Synaptopodin is a cytoskeletal protein that plays a critical role in the structure and function of dendritic spines, which are essential for synaptic transmission and plasticity. It is involved in the organization of the actin cytoskeleton within these spines, contributing to their shape, size, and strength. This function is crucial for the maintenance of synaptic connections and the modulation of synaptic strength, which are vital for learning and memory. Synaptopodin interacts with various signaling pathways to regulate cytoskeletal dynamics and synaptic function, making it a key player in the neuronal response to different physiological stimuli.
The activation of Synaptopodin involves intricate signaling mechanisms that enhance its role in cytoskeletal and synaptic regulation. Direct activators of Synaptopodin have not been explicitly identified; however, indirect activation occurs through various signaling pathways that influence cytoskeletal dynamics, including the cAMP/PKA pathway, PKC, MAPK pathways, and the Wnt signaling pathway. These pathways can alter the phosphorylation state of proteins involved in the regulation of the actin cytoskeleton, promoting cytoskeletal rearrangements that support synaptic structure and function. Furthermore, the modulation of cyclic nucleotide levels by phosphodiesterase inhibitors provides a means to indirectly influence Synaptopodin's activity by altering the signaling environment within the cell, thereby impacting cytoskeletal organization and synaptic plasticity. Through these mechanisms, the functional activation of Synaptopodin is achieved, contributing to the stabilization of dendritic spines and the facilitation of synaptic transmission, which are essential for cognitive functions.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin activates adenylate cyclase, increasing cyclic AMP (cAMP) levels in cells. Elevated cAMP promotes protein kinase A (PKA) activity, which can phosphorylate various proteins, including those involved in cytoskeletal rearrangements. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA is a potent activator of protein kinase C (PKC). PKC activation can lead to the phosphorylation of substrates that regulate the actin cytoskeleton and synaptic plasticity. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
Isoproterenol, a beta-adrenergic agonist, stimulates the beta-adrenergic receptors, leading to adenylate cyclase activation and increased cAMP levels. The subsequent activation of PKA can phosphorylate proteins that modulate the actin cytoskeleton. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $75.00 $212.00 | 18 | |
Rolipram inhibits phosphodiesterase 4 (PDE4), preventing cAMP breakdown. Elevated cAMP levels activate PKA, which influences various signaling pathways including those affecting the cytoskeleton and synaptic function. | ||||||
Cilostazol | 73963-72-1 | sc-201182 sc-201182A | 10 mg 50 mg | $107.00 $316.00 | 3 | |
Cilostazol inhibits phosphodiesterase 3 (PDE3), resulting in increased cAMP levels, which activate PKA. PKA plays a critical role in modulating the cytoskeleton and synaptic function. | ||||||
Anisomycin | 22862-76-6 | sc-3524 sc-3524A | 5 mg 50 mg | $97.00 $254.00 | 36 | |
Anisomycin is a protein synthesis inhibitor that, paradoxically, activates stress-activated protein kinases (SAPKs) and p38 MAPK, pathways involved in neuronal plasticity and cytoskeletal reorganization. | ||||||
Lithium Chloride | 7447-41-8 | sc-203110 sc-203110A sc-203110B sc-203110C sc-203110D sc-203110E | 50 g 250 g 1 kg 2.5 kg 5 kg 10 kg | $32.00 $62.00 $173.00 $347.00 $614.00 $1163.00 | 8 | |
Lithium chloride activates the Wnt signaling pathway, which is involved in the regulation of synaptic plasticity and cytoskeletal architecture. |