Tenascin

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1ten fibronectin type III

Tenascin is a protein that in humans is encoded by the TNC gene. Tenascins are a family of extracellular matrix (ECM) glycoproteins that are involved in the regulation of cellular processes such as cell adhesion, migration, and proliferation. These proteins are characterized by their ability to modulate the interaction between the cell and its microenvironment, playing a crucial role in tissue remodeling, development, and disease progression.

Structure[edit | edit source]

Tenascin is a large, multimodular glycoprotein. Its structure includes multiple domains: an assembly domain, epidermal growth factor-like repeats, fibronectin type III domains, and a fibrinogen-like globe. This complex structure allows tenascin to interact with various components of the ECM and cell surface receptors, mediating diverse biological functions.

Function[edit | edit source]

The primary function of tenascin is to modulate cell-matrix interactions. By doing so, it plays a significant role in embryonic development, influencing cell differentiation, migration, and proliferation. In adults, tenascin expression is usually low but can be upregulated in response to injury, during wound healing, and in pathological conditions such as cancer, where it contributes to the tumor microenvironment.

Isoforms[edit | edit source]

There are several isoforms of tenascin, with Tenascin-C being the most studied. These isoforms are generated through alternative splicing and have distinct expression patterns and functions. For example, Tenascin-C is prominently expressed during embryonic development and in healing wounds, whereas Tenascin-X has a more ubiquitous distribution and is involved in maintaining the structural integrity of connective tissues.

Clinical Significance[edit | edit source]

The expression of tenascin is associated with various pathological conditions. In cancer, high levels of tenascin-C are often found in the tumor microenvironment, where it can promote tumor growth, invasion, and metastasis. Additionally, mutations in the gene encoding Tenascin-X are linked to Ehlers-Danlos syndrome, a group of disorders affecting the connective tissues.

Research[edit | edit source]

Ongoing research is focused on elucidating the complex roles of tenascin in health and disease. Understanding the mechanisms by which tenascin influences cell behavior and tissue dynamics could lead to the development of novel therapeutic strategies for diseases associated with aberrant ECM remodeling, such as fibrosis, cancer, and inherited connective tissue disorders.

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Contributors: Prab R. Tumpati, MD