Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/2607
Title: Studies on nuclear localization of eNOS in mammalian cells
Researcher: Lakshmanan, Vasudha
Guide(s): Kale, V P
Keywords: Biochemical, Biotechnology, Cell Science
Upload Date: 2-Sep-2011
University: University of Pune
Completed Date: July, 2008
Abstract: Targeting of eNOS into various sub-cellular locations within the cells plays an important role in human physiology. We have addressed the following questions in this study: a) whether eNOS localization into the nuclei of human cells was a major mode of its regulation or was it only a minor and a specialized mode of regulation that takes place in exceptional cases; b) what were the possible molecular attributes of the eNOS protein that effect its distribution between the nuclear and the cytoplasmic compartments of the cell; and c) what physiological consequences might ensue with a disturbed nuclear distribution of eNOS within the cellular environment. We made an important and a novel observation that eNOS was present in the nuclei of several types of human cells, both normal and cancerous, under conditions of a steady state growth in cell culture and our data clearly suggest that its function in this compartment must be taken into consideration while interpreting its role in the physiology of vascular, cardiac, renal and other systems. The characterization of eNOS protein from the purified nuclei revealed that the nuclear eNOS was largely phosphorylated at the Threonine-495 residue and existed predominantly as a monomer. A major fraction of the nuclear eNOS was associated with nuclear speckles, thought to contain spliceosomes and to be involved in the RNA-metabolism. Association of eNOS with spliceosomes/speckled bodies was specific, because it was found to be physically associated with a splicing factor, SC- 35. We demonstrated that the nuclear eNOS retained its ability to generate NO in vitro when supplemented with the necessary cofactors and substrates. The kinetics of NO-generation from the extracts of purified nuclei showed distinct signatures of enzyme-activation in vitro in a temporal sequence and indicated that the eNOS present in the nuclei may not have been primed to generate optimal amounts of NO.
Pagination: 204p.
URI: http://hdl.handle.net/10603/2607
Appears in Departments:National Centre for Cell Science

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File130.85 kBAdobe PDFView/Open
02_certificate.pdf35.78 kBAdobe PDFView/Open
03_declaration.pdf33.89 kBAdobe PDFView/Open
04_acknowledgements.pdf36.93 kBAdobe PDFView/Open
05_table of contents.pdf6.31 kBAdobe PDFView/Open
06_abbreviations.pdf112.14 kBAdobe PDFView/Open
07_abstract.pdf99.83 kBAdobe PDFView/Open
08_chapter 1.pdf158.75 kBAdobe PDFView/Open
09_chapter 2.pdf892.11 kBAdobe PDFView/Open
10_chapter 3.pdf401 kBAdobe PDFView/Open
11_chapter 4.pdf5.79 MBAdobe PDFView/Open
12_chapter 5.pdf919.01 kBAdobe PDFView/Open
13_chapter 6.pdf102.99 kBAdobe PDFView/Open
14_references.pdf225.79 kBAdobe PDFView/Open
15_appendix.pdf161.58 kBAdobe PDFView/Open


Items in Shodhganga are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: