IMMUNOCYTOCHEMICAL DETECTION OF PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE LOCALIZATION SITES WITHIN THE NUCLEUS

被引:84
作者
MAZZOTTI, G
ZINI, N
RIZZI, E
RIZZOLI, R
GALANZI, A
OGNIBENE, A
SANTI, S
MATTEUCCI, A
MARTELLI, AM
MARALDI, NM
机构
[1] IOR,CNR,INST CITOMORFOL NORMALE & PATOL,I-40136 BOLOGNA,ITALY
[2] UNIV BOLOGNA,INST ANAT UMANA NORMALE,BOLOGNA,ITALY
[3] IOR,INST RES CODIVILLA PUTTI,BIOL CELLULARE & MICROSCOPIA ELETTR LAB,BOLOGNA,ITALY
[4] UNIV TRIESTE,DEPT MORFOL UMANA NORMALE,TRIESTE,ITALY
关键词
SIGNAL TRANSDUCTION; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; IMMUNOGOLD LABELING; ISOLATED NUCLEI; NUCLEAR MATRIX; FRIEND CELLS; RAT PANCREAS; 3T3; CELLS;
D O I
10.1177/43.2.7822774
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphatidylinositol 4,5-bisphosphate (PIP2) is a key element of signal transduction, being the preferential substrate of specific phospholipases that produce second messengers such as inositol trisphosphate (IP3) and diacylglycerol (DG). Because PIP2 has been cytochemically identified by monoclonal antibodies not only in the cytoplasmic membranes but also in the nuclear envelope and within the nucleus, we performed a study by immunoblotting and by confocal and electron microscopic immunocytochemistry to identify the nuclear sites of PIP2 localization and to exclude any cross-reactivity of the antibody with other nuclear molecules, The results confirm the specificity of the immunolabeling and indicate that PIP2 is localized at precise intranuclear sites both in in situ and in isolated nuclei. They also show that a significant amount of the phospholipid is retained by the cytoskeleton and by the inner nuclear matrix in in situ matrix preparations. Moreover the sensitivity of the immunocytochemical reaction is capable of detecting quantitative variations of PIP2 nuclear content induced by agonists that modulate the signal transduction system at the nuclear level,
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页码:181 / 191
页数:11
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