Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

Matrix protein glycation impairs agonist-induced intracellular Ca2+ signaling in endothelial cells.

Authors:
Nour B Bishara Marjorie E Dunlop Timothy V Murphy Ian A Darby M A Sharmini Rajanayagam Michael A Hill

J Cell Physiol 2002 Oct;193(1):80-92

Microvascular Biology Group, School of Medical Sciences, RMIT University, Bundoora, Victoria, Australia.

Studies have shown diabetes to be associated with alterations in composition of extracellular matrix and that such proteins modulate signal transduction. The present studies examined if non-enzymatic glycation of fibronectin or a mixed matrix preparation (EHS) alters endothelial cell Ca(2+) signaling following agonist stimulation. Endothelial cells were cultured from bovine aorta and rat heart. To glycate proteins, fibronectin (10 microg/ml), or EHS (2.5 mg/ml) were incubated (37 degrees C, 30 days) with 0.5 M glucose-6-phosphate. Matrix proteins were coated onto cover slips after which cells (10(5) cells/ml) were plated and allowed to adhere for 16 h. For measurement of intracellular Ca(2+), cells were loaded with fura 2 (2 microM) and fluorescence intensity monitored. Bovine cells on glycated EHS showed decreased ability for either ATP (10(-6) M) or bradykinin (10(-7) M) to increase Ca(2+) (i). In contrast, glycated fibronectin did not impair agonist-induced increases in Ca(2+) (i). In the absence of extracellular Ca(2+), ATP elicited a transient increase in Ca(2+) (i) consistent with intracellular release. Re-addition of Ca(2+) resulted in a secondary rise in Ca(2+) (i) indicative of store depletion-mediated Ca(2+) entry. Both phases of Ca(2+) mobilization were reduced in cells on glycated mixed matrix; however, as the ratio of the two components was similar in all cells, glycation appeared to selectively impair Ca(2+) release from intracellular stores. Thapsigargin treatment demonstrated an impaired ability of cells on glycated EHS to increase cytoplasmic Ca(2+) consistent with decreased endoplasmic reticulum Ca(2+) stores. Further support for Ca(2+) mobilization was provided by increased baseline IP(3) levels in cells plated on glycated EHS. Impaired ATP-induced Ca(2+) release could be induced by treating native EHS with laminin antibody or exposing cells to H(2)O(2) (20-200 microM). Glycated EHS impaired Ca(2+) signaling was attenuated by treatment with aminoguanidine or the antioxidant alpha-lipoic acid. The results demonstrate that matrix glycation impairs agonist-induced Ca(2+) (i) increases which may impact on regulatory functions of the endothelium and implicate possible involvement of oxidative stress.

Download full-text PDF

Source
http://dx.doi.org/10.1002/jcp.10153DOI Listing
October 2002

Publication Analysis

Top Keywords

ca2+
18
glycated ehs
16
ca2+ signaling
12
cells glycated
12
cells
10
ca2+ mobilization
8
ca2+ release
8
matrix proteins
8
ca2+ consistent
8
intracellular ca2+
8
mixed matrix
8
endothelial cells
8
glycation impairs
8
increase ca2+
8
impairs agonist-induced
8
ehs impaired
8
ehs
7
matrix
6
glycated
6
reticulum ca2+
4

Keyword Occurance

Similar Publications

The N2A region of titin has a unique structural configuration.

Authors:
Chiara Stronczek Stephan Lange Belinda Bullard Sebastian Wolniak Emma Börgeson Olga Mayans Jennifer R Fleming

J Gen Physiol 2021 Jul;153(7)

Department of Biology, University of Konstanz, Konstanz, Germany.

The N2A segment of titin is a main signaling hub in the sarcomeric I-band that recruits various signaling factors and processing enzymes. It has also been proposed to play a role in force production through its Ca2+-regulated association with actin. However, the molecular basis by which N2A performs these functions selectively within the repetitive and extensive titin chain remains poorly understood. Read More

View Article and Full-Text PDF
July 2021
Similar Publications

Effects of aging on proteasomal-ubiquitin system, oxidative stress balance and calcium homeostasis in middle-aged female rat colon.

Authors:
N Almási Z Murlasits A Al-Awar Á Csonka S Dvorácskó C Tömböly S Török D Bester A Pósa C Varga K Kupai

Physiol Int 2021 Apr 8. Epub 2021 Apr 8.

1Department of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.

Aging is a multifactorial process, which is considered as a decline over time. It is increasingly clear that there is a gender difference in aging and in the prevalence of age-related diseases as well. We aimed to examine the effects of the aging process in the colonic tissue of female Wistar rats aged 10 weeks (young) and 13 months (middle-aged) at an early stage, according to three main symptoms associated with aging: a decrease in the efficacy of the proteasome and muscle function and an increase in oxidative stress. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Performance and mechanism of oxidation, and removal of trace SeO in flue gas utilizing a HO, NaClO, and Ca slurry.

Authors:
Jingxiang Ma Yi Zhao Yanan Wei

Environ Sci Pollut Res Int 2021 Apr 8. Epub 2021 Apr 8.

Hebei Key Lab of Power Plant Flue Gas Multi-Pollutants Control, Department of Environmental Science and Engineering, North China Electric Power University, Baoding, 071003, People's Republic of China.

Selenium (Se) is one of the toxic trace elements in flue gas emitted from coal-fired power plants. A method for oxidation and absorption of selenium dioxide (SeO) by hydrogen peroxide (HO) and sodium chlorite (NaClO) in a calcium-based slurry is proposed, in which hydrated lime (Ca(OH)) and calcium carbonate (CaCO) were selected to be absorbents, and HO and NaClO were used to oxidize SeO and selenite ion to selenate ion to reduce their toxicities. The effects of reaction temperature, HO and NaClO concentrations, solution pH, and SeO concentration were investigated, from which the optimal reaction conditions were established. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

The Use of Fluorescently Labeled ARC1779 Aptamer for Assessing the Effect of H2O2 on von Willebrand Factor Exocytosis.

Authors:
Piotr P Avdonin Sergey K Trufanov Elena Yu Rybakova Aleksandra A Tsitrina Nikolay V Goncharov Pavel V Avdonin

Biochemistry (Mosc) 2021 Feb;86(2):123-131

Koltsov Institute of Developmental Biology, Russian Academy of Sciences, Moscow, 119334, Russia.

Here, we propose a new approach for quantitative estimation of von Willebrand factor (vWF) exposed on the surface of endothelial cells (ECs) using the ARC1779 aptamer that interacts with the vWF A1 domain. To visualize complex formation between vWF and the aptamer, the latter was conjugated with the Cy5 fluorescent label. Cultured human umbilical vein endothelial cells (HUVEC) were stained with the ARC1779-Cy5 conjugate and imaged with a fluorescence microscope. Read More

View Article and Full-Text PDF
February 2021
Similar Publications

Regulation of the tubulin polymerization-promoting protein by Ca/S100 proteins.

Authors:
Seita Doi Naoki Fujioka Satomi Ohtsuka Rina Kondo Maho Yamamoto Miwako Denda Masaki Magari Naoki Kanayama Naoya Hatano Ryo Morishita Takafumi Hasegawa Hiroshi Tokumitsu

Cell Calcium 2021 Mar 27;96:102404. Epub 2021 Mar 27.

Applied Cell Biology, Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University, Okayama 700-8530, Japan. Electronic address:

To elucidate S100 protein-mediated signaling pathways, we attempted to identify novel binding partners for S100A2 by screening protein arrays carrying 19,676 recombinant glutathione S-transferase (GST)-fused human proteins with biotinylated S100A2. Among newly discovered putative S100A2 interactants, including TMLHE, TRH, RPL36, MRPS34, CDR2L, OIP5, and MED29, we identified and characterized the tubulin polymerization-promoting protein (TPPP) as a novel S100A2-binding protein. We confirmed the interaction of TPPP with Ca/S100A2 by multiple independent methods, including the protein array method, S100A2 overlay, and pulldown assay in vitro and in transfected COS-7 cells. Read More

View Article and Full-Text PDF
March 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap