2013
DOI: 10.1016/j.cbi.2012.10.009
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Acetylcholinesterase and agrin: Different functions, similar expression patterns, multiple roles

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Cited by 7 publications
(8 citation statements)
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“…Because agrin is released into the muscle basal lamina, it might interact with other receptors or molecules, such as α-dystroglycan (Singhal & Martin, 2011), and recent studies have shown agrin affecting the maturation of the excitation-contraction (E-C) coupling apparatus (Bandi, Jevsek, Mars, et al, 2008) and membrane electrical properties by changing of Na + /K + ATPase and ion channel expression (Jurdana et al, 2009) in developing human skeletal muscle cells. Although the underlying mechanism of the transcriptional regulation of myogenic genes by agrin remains unclear, some studies have shown positive effects of agrin on myogenesis through the increased expression of myosin heavy chains in agrintreated myotubes (Ko et al, 2013;Mis et al, 2013). It has also been reported that agrin promotes contractile function (twitch and tetanus force generation) in bioengineered rodent muscle constructs (Bian & Bursac, 2012).…”
Section: Discussionmentioning
confidence: 99%
“…Because agrin is released into the muscle basal lamina, it might interact with other receptors or molecules, such as α-dystroglycan (Singhal & Martin, 2011), and recent studies have shown agrin affecting the maturation of the excitation-contraction (E-C) coupling apparatus (Bandi, Jevsek, Mars, et al, 2008) and membrane electrical properties by changing of Na + /K + ATPase and ion channel expression (Jurdana et al, 2009) in developing human skeletal muscle cells. Although the underlying mechanism of the transcriptional regulation of myogenic genes by agrin remains unclear, some studies have shown positive effects of agrin on myogenesis through the increased expression of myosin heavy chains in agrintreated myotubes (Ko et al, 2013;Mis et al, 2013). It has also been reported that agrin promotes contractile function (twitch and tetanus force generation) in bioengineered rodent muscle constructs (Bian & Bursac, 2012).…”
Section: Discussionmentioning
confidence: 99%
“…Catalytic AChE subunits synthetized in motor neurons have different functions and must therefore be targeted to different places: targeting is obviously determined by its binding to appropriate structural subunit. Similar temporal patterns of expression of ColQ and synaptogenetic variant of agrin in motor neurons supports the possibility that tailed AChE is delivered to the same target, i.e., basal lamina in the synaptic cleft, as agrin [ 8 ].…”
Section: The Expression Of Ache During Nmj Formation In Co-culturementioning
confidence: 68%
“…Expression pattern of AChE and synaptogenetic (z8 and z19) and non-synaptogenetic (z0) agrin isoforms (for nomenclature see subchapter 4 below) in the spinal cord provides additional, albeit indirect, support for the notion that motor neurons contribute to the basal lamina-bound AChE [ 8 ]. As assessed by in situ hybridization and PCR, expression of the synaptogenetic agrin-z8 isoform and ColQ, which enables AChE binding to basal lamina of NMJ, increase in parallel after NMJ basal lamina is formed.…”
Section: The Expression Of Ache During Nmj Formation In Co-culturementioning
confidence: 99%
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“…Newly formed (i.e., recovering) NMJs have been shown to have the capacity for endplate potentials; however, contraction of myofibers is not achieved [ 28 ], that is, the NMJ did not perform its original function, despite the completion of nerve regeneration and sufficient contact between myofibers and neurons. Moreover, original reconstructed NMJ has been shown to exhibit incomplete function, and the reconstruction of NMJ function (i.e., the impulse) still requires the auxiliary function of nerve and muscle signaling molecules [ 29 - 32 ].…”
Section: Discussionmentioning
confidence: 99%