- Research article
- Open Access
- Open Peer Review
Sodium nitrate decreases agrin-induced acetylcholine receptor clustering
© Jarosz et al. 2016
- Received: 18 November 2015
- Accepted: 14 April 2016
- Published: 1 May 2016
Humans are exposed to nitrate predominantly through diet with peak plasma concentrations within an hour after ingestion, but additional exposure is obtained from the environment, and minimally through de novo synthesis. Higher nitrate consumption has been associated with methemoglobinemia, spontaneous abortions, atherosclerosis, myocardial ischemia, septic and distressed lung, inflammatory bowel disease, amyotrophic lateral sclerosis, and neural tube defects. However, skeletal muscle development has not been examined.
C2C12 skeletal muscle cell cultures were maintained, myoblasts were fused into myotubes, and then cultures were exposed to motor neuron derived agrin to enhance acetylcholine receptor (AChR) clustering. Untreated cultures were compared with cultures exposed to sodium nitrate at concentrations ranging from 10 ng/mL–100 μg/mL.
The results reported here demonstrate that 1 μg/mL sodium nitrate was sufficient to decrease the frequency of agrin-induced AChR clustering without affecting myotube formation. In addition, concentrations of sodium nitrate of 1 μg/mL or 100 μg/mL decreased gene expression of the myogenic transcription factor myogenin and AChR in correlation with the agrin-induced AChR clustering data.
These results reveal that sodium nitrate decreases the frequency of agrin-induced AChR clustering by a mechanism that includes myogenin and AChR gene expression. As a consequence sodium nitrate may pose a risk for skeletal muscle development and subsequent neuromuscular synapse formation in humans.
- Sodium nitrate
For over 70 years methemoglobinemia in infants has been linked to nitrate consumption [1, 2]. Normally a small percentage of hemoglobin exists as methemoglobin (about 1–2 %), which is due to genetic factors or chemical exposure and typically does not result in health issues. When that percentage increases, methemoglobinemia may result, decreasing the oxygen carrying capacity and distribution by the affected hemoglobin. Nitrate reduced to nitrite will oxidize ferrous iron causing a shift to methemoglobin which has been linked to methemoglobinemia in infants whose formula was made with well water . Not all infants developed methemoglobinemia and so it is believed that the involvement of nitrate or nitrite is a cofactor in this disease .
Correlations between nitrate intake and gestational complications such as increased spontaneous abortions have been noted . Studies in animals have shown that nitrate, nitrite and N-nitroso compounds are all capable of crossing the placenta [4–6], and there have been cases of abortions in pigs pastured or housed in feedlots with oats and rape containing high levels of nitrates, 0.53 % and 5.52 % respectively . Studies have considered whether or not nitrate is involved in spontaneous abortions in humans [3, 8]. A study in Bulgaria found that women with high nitrate exposure suffered from one or more complications, with 67 % having anemia, 23 % toxemia, and 33 % spontaneous abortions or premature delivery. Of the population studied only 16 % had a normal pregnancy .
Gastric generation of nitrotyrosines from increased nitrite intake have been detectable in vivo and have been found in tissues associated with multiple pathologies: atherosclerosis, myocardial ischemia, septic and distressed lung, inflammatory bowel disease, and amyotrophic lateral sclerosis [10, 11]. In addition, higher rates of neural tube defects have been reported for fetuses of pregnant women who took nitrosatable drugs or drank water with higher levels of nitrate .
Humans are exposed to nitrate predominantly through diet with peak plasma concentrations 60 min after ingestion . Some nitrate exposure is obtained from the environment, and additionally (though minimally) through de novo synthesis. In the diet consumption is primarily from fruits and vegetables, which comprise 60–80 % of the nitrate ingested . A secondary source of dietary consumption is cured meats. Sodium nitrate and its reduced form sodium nitrite are used by the meat industry to prevent microbial growth (namely c. botulinum) and retain the color of preserved and cured meats . Dietary intake is estimated at 50–140 mg/day in Europe and 40–100 mg/day in the United States .
De novo synthesis of nitrate has been estimated to range from 500 to 1000 μmol/day [16, 17]. In a study where human subjects consumed a diet with slightly less than average nitrate levels, endogenous nitrate was reported at an average of 870 μmol/day . The higher estimate of 1000 μmol/day translates into 62 mg/day, and when combined with estimates of dietary intake , the total nitrate exposure could be as high as 200 mg/day in Europe and 160 mg/day in the United States. Another study using 15NO3 − determined that endogenous nitrate production occurred at all levels of ingestion, however at higher levels of intake endogenous production was masked . The level of nitrate intake per day varies depending on age, gender, race/ethnicity, BMI and level of education .
Skeletal muscle development in fetuses of pregnant women exposed to high nitrate levels has not been examined. During skeletal muscle development, myoblasts proliferate and fuse to form multinucleated myotubes. Acetylcholine receptors (AChR) will cluster spontaneously but aggregation increases upon exposure to motor neuron derived agrin [20–22], as AChRs become part of the postsynaptic component of the neuromuscular synapse. In addition, the myogenic regulatory factor myogenin activates genes for AChR subunits [23, 24], suggesting that myogenic regulatory factors like myogenin are intricately linked to the development of the postsynaptic component. Exposure to nicotine, caffeine, ethanol, and mercury have been demonstrated to decrease AChR clustering in C2C12 myotubes [25–28], whereas methoxychlor has been demonstrated to decrease myotube formation by slowing myoblast proliferation without affecting AChR clustering .
The objective of the current study was to investigate whether sodium nitrate affects skeletal muscle development, specifically the events of myoblast fusion into myotubes and AChR clustering. And if there is an effect, does sodium nitrate mediate that effect by interfering with myogenin or AChR expression. Skeletal muscle cell cultures, such as the C2C12 cell line derived from mouse hindlimb, provide simplified systems for studying development of the postsynaptic component of the neuromuscular synapse [30, 31]. The C2C12 cell culture model has proven useful for asking fundamental questions concerned with muscle development and neuromuscular synapse formation, and is ideal for examining how sodium nitrate might interfere with these developmental events. The results reported here demonstrate that 1 μg/mL sodium nitrate was sufficient to decrease the frequency of agrin-induced AChR clustering without affecting myotube formation. In addition, sodium nitrate decreased myogenin and AChR gene expression in correlation with the agrin-induced AChR clustering data.
Cell culture maintenance
C2C12 myoblasts were derived from mouse hind limb (gift from H. Gordon, University of Arizona) [30, 31], and are commonly used for skeletal muscle cell culture experiments. They are ideal for studying myoblast fusion to form myotubes, and acetylcholine receptor (AChR) clustering. For normal maintenance of C2C12 cell culture, myoblasts were first plated in growth medium (GM) on 10 cm plates at approximately 20 % confluence. GM consists of Dulbecco’s modified Eagle’s medium (DMEM) plus 20 % fetal bovine serum, 0.5 % chick embryo extract and 100 U/mL penicillin. Fresh GM was added daily, and myoblast cultures were split into new plates at approximately 60 % confluence. For formation of myotubes, myoblasts were plated in GM on 22×22 mm cover slips that had been flamed in 200-proof ethanol and placed in 6-well plates. Fresh GM was added daily. After 48 h in GM, myoblast cultures typically reached 90 % confluence, and cultures were then switched to differentiation medium (DM). DM consists of DMEM plus 2 % horse serum and 100 U/mL penicillin. Fresh DM was added daily as myoblasts fused to form myotubes, and cultures were maintained for 72 h in DM. All cultures were exposed to 10 ng/mL agrin (R&D Systems) for the last 16 h of 72 h in DM to induce AChR clustering. Some cultures were exposed to 10 ng/mL–100 μg/mL sodium nitrate (NaNO3; Sigma-Aldrich) for the last 48 h of 72 h in DM. A 1 g/mL NaNO3 stock solution was prepared in DM and then serial dilutions were performed to achieve the treatment concentrations. It would be difficult to correlate nitrate dietary intake and endogenous nitrate production with nitrate treatment in cell culture. At best cell culture might mirror fetal exposure to toxins in maternal blood to some degree. Therefore, a range of NaNO3 concentrations were tested in cell culture to investigate any effect on AChR clustering, myotube formation, and myogenin and AChR gene expression.
Acetylcholine receptor clustering assay
AChRs were labeled by the binding of α-bungarotoxin conjugated to tetramethyl rhodamine (Molecular Probes) . Cultures were incubated in the toxin-containing medium for 30 min at 37 °C to label AChRs after 72 h in DM. The cover slips were rinsed three times with room temperature phosphate buffered saline (PBS), fixed for 10 min with 2 % paraformaldehyde in PBS, rinsed three times with PBS, dehydrated in cold methanol for 5 min at −20 °C, and mounted on microscope slides in Vectashield Mounting Medium for Fluorescence (Vector Laboratories). For some experiments the mounting medium contained 4’6-diamidino-2-phenylindole (DAPI) to visualize nuclei. AChR clusters were visualized with an IX70 Olympus inverted microscope under the 20X objective (yielding a total magnification of 200X), and fluorescent images were captured as high-resolution JPG files with an Olympus camera with Magnafire digital imaging software. Bright clusters of AChRs were observed on all aspects of myotubes in fluorescent images. AChR clusters were counted from 25 images captured from each cover slip using ImageJ software. One cover slip was analyzed for each treatment group in each replicate experiment. These data were utilized to assay agrin-induced AChR clustering in untreated cultures, or after exposure to 10 ng/mL–100 μg/mL NaNO3 for the last 48 h of 72 h in DM. Comparisons of untreated cultures with cultures exposed to NaNO3 were analyzed by Student’s t-test to determine statistically different results at p < 0.05. Representative images were assembled into Fig. 2.
Myotube formation index
Myotube formation index
Nuclei in myotubes
Nuclei in myoblasts
Fraction of nuclei in myotubes
Untreated (n = 6)
1 μg/ml NaNO3 (n = 5)
10 μg/ml NaNO3 (n = 5)
Comparison of NaNO3 effects
Myogenin expression signal
Actin expression signal
Percent compared with untreated
1 μg/ml NaNO3
100 μg/ml NaNO3
AChR expression signal
Actin expression signal
Percent compared with untreated
1 μg/ml NaNO3
100 μg/ml NaNO3
Agrin-induced AChR clustering
AChR clusters per field of view
Percent compared with untreated
1 μg/ml NaNO3
100 μg/ml NaNO3
NaNO3 decreases the frequency of agrin-induced AChR clusters
NaNO3 has no effect on myotube formation
NaNO3 decreases myogenin and AChR gene expression
The results reported here demonstrate that sodium nitrate decreases the frequency of agrin-induced acetylcholine receptor (AChR) clustering in correlation with a decrease in myogenin and AChR gene expression. This suggests that sodium nitrate may interfere with normal developmental events by initially decreasing myogenin gene expression, which causes a decrease in AChR gene expression, and ultimately results in fewer AChRs available to cluster in response to agrin stimulation.
Myogenin is one of several myogenic transcription factors that guide skeletal muscle development. Myogenin directly activates rapsyn gene expression  and the genes for AChR subunits [23, 24]. Rapsyn is one of several postsynaptic molecules that is essential for the formation of AChR clusters during neuromuscular synapse formation . Another is a muscle specific kinase (MuSK) that is essential for the signaling events that precede AChR clustering [36–39]. These signaling events are initiated when motor neuron derived agrin binds to low-density lipoprotein receptor-related protein (Lrp4) [40, 41] to stimulate tyrosine phosphorylation of MuSK  and the subsequent signaling pathway that includes the tyrosine phosphorylation of the AChR β subunit leading to increased AChR clustering [42, 43]. Suppression of Lrp4 gene expression decreases agrin binding activity, agrin-induced MuSK tyrosine phosphorylation, and agrin-induced AChR clustering .
In the data reported in Table 2, when compared with untreated cell cultures, treatment with 1 μg/ml sodium nitrate decreased myogenin gene expression to 89 % of the untreated level, and treatment with 100 μg/ml sodium nitrate decreased myogenin gene expression to 54 % of the untreated level. This correlated with a consequent decrease in AChR gene expression to 60 % of the untreated level with 1 μg/ml sodium nitrate treatment, and a decrease to 36 % of the untreated level with 100 μg/ml sodium nitrate treatment. Decreases in myogenin and AChR gene expression also correlated with decreased agrin-induced AChR clustering, where treatment with 1 μg/ml sodium nitrate decreased agrin-induced AChR clustering to 48 % of the untreated level, and treatment with 100 μg/ml sodium nitrate decreased agrin-induced AChR clustering to 39 % of the untreated level. This data shows that the level of agrin-induced AChR clustering is directly correlated with the level of AChR gene expression, supporting the interpretation that with sodium nitrate treatment fewer AChRs are available to cluster in response to agrin stimulation. Finally, with sodium nitrate treatment of 0.01 μg/ml agrin-induced AChR clustering and myogenin gene expression were unaffected, while AChR gene expression was decreased to 66 % of the untreated level (data not shown), suggesting AChR gene expression is more sensitive to sodium nitrate levels than myogenin gene expression and that AChR gene expression is not the sole determinant of agrin-induced AChR clustering.
Myogenin was previously shown to be essential for myoblast differentiation [44, 45]. In the data reported here, concentrations of sodium nitrate as high as 10 μg/ml had no effect on myotube formation. The fraction of nuclei in myotubes was 0.8922 for untreated cultures, 0.8803 for cultures treated with 1 μg/ml sodium nitrate, and 0.8623 for cultures treated with 10 μg/ml sodium nitrate. In contrast, concentrations as low as 1 μg/ml were sufficient to decrease agrin-induced AChR clustering. This may reflect a difference in sensitivity to myogenin levels between myotube formation and agrin-induced AChR clustering. Alternately, this may reflect the time sequence, since myotube formation occurs prior to synapse formation and AChR clustering in normal skeletal muscle development. A previous study showed that treatment of C2C12 cells with myogenin antibodies also decreased agrin-induced AChR clustering without affecting myotube formation .
The reduction in AChR clustering caused by sodium nitrate could have a functional outcome similar to common neuromuscular disorders. As an example, patients with the autoimmune disease myasthenia gravis have muscle weakness due to a decrease in functional AChRs. In contrast, patients with muscular dystrophy have muscle weakness due to neuromuscular synapses that have reduced or absent postsynaptic molecules other than AChRs. However the functional outcome is the same, muscle weakness. The data reported here suggests that any disease process that affects myogenin gene expression could also lead to muscle weakness due to a decrease in AChR clustering at neuromuscular synapses caused by a decrease in AChR gene expression. For further inquiry it might be useful to replicate these experiments using other cell lines including human muscle cell lines to see if the results are universal across species.
The results reported here demonstrate that 1 μg/mL sodium nitrate was sufficient to decrease the frequency of agrin-induced AChR clustering without affecting myotube formation. In addition, sodium nitrate decreased myogenin and AChR gene expression in correlation with the agrin-induced AChR clustering data. These results demonstrate that sodium nitrate decreases the frequency of agrin-induced AChR clustering by a mechanism that includes myogenin and AChR gene expression. As a consequence sodium nitrate may pose a risk for skeletal muscle development and subsequent neuromuscular synapse formation in humans.
This work was supported by Midwestern University funding through the Biomedical Sciences Program (Jess Jarosz) and the Office of Research and Sponsored Programs (Cullen White and Wade A. Grow). In addition, Senior Research Associate Kelly Ezell provided technical expertise. A preliminary account of this work has appeared in abstract form .
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Comly HH. Cyanosis in infants caused by nitrates in well water. JAMA. 1945;129:112–6.View ArticleGoogle Scholar
- Fewtrell L. Drinking-water nitrate, methemoglobinemia, and global burden of disease: A discussion. Environ Health Perspect. 2004;112:1371–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Schmitz JT. Methemoglobinemia – a cause of abortions? A preliminary report. Obstet Gynecol. 1961;17:413–5.PubMedGoogle Scholar
- Gruener N, Shuval HI, Behroozi K, Cohen S, Shechter H. Methemoglobinemia induced by transplantal passage of nitrate in rats. Bull Environ Contam Toxicol. 1973;9:44–8.View ArticlePubMedGoogle Scholar
- Fan AM, Willhite CC, Book SA. Evaluation of the nitrate drinking water standard with reference to infant methemoglobinemia and potential reproductive toxicity. Regul Toxicol Pharmacol. 1987;7:135–48.View ArticlePubMedGoogle Scholar
- Brunning-Fan CS, Kaneene JB. The effects of nitrate, nitrite and N-nitroso compounds on human health: A review. Vet Hum Toxicol. 1993;35:521–38.Google Scholar
- Case AA. Abortion in swine due to excess nitrate. Journal of the American Veterinary Medical Association. 1957;131–226.Google Scholar
- Skrivan J. Methemoglobinemia in pregnancy (clinical and experimental study). Acta Universitatis Carolinea Medica (Praha). 1971;17:123–61.Google Scholar
- Tabacova S, Balabaeva L, Little RE. Maternal exposure to exogenous nitrogen compounds and complications of pregnancy. Arch Environ Health. 1997;52:341–7.View ArticlePubMedGoogle Scholar
- Archer MC. Mechanisms of action of N-nitroso compounds. Cancer Survivor. 1989;8:241–50.Google Scholar
- Beckman JS, Koppenol WH. Nitric oxide, superoxide, and peroxynitrite: The good, the bad, and ugly. Am J Cell Physiol. 1996;271:C1424–37.Google Scholar
- Brender JD, Olive JM, Felkner M, Suarez L, Marckwardt W, Hendricks KA. Dietary nitrites and nitrates, nitrosatable drugs, and neural tube defects. Epidemiology. 2004;15:330–6.View ArticlePubMedGoogle Scholar
- McKnight GM, Smith LM, Drummond RS, Duncan CW, Golden M, Benjamin N. Chemical synthesis of nitric oxide in the stomach from dietary nitrate in humans. Gut. 1997;40:211–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Ysart G, Miller P, Barrett G, Farrington D, Lawrence P, Harrison N. Dietary exposures to nitrate in the UK. Food Addit Contam. 1999;16:521–32.View ArticlePubMedGoogle Scholar
- Mensinga TT, Speijers GJ, Meulenbelt J. Health implications of exposure to environmental nitrogenous compounds. Toxicol Rev. 2003;22:41–51.View ArticlePubMedGoogle Scholar
- Green LC, De Luzuriaga KR, Wagner DA, Rand W, Istfan N, Young VR, Tanenbaum SR. Nitrate biosynthesis in man. Proc Natl Acad Sci. 1981;78:7764–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Tanenbaum SR, Fett D, Young VR, Land PD, Bruce WR. Nitrite and nitrate are formed by endogenous synthesis in the human intestine. Science. 1978;200:1487–9.View ArticleGoogle Scholar
- Lee K, Greger JL, Consaul JR, Graham KL, Chinn BL. Nitrate, nitrite balance, and de novo synthesis of nitrate in humans consuming cured meats. Am J Clin Nutr. 1986;44:188–94.PubMedGoogle Scholar
- Griesenbeck JS, Brender JD, Sharkey JR, Steck MD, Huber JC, Rene AA, McDonald TJ, Romitti PA, Canfield MA, Langlois PH, Suarez L. Maternal characteristics associated with the dietary intake of nitrates, nitrites, and nitrosamines in women of child-bearing age: a cross-sectional study. Environ Health. 2010;9:10.View ArticlePubMedPubMed CentralGoogle Scholar
- Godfrey EW, Nitkin RM, Wallace BG, Rubin LL, McMahan UJ. Components of Torpedo electric organ and muscle that cause aggregation of acetylcholine receptors on cultured muscle cells. J Cell Biol. 1984;99:615–27.View ArticlePubMedGoogle Scholar
- Nitkin RM, Smith MA, Magill C, Fallon JR, Yao YM, Wallace BG, McMahan UJ. Identification of agrin, a synaptic organizing protein from Torpedo electric organ. J Cell Biol. 1987;105:2471–8.View ArticlePubMedGoogle Scholar
- McMahan UJ. The agrin hypothesis. Cold Spring Harb Symp Quant Biol. 1990;55:407–18.View ArticlePubMedGoogle Scholar
- Tang H, Sun Z, Goldman D. CaM kinase II-dependent suppression of nicotinic acetylcholine receptor delta-subunit promoter activity. J Biol Chem. 2001;276:26057–65.View ArticlePubMedGoogle Scholar
- Tang H, Macpherson P, Argetsinger LS, Cieslak D, Suhr ST, Carter-Su C, Goldman D. CaM kinase II-dependent phosphorylation of myogenin contributes to activity-dependent suppression of nAChR gene expression in developing rat myotubes. Cell Signal. 2004;16:551–63.View ArticlePubMedGoogle Scholar
- Ferayorni AJ, Gunville CF, Grow WA. Nicotine decreases agrin signaling and acetylcholine receptor clustering in C2C12 myotube culture. J Neurobiol. 2004;60:51–60.View ArticlePubMedGoogle Scholar
- Miller TJ, Grow WA. Mercury decreases the frequency of induced but not spontaneous clustering of acetylcholine receptors. Cell Tissue Res. 2004;316:211–9.View ArticlePubMedGoogle Scholar
- Kordosky-Herrera K, Grow WA. Caffeine and nicotine decrease acetylcholine receptor clustering in C2C12 myotube culture. Cell Tissue Res. 2009;335:341–8.View ArticlePubMedGoogle Scholar
- Owen DB, Chamberlain KT, Shishido S, Grow WA. Ethanol decreases agrin-induced acetylcholine receptor clustering in C2C12 myotube culture. Toxicol in Vitro. 2010;24:645–51.View ArticlePubMedGoogle Scholar
- Steffens BW, Batia LM, Baarson CJ, Choi CKC, Grow WA. The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation. Toxicol in Vitro. 2007;21:770–81.View ArticlePubMedGoogle Scholar
- Yaffe D, Saxel O. Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle. Nature. 1977;270:725–7.View ArticlePubMedGoogle Scholar
- Blau HM, Pavlath GK, Hardeman EC, Chiu CP, Silberstein L, Webster SG, Miller SC, Webster C. Plasticity of the differentiated state. Science. 1985;230:758–66.View ArticlePubMedGoogle Scholar
- Ravdin P, Axelrod D. Fluorescent tetramethyl rhodamine derivatives of alpha-bungarotoxin: preparation, separation, and characterization. Anal Biochem. 1977;80:585–92.View ArticlePubMedGoogle Scholar
- Rando TA, Blau HM. Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy. J Cell Biol. 1994;125:1275–87.View ArticlePubMedGoogle Scholar
- Blais A, Tsikitis M, Acosta-Alvear D, Sharan R, Kluger T, Dynlacht BD. An initial blueprint for myogenic differentiation. Genes Dev. 2005;19:553–69.View ArticlePubMedPubMed CentralGoogle Scholar
- Gautam M, Noakes PG, Mudd J, Nichol M, Chu GC, Sanes JR, Merlie JP. Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice. Nature. 1995;377:232–6.View ArticlePubMedGoogle Scholar
- Bowen DC, Park JS, Bodine S, Stark JL, Valenzuela DM, Stitt TN, Yancopoulos GD, Lindsay RM, Glass DJ, DiStefano PS. Localization and regulation of MuSK at the neuromuscular junction. Dev Biol. 1998;199:309–19.View ArticlePubMedGoogle Scholar
- Gautam M, DeChiara TM, Glass DJ, Yancopoulos GD, Sanes JR. Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn. Brain Res Dev Brain Res. 1999;114:171–8.View ArticlePubMedGoogle Scholar
- Glass DJ, Bowen DC, Stitt TN, Radziejewski C, Bruno J, Ryan TE, Gies DR, Shah S, Mattsson K, Burden SJ, DeStefano PS, Valenzuela DM, DeChiara TM, Yancopolous GD. Agrin acts via a MuSK receptor complex. Cell. 1996;85:513–23.View ArticlePubMedGoogle Scholar
- Sugiyama JE, Glass DJ, Yancopoulos GD, Hall ZW. Laminin-induced acetylcholine receptor clustering: an alternative pathway. J Cell Biol. 1997;139:181–91.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim N, Stiegler AL, Cameron TO, Hallock PT, Gomez AM, Huang JH, Hubbard SR, Dustin ML, Burden SJ. Lrp4 is a receptor for agrin and forms a complex with MuSK. Cell. 2008;135:334–42.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang B, Luo S, Wang Q, Suzuki T, Xiong WC, Mei L. Lrp4 serves as a co-receptor of agrin. Neuron. 2008;60:285–97.View ArticlePubMedPubMed CentralGoogle Scholar
- Ferns M, Deiner M, Hall Z. Agrin-induced acetylcholine receptor clustering in mammalian muscle requires tyrosine phosphorylation. J Cell Biol. 1996;132:937–44.View ArticlePubMedGoogle Scholar
- Wallace BG, Qu Z, Huganir RL. Agrin induces phosphorylation of the nicotinic acetylcholine receptor. Neuron. 1991;6:869–78.View ArticlePubMedGoogle Scholar
- Hasty P, Bradley A, Morris JH, Edmondson DG, Venuti JM, Olson EN, Klein WH. Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene. Nature. 1993;364:501–6.View ArticlePubMedGoogle Scholar
- Nabeshima Y, Hanaoka K, Hayasaka M, Esumi E, Li S, Nonaka I, Nabeshima Y. Myogenin gene disruption results in perinatal lethality because of severe muscle defect. Nature. 1993;364:532–5.View ArticlePubMedGoogle Scholar
- Ball MK, Campbell DH, Ezell K, Henley JB, Standley PR, Grow WA. Antibody to MyoD or myogenin decreases acetylcholine receptor clustering in C2C12 myotube culture. Cell Bio. 2013;2:138–48.Google Scholar
- White C, Grow W. Sodium nitrate decreases agrin-induced AChR clustering. FASEB J. 2015;29:874.1.Google Scholar