Expression of plasma membrane Ca²(+)-ATPase isoform 2 in spiral ganglion cells of newborn rats.
- Author:
Qing-guo CHEN
1
;
Han-qi CHU
;
Xian-hong WANG
;
Jin CHEN
;
Jian-ling LI
;
Yong-hua CUI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Female; Male; Plasma Membrane Calcium-Transporting ATPases; metabolism; Protein Isoforms; metabolism; RNA Splice Sites; Rats; Rats, Sprague-Dawley; Spiral Ganglion; cytology; metabolism
- From: Chinese Journal of Otorhinolaryngology Head and Neck Surgery 2010;45(2):128-132
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the expression of plasma membrane Ca(2+)-ATPase isoform 2 (PMCA2) in spiral ganglion cell (SGC) from inner ear of newborn rats and further check PMCA2 splice variants at site A and C.
METHODSSpiral ganglion tissues isolated from cochlea of newborn rats (P3-P4) were cultured and identified in vitro. The cochlea of newborn rats (P3-P4) were isolated and cut into frozen sections. The expression of PMCA2 was detected by immunofluorescence analyses. The SGC cultured in 4 wells of the 6-well culture plate were collected and the total RNA was extracted by Trizol and reverse transcribed to cDNA. The site A and C splice variants of PMCA2 were respectively checked by nested PCR and common PCR.
RESULTSThe SGC grew well with good refraction and showed positive immunoreactivity for neuronal marker NF-200. Strong green fluorescence could be seen in cytomembrane, cytoplasm and neuritis, as well showing SGC immunoreactivity for PMCA2 antibody. In the cochlear sections, the spiral ganglion tissues were strongly stained by PMCA2. PMCA2z was present at splice site A, but PMCA2b and PMCA2c were present at splice site C.
CONCLUSIONSGC from newborn rats strongly expresses PMCA2 and different splice variants are present at PMCA2 splice site A and C.