Axonal Remodeling
Axonal Remodeling - Related Videos
02:54
Nucleosome Remodeling
0 Views •
2020
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure. Nucleosome remodeling complex Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
09:25
Laser Nanosurgery of Cerebellar Axons In Vivo
0 Views •
Cited by 7 •
2014
Two-photon imaging, coupled to laser nanodissection, are useful tools to study degenerative and regenerative processes in the central nervous system with subcellular resolution. This protocol shows how to label, image, and dissect single climbing fibers in the cerebellar cortex in vivo.
03:24
Two-Photon Laser Axotomy: A Method to Injure Axons in Zebrafish Embryos and Observe Axonal Recovery
0 Views •
2023
This video describes the method to injure axons in zebrafish embryos using two photon laser axotomy and observing axonal recovery from injury.
07:31
A Model of Cardiac Remodeling Through Constriction of the Abdominal Aorta in Rats
0 Views •
Cited by 26 •
2016
A rat model of abdominal aortic constriction that induces cardiac hypertrophy and remodeling is described. An efficient, highly-reproducible, and minimally-invasive method is used to provide a simple yet useful platform for research in myocardial hypertrophy and dysfunction.
10:14
Biochemical Assays for Analyzing Activities of ATP-dependent Chromatin Remodeling Enzymes
0 Views •
Cited by 4 •
2014
Here we describe biochemical assays that can be used to characterize ATP-dependent chromatin remodeling enzymes for their abilities to 1) catalyze ATP-dependent nucleosome sliding, 2) engage with nucleosome substrates, and 3) hydrolyze ATP in a nucleosome- or DNA-dependent manner.
FAQs
Cytoskeletal dynamics provide an internal mechanism for changing axon structure during growth, branching, guidance, and pruning. By reorganizing the axon's structural framework, neurons can alter the routes and connections available to target cells. This mechanism links cellular architecture with circuit adaptation during development, learning, and responses to neural damage.
Extracellular signals and neuronal activity regulate which axonal changes are supported or maintained. Their influence can affect growth, guidance, branching, pruning, and synaptic connectivity, allowing developing or active circuits to be refined. These regulatory inputs help connect conditions outside the axon and patterns of neural use with changes in circuit architecture.
These processes shape connectivity in complementary ways. Growth and guidance help axons reach appropriate targets, branching expands potential connections, and pruning removes selected extensions or contacts. Together, they refine neural circuits rather than simply increasing their size. Their coordinated action is especially relevant to developmental organization and the circuit changes associated with learning.
During development, remodeling helps establish and refine neural circuits, while during learning it contributes to adaptive changes in connectivity. After injury, the same capacity may support partial neural repair, but it can also produce maladaptive rewiring. The outcome therefore depends on how structural changes affect circuit organization and functional connections.
Researchers can focus on changes in axon growth, branching, guidance, pruning, and synaptic connectivity, while also considering cytoskeletal dynamics, extracellular signals, and neuronal activity. Examining these features together helps relate cellular changes to circuit architecture. This approach supports investigation of development, neural plasticity, neurodegenerative disease, and recovery after neural damage.
Axonal remodeling provides a framework for studying how neural connections change when nervous system function is disrupted. It may reveal processes associated with disease-related circuit alterations, partial repair after injury, or maladaptive rewiring that limits recovery. Understanding these outcomes can guide research into strategies intended to promote more functional neural repair.