THE NEURO-2A NEUROBLASTOMA CELL-LINE EXPRESSES [MET]-ENKEPHALIN AND VASOPRESSIN MESSENGER-RNA AND PEPTIDE

被引:9
作者
BAMBERGER, AM [1 ]
PU, LP [1 ]
COOL, DR [1 ]
LOH, YP [1 ]
机构
[1] NICHHD,DEV NEUROBIOL LAB,CELLULAR NEUROBIOL SECT,BETHESDA,MD 20892
关键词
NEURO-2A CELL; ENKEPHALIN; PROHORMONE CONVERTASE 2; VASOPRESSIN;
D O I
10.1016/0303-7207(95)03625-H
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mouse neuroblastoma Neuro-2a cells were examined for the expression of pro-enkephalin mRNA, protein, and Met-enkephalin ([Met]-Enk) peptide. Reverse transcriptase/polymerase chain reaction (RT/PCR) and in situ hybridization demonstrated the presence of pro-enkephalin mRNA in these cells. Immunocytochemistry using an antibody which recognizes pro-enkephalin and high pressure liquid chromatography (HPLC) followed by radioimmunoassay indicated that pro-enkephalin was synthesized in these cells and processed to yield the bioactive pentapeptide, [Met]-Enk. Furthermore, release studies showed that the [Met]-Enk was secreted from these cells with high K+ stimulation. Using double labeling, in situ hybridization combined with immunocytochemistry, we demonstrated that prohormone convertase 2 (PC2) mRNA is colocalized with pro-enkephalin in the same Neuro-2a cells, suggesting that this enzyme may be responsible for processing this precursor. We also showed the presence of vasopressin mRNA and arginine-vasopressin peptide in these cells using in situ hybridization and immunocytochemistry, respectively. Thus, the Neuro-2a cells are a multiple neuropeptide-producing cell line and an excellent model for studying the mechanisms involved in the synthesis, intracellular targeting and processing of endogenous pro-enkephalin and pro-vasopressin, as well as other transfected neuropeptide precursors.
引用
收藏
页码:155 / 163
页数:9
相关论文
共 20 条
[1]   RAPID INCREASES IN PEPTIDE PROCESSING ENZYME EXPRESSION IN HIPPOCAMPAL-NEURONS [J].
BHAT, RV ;
TAUSK, FA ;
BARABAN, JM ;
MAINS, RE ;
EIPPER, BA .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (04) :1315-1322
[2]  
BRESLIN MB, 1993, J BIOL CHEM, V268, P27084
[3]   A NEWLY FOUND ANGIOTENSIN-II RECEPTOR SUBTYPE MEDIATES CYCLIC-GMP FORMATION IN DIFFERENTIATED NEURO-2A CELLS [J].
CHAKI, S ;
INAGAMI, T .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1992, 225 (04) :355-356
[4]   IDENTIFICATION AND CHARACTERIZATION OF A NEW BINDING-SITE FOR ANGIOTENSIN-II IN MOUSE NEUROBLASTOMA NEURO-2A CELLS [J].
CHAKI, S ;
INAGAMI, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (01) :388-394
[5]   IDENTIFICATION OF A SORTING SIGNAL FOR THE REGULATED SECRETORY PATHWAY AT THE N-TERMINUS OF PROOPIOMELANOCORTIN [J].
COOL, DR ;
LOH, YP .
BIOCHIMIE, 1994, 76 (3-4) :265-270
[6]   IDENTIFICATION OF THE SORTING SIGNAL MOTIF WITHIN PROOPIOMELANOCORTIN FOR THE REGULATED SECRETORY PATHWAY [J].
COOL, DR ;
FENGER, M ;
SNELL, CR ;
LOH, YP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (15) :8723-8729
[7]   CHARACTERIZATION OF PROOPIOMELANOCORTIN PROCESSING IN HETEROLOGOUS NEURONAL CELLS THAT EXPRESS PC2 MESSENGER-RNA [J].
DAY, NC ;
LIN, H ;
UEDA, Y ;
MEADORWOODRUFF, JH ;
AKIL, H .
NEUROPEPTIDES, 1993, 24 (05) :253-262
[8]   ISOLATION OF 2 COMPLEMENTARY DEOXYRIBONUCLEIC-ACID CLONES FROM A RAT INSULINOMA CELL-LINE BASED ON SIMILARITIES TO KEX2 AND FURIN SEQUENCES AND THE SPECIFIC LOCALIZATION OF EACH TRANSCRIPT TO ENDOCRINE AND NEUROENDOCRINE TISSUES IN RATS [J].
HAKES, DJ ;
BIRCH, NP ;
MEZEY, A ;
DIXON, JE .
ENDOCRINOLOGY, 1991, 129 (06) :3053-3063
[9]   EXPRESSION OF PC2 AND PC1/PC3 IN HUMAN PHEOCHROMOCYTOMAS [J].
KONOSHITA, T ;
GASC, JM ;
VILLARD, E ;
TAKEDA, R ;
SEIDAH, NG ;
CORVOL, P ;
PINET, F .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 99 (02) :307-314
[10]   TARGETING AND PROCESSING OF PRO-OPIOMELANOCORTIN IN NEURONAL CELL-LINES [J].
NOEL, G ;
ZOLLINGER, L ;
LALIBERTE, F ;
RASSART, E ;
CRINE, P ;
BOILEAU, G .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (04) :1050-1057