TGF beta 3

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Transforming Growth Factor Beta 3 (TGF-β3) is a member of the Transforming Growth Factor Beta (TGF-β) superfamily, which is a group of proteins known for their roles in cellular differentiation, embryonic development, regulation of the immune system, and tissue repair. TGF-β3, like other members of the TGF-β family, is involved in the communication between cells that controls a wide range of cellular processes.

Function[edit | edit source]

TGF-β3 plays a critical role in the development and maintenance of various tissues and organs. It is involved in the regulation of cell proliferation, apoptosis (programmed cell death), angiogenesis (formation of new blood vessels), and fibrosis (formation of fibrous tissue). In embryonic development, TGF-β3 is essential for the proper formation of the palate in the mouth, and mutations in the gene encoding TGF-β3 have been associated with cleft lip and cleft palate syndromes.

In addition to its role in development, TGF-β3 is also involved in the process of wound healing and tissue repair. It promotes the deposition of extracellular matrix and helps in the resolution of inflammation. TGF-β3's ability to regulate the immune response makes it a target of interest for therapeutic interventions in diseases characterized by excessive inflammation or fibrosis.

Gene and Protein Structure[edit | edit source]

The TGF-β3 gene is located on human chromosome 14q24.3 and consists of seven exons. The precursor protein encoded by this gene is cleaved to produce the mature TGF-β3 protein, which is a dimer consisting of two identical polypeptide chains linked by disulfide bonds. The mature protein is secreted from cells and interacts with specific receptors on the surface of target cells, initiating a signaling cascade that leads to the activation of downstream genes involved in cellular processes.

Clinical Significance[edit | edit source]

Alterations in TGF-β3 expression or function have been implicated in a variety of human diseases. As mentioned, mutations in the TGF-β3 gene can lead to cleft lip and palate, highlighting the protein's importance in craniofacial development. In addition, abnormal TGF-β3 signaling has been observed in several types of cancer, fibrosis, and cardiovascular diseases. Due to its role in suppressing the immune response, TGF-β3 is also being studied for its potential therapeutic applications in transplantation and autoimmune diseases.

Therapeutic Applications[edit | edit source]

Given its pivotal role in tissue repair and fibrosis, TGF-β3 has been explored as a therapeutic agent in the treatment of chronic wounds and scarring. Efforts are underway to develop drugs that can modulate TGF-β3 activity, either by enhancing its positive effects on wound healing or by inhibiting its contribution to fibrotic diseases.

Research Directions[edit | edit source]

Research on TGF-β3 continues to uncover its complex roles in health and disease. Studies are focused on understanding the detailed mechanisms of TGF-β3 signaling and its interactions with other pathways in the cell. There is also interest in developing biomarkers based on TGF-β3 activity for the diagnosis and prognosis of diseases associated with its dysregulation.


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Contributors: Prab R. Tumpati, MD