| Title : Dual effects of insect nAChR chaperone RIC-3 on hybrid receptor: Promoting assembly on endoplasmic reticulum but suppressing transport to plasma membrane on Xenopus oocytes - Bao_2018_Neurochem.Int_115_24 |
| Author(s) : Bao H , Xu X , Liu W , Yu N , Liu Z |
| Ref : Neurochem Int , 115 :24 , 2018 |
|
Abstract :
Resistance to inhibitors of cholinesterase (RIC) -3 promotes the maturation (folding and assembly) of neuronal nicotinic acetylcholine receptors (nAChRs) as a molecular chaperone. The modulation effects of RIC-3 on homomeric alpha7 nAChRs are always positive, but its effects on heteromeric subtypes are inconsistent among reports. In this study, five RIC-3 isoforms were identified from Locusta migratoria. Four isoforms showed obvious effects on hybrid receptor Localpha1/rbeta2 expressed in Xenopus oocytes. As a representative, the co-expression of RIC-3v4 exhibited the decreased agonist responses (Imax) on oocytes, lower specific [(3)H]epibatidine binding (Bmax) on plasma membrane protein (PMP), and reduced subunit levels in PMP, which showed that the mature Localpha1/rbeta2 on the plasma membrane was decreased by the co-expression of RIC-3. In contrast, the [(3)H]epibatidine binding and mature Localpha1/rbeta2 levels in the endoplasmic reticulum membrane protein (ERMP) were much increased when co-expressing with RIC-3v4. The [(3)H]epibatidine binding and mature Localpha1/rbeta2 levels in total membrane protein (TMP) gave the similar results as that in ERMP. Taking data together, the results showed that the co-expression of RIC-3 increased the mature Localpha1/rbeta2 receptor levels on ER of Xenopus oocytes, but these mature receptors were mostly kept on ER and suppressed to transport to plasma membrane. |
| PubMedSearch : Bao_2018_Neurochem.Int_115_24 |
| PubMedID: 29032010 |
Bao H, Xu X, Liu W, Yu N, Liu Z (2018)
Dual effects of insect nAChR chaperone RIC-3 on hybrid receptor: Promoting assembly on endoplasmic reticulum but suppressing transport to plasma membrane on Xenopus oocytes
Neurochem Int
115 :24
Bao H, Xu X, Liu W, Yu N, Liu Z (2018)
Neurochem Int
115 :24