The capacity of mesangial cells (MC) to produce catecholamines (CAs) has been investigated in our laboratory. To study the CA cascade, it is necessary to examine some steps in their metabolic pathway. Tyrosine hydroxylase (TH) catalyzes the rate-limiting step in the biosynthesis of these biogenic am
THE EFFECT OF VARIOUS FORMS OF HEPARIN ON THE RELEASE OF IMMUNE COMPLEXES FROM THE SURFACE OF CULTURED MESANGIAL CELLS
โ Scribed by DRAKELEY, SIMON J.; FURNESS, PETER N.
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 472 KB
- Volume
- 178
- Category
- Article
- ISSN
- 0022-3417
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โฆ Synopsis
Heparin is capable of enhancing the rate of release of antigen from nephritic rat kidneys. It also interferes with the binding of immune complexes by cultured glomernlar mesangial cells. Postulating that these two effects might be related, we sought to determine what basic aspects of the molecular structure of heparin are responsible for the interference with binding in vitrw. After cultured mesangial cells had bound radiolabelled synthetic immune complexes, heparin or a variety of structurally related molecules were added to the supernatant. De-N-snlphated heparin, heparan sulphate, low molecular weight heparin, and low molecular weight dextran sulphate had no effect on immune complex binding. High molecular weight dextran snlphate was able, like heparin, to dislodge immune complexes from mesangial cells, suggesting that high molecular weight and high snlphation are required. These results differ from previous findings in vivo, suggesting that the effect of heparin in vivo is not due to interaction at the mesangial cell surface. Alternative explanations for the effect of heparin in the intact animal include destabilization of the immune complex structure or, more probably, an effect a t the boundary between the immune complex deposit and the basement membrane.
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