Target type: biologicalprocess
A process that is carried out at the cellular level that results in the assembly, arrangement of constituent parts, or disassembly of the T-tubule. A T-tubule is an invagination of the plasma membrane of a muscle cell that extends inward from the cell surface around each myofibril. [GOC:dph, GOC:jl, GOC:mah]
T-tubule organization is a complex and tightly regulated process crucial for efficient excitation-contraction coupling in muscle cells. It involves the formation of a network of invaginations of the sarcolemma, the plasma membrane of muscle cells, which penetrate deep into the muscle fiber. These invaginations, known as T-tubules, run alongside the sarcoplasmic reticulum (SR), an intracellular organelle responsible for calcium storage and release. The close proximity of T-tubules and SR allows for rapid and efficient transmission of action potentials from the sarcolemma to the SR, triggering calcium release and initiating muscle contraction.
The formation of T-tubules begins during muscle development, and their organization is influenced by a number of factors, including:
* **Genetic factors:** Genes encoding proteins involved in cytoskeleton formation, membrane trafficking, and calcium signaling play crucial roles in T-tubule organization. Mutations in these genes can lead to defects in T-tubule formation and function.
* **Mechanical forces:** Muscle contraction and stretching can influence T-tubule organization. These forces can induce changes in the cytoskeleton and membrane tension, leading to T-tubule remodeling and adaptation.
* **Signaling pathways:** Several signaling pathways, such as those involving calcium, calcineurin, and PI3K, are involved in regulating T-tubule organization. These pathways can modulate the expression of proteins involved in T-tubule formation and maintenance.
The process of T-tubule organization can be broadly divided into several steps:
1. **Budding of T-tubules:** T-tubules originate as invaginations of the sarcolemma, initiated by the formation of small buds at the cell surface. These buds are formed through the coordinated action of proteins involved in membrane trafficking and cytoskeletal remodeling.
2. **Elongation and branching:** Once formed, T-tubules elongate and branch out, forming a complex network throughout the muscle fiber. This process is guided by the cytoskeleton, particularly the actin and microtubule networks, which provide structural support and directionality.
3. **Association with SR:** As T-tubules elongate, they align with the SR, forming close contacts known as "triads." These triads are essential for efficient calcium release and muscle contraction.
4. **Maturation and stabilization:** Once formed, T-tubules undergo maturation and stabilization, involving the recruitment of specialized proteins that maintain their structure and function.
T-tubule organization is a dynamic process that can be modulated by various factors throughout the lifespan of a muscle cell. Disruptions in T-tubule organization can lead to impaired muscle function and contribute to various muscle diseases. Understanding the molecular mechanisms underlying T-tubule organization is therefore crucial for developing therapies for these diseases.'
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Protein | Definition | Taxonomy |
---|---|---|
Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 | A sarcoplasmic/endoplasmic reticulum calcium ATPase 2 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P16615] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
2,5-di-tert-butylhydroquinone | 2,5-di-tert-butylbenzene-1,4-diol : A member of the class of hydroquinones that is benzene-1,4-diol substituted by tert-butyl groups at position 2 and 5. | hydroquinones | |
paxilline | paxilline : An indole diterpene alkaloid with formula C27H33NO4 isolated from Penicillium paxilli. It is a potent inhibitor of large conductance Ca2(+)- and voltage-activated K(+) (BK)-type channels. paxilline: structure given in first source; RN given refers to (2R-(2alpha,4bbeta,6aalpha,12bbeta,12calpha,14abeta))-isomer | diterpene alkaloid; enone; organic heterohexacyclic compound; terpenoid indole alkaloid; tertiary alcohol | anticonvulsant; Aspergillus metabolite; EC 3.6.3.8 (Ca(2+)-transporting ATPase) inhibitor; genotoxin; geroprotector; mycotoxin; Penicillium metabolite; potassium channel blocker |
curcumin | curcumin : A beta-diketone that is methane in which two of the hydrogens are substituted by feruloyl groups. A natural dyestuff found in the root of Curcuma longa. Curcumin: A yellow-orange dye obtained from tumeric, the powdered root of CURCUMA longa. It is used in the preparation of curcuma paper and the detection of boron. Curcumin appears to possess a spectrum of pharmacological properties, due primarily to its inhibitory effects on metabolic enzymes. | aromatic ether; beta-diketone; diarylheptanoid; enone; polyphenol | anti-inflammatory agent; antifungal agent; antineoplastic agent; biological pigment; contraceptive drug; dye; EC 1.1.1.205 (IMP dehydrogenase) inhibitor; EC 1.1.1.21 (aldehyde reductase) inhibitor; EC 1.1.1.25 (shikimate dehydrogenase) inhibitor; EC 1.6.5.2 [NAD(P)H dehydrogenase (quinone)] inhibitor; EC 1.8.1.9 (thioredoxin reductase) inhibitor; EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor; EC 3.5.1.98 (histone deacetylase) inhibitor; flavouring agent; food colouring; geroprotector; hepatoprotective agent; immunomodulator; iron chelator; ligand; lipoxygenase inhibitor; metabolite; neuroprotective agent; nutraceutical; radical scavenger |
biselyngbyaside | biselyngbyaside: antineoplastic from the marine cyanobacterium Lyngbya sp.; structure in first source | ||
alpha-cyclopiazonic acid | alpha-cyclopiazonic acids |