Immunocytochemical detection of phosphatidylinositol 4,5-bisphosphate localization sites within the nucleus

• Published in: The journal of histochemistry and cytochemistry 1995-02, Vol.43 (2), p.181-191
• Main Authors: Mazzotti, G, Zini, N, Rizzi, E, Rizzoli, R, Galanzi, A, Ognibene, A, Santi, S, Matteucci, A, Martelli, AM, Maraldi, NM
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Animals; Cell Nucleus - chemistry; Cross Reactions; Histones - immunology; Immunoblotting; Mice; Microscopy, Confocal; Microscopy, Immunoelectron; Nuclear Matrix - chemistry; Phosphotransferases (Alcohol Group Acceptor) - analysis; Phosphotransferases (Alcohol Group Acceptor) - immunology; Precipitin Tests; Tumor Cells, Cultured
• ISSN: 0022-1554; 1551-5044
• DOI: 10.1177/43.2.7822774

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.