Neurotrophin

From WikiMD's Wellness Encyclopedia

Revision as of 01:20, 20 February 2025 by Prab (talk | contribs) (CSV import)

Neurotrophin Signaling and p75NTR-JNK Mediated Apoptosis

File:Neurotrophin P75NTR-JNK-mediated Apoptosis.png
Diagram of p75NTR-JNK mediated apoptosis pathway

The neurotrophin receptor p75NTR is a member of the tumor necrosis factor receptor superfamily and plays a crucial role in the regulation of neuronal apoptosis. This receptor is known for its ability to bind to all neurotrophins, including nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophin-3 (NT-3), among others. The binding of neurotrophins to p75NTR can lead to various cellular outcomes, including cell survival, differentiation, or apoptosis, depending on the cellular context and the presence of co-receptors.

Structure of p75NTR

The p75 neurotrophin receptor (p75NTR) is a transmembrane protein characterized by an extracellular domain that binds neurotrophins, a single transmembrane domain, and a cytoplasmic domain that lacks intrinsic enzymatic activity. The cytoplasmic domain contains a "death domain," which is crucial for its role in apoptosis.

JNK Pathway Activation

Upon binding of neurotrophins, p75NTR can activate the c-Jun N-terminal kinase (JNK) signaling pathway. This activation is mediated through the recruitment of adaptor proteins such as NRIF (neurotrophin receptor interacting factor) and TRAF (TNF receptor-associated factor) proteins. The activation of JNK leads to the phosphorylation of c-Jun, a component of the activator protein 1 (AP-1) transcription factor complex, which can induce the expression of pro-apoptotic genes.

Mechanism of Apoptosis

The p75NTR-JNK pathway is implicated in the induction of apoptosis in neurons under certain conditions. When neurotrophins bind to p75NTR in the absence of Trk receptors, or when the balance of signaling favors p75NTR, the JNK pathway is activated, leading to apoptosis. This process involves the upregulation of pro-apoptotic proteins such as Bax and the downregulation of anti-apoptotic proteins like Bcl-2. The mitochondrial pathway of apoptosis is then activated, resulting in the release of cytochrome c and the activation of caspases, which execute the apoptotic program.

Physiological and Pathological Roles

The p75NTR-JNK mediated apoptosis pathway plays a significant role in the development of the nervous system, where it helps to eliminate excess neurons and refine neural circuits. However, dysregulation of this pathway can contribute to neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS), where inappropriate activation of apoptosis leads to neuronal loss.

Related Pages

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Ad. Transform your life with W8MD's Budget GLP-1 injections from $75


W8MD weight loss doctors team
W8MD weight loss doctors team

W8MD offers a medical weight loss program to lose weight in Philadelphia. Our physician-supervised medical weight loss provides:

NYC weight loss doctor appointmentsNYC weight loss doctor appointments

Start your NYC weight loss journey today at our NYC medical weight loss and Philadelphia medical weight loss clinics.

Linkedin_Shiny_Icon Facebook_Shiny_Icon YouTube_icon_(2011-2013) Google plus


Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.