerization of activin beta subunits. In mammals, four subunits have been described called activin beta A, activin beta B, activin beta C and activin beta E. Activin beta A and beta B are identical to the two beta subunits of inhibin. A fifth subunits, activin beta D has been described in Xenopus laevis. Two activin beta A subunits give rise to activin A, one beta A and one beta B subunit gives rise to activin AB and so on. Various, but not all theoretically possible, heterodimers have been described. 3, 4

The subunits are linked by a single covalent disulfide bond.

Function

Activin is produced in the gonads, pituitary gland, placenta and other organs:

Mechanism

As with other members of the superfamily, activins interact with two types of cell surface transmembrane receptors (Types I and II) which have intrinsic serine/threonine kinase activities in their cytoplasmic domains.

Activin binds to the Type II receptor and initiates a cascade reaction that leads to the recruitment, phosphorylation, and activation of Type I activin receptor. This then interacts with and then phosphorylates SMAD2 and SMAD3, two of the cytoplasmic SMAD proteins.

Smad3 then translocates to the nucleus and interacts with SMAD4 through multimerization, resulting in their modulation as transcription factor complexes responsible for the expression of a large variety of genes.

References

  1. ^ Chen YG, Wang Q, Lin SL, Chang CD, Chung J, and Ying SY. Activin Signaling and its Role in Regulation of Cell Proliferation, Apoptosis and Carcinogenesis. Exp Biol Med. 2006; 231: 534-544.
  2. ^ Sulyok S, 20 M, Alzheimer C, Werner S. Activin: an important regulator of wound repair, fibrosis, and neuroprotection. Molecular and Cellular Endocrinology. 2005; 225: 126-132.
  3. ^ Xu P, Hall AK. The role of activin in neuropeptide induction and pain sensation. Dev Biol. 2006 Nov 15;299(2):303-9 http://www.ncbi.nlm.nih.gov/pubmed/16973148
  4. ^ Deli A, Kreidl E et al. Activins and activin antagonists in hepatocellular carcinoma. World J Gastroenterol. 2008 Mar 21;14(11):1699-709. PMID 18350601
  5. ^ Bamberger C, Schärer A, Antsiferova M, Tychsen B, Pankow S, Müller M, Rülicke T, Paus R, and Werner S. Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes. American Journal of Pathology. 2005; 167 (3): 733-741.

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