Contactin 2

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Contactin 2, also known as CNTN2 or TAG-1 (Transient Axonal Glycoprotein 1), is a protein that in humans is encoded by the CNTN2 gene. This cell adhesion molecule plays a crucial role in the development of the nervous system, particularly in the formation of neural circuits and the process of myelination. Contactin 2 is a member of the immunoglobulin superfamily and is involved in the modulation of neuronal signaling and axon guidance, which are essential for proper brain function and development.

Structure[edit | edit source]

Contactin 2 is a glycosylphosphatidylinositol (GPI)-anchored protein, meaning it is attached to the cell membrane via a GPI anchor. This attachment method is significant for its role in cell-cell communication within the nervous system. The protein consists of multiple immunoglobulin-like domains and fibronectin type III domains, which are typical for molecules involved in cellular adhesion and signaling.

Function[edit | edit source]

The primary function of Contactin 2 is in the nervous system, where it plays a pivotal role in axon growth, guidance, and the formation of neural networks. It is involved in the process of myelination, the development of the myelin sheath around nerve fibers, which is crucial for the rapid transmission of nerve impulses. Contactin 2 interacts with various other proteins and receptors on the surfaces of neurons and glial cells, facilitating cell communication and signaling pathways that are essential for neural development and function.

Clinical Significance[edit | edit source]

Alterations in the expression or function of Contactin 2 have been associated with several neurological disorders. Mutations in the CNTN2 gene have been linked to conditions such as autism spectrum disorders (ASD) and other neurodevelopmental disorders. The protein's role in axon guidance and neural circuit formation suggests that disruptions in Contactin 2 signaling pathways could contribute to the pathophysiology of these conditions.

Additionally, Contactin 2 has been studied in the context of demyelinating diseases, such as multiple sclerosis (MS). Given its role in myelination, changes in Contactin 2 expression or function may influence the progression of demyelinating diseases by affecting the integrity of the myelin sheath and neural communication.

Research Directions[edit | edit source]

Ongoing research aims to further elucidate the molecular mechanisms by which Contactin 2 influences neural development and function. Understanding the complex interactions between Contactin 2 and other molecules within the nervous system could provide insights into the pathogenesis of neurological disorders and lead to the development of novel therapeutic strategies.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD