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1.
J Neuroimmunol ; 106(1-2): 14-22, 2000 Jul 01.
Article in English | MEDLINE | ID: mdl-10814778

ABSTRACT

Various lines of evidence suggest a close relationship between heat shock proteins (hsp) and several autoimmune diseases such as arthritis, diabetes and multiple sclerosis. While enhanced expression of hsp in autoimmune diseases is often regarded as a non-specific bystander effect of the inflammatory process, surprisingly little is known on hsp regulation by inflammatory mediators such as cytokines. In this study cytokine-induced expression of hsp60, hsp27 and alphaB-crystallin was studied in cultures of primary human adult astrocytes at the mRNA as well as at the protein level. We show differential hsp expression patterns in response to pro-inflammatory and immunoregulatory cytokines. Hsp60 expression was found to be enhanced in response to cytokines as diverse as IL-1beta, TNF-alpha, IL-4, IL-6 and IL-10. Upregulation of hsp27, however, was primarily induced by immunoregulatory cytokines like IL-4, IL-6 and TGF-beta whereas alphaB-crystallin expression was found to be enhanced by the pro-inflammatory cytokine TNF-alpha only. None of the cytokines studied was able to enhance expression of all three hsp simultaneously. These results show that in human astrocytes induced expression of hsp27 and alphaB-crystallin is dependent on the presence of a defined set of stimuli, while induced expression of hsp60 is a much less selective event. This highly differential pattern of hsp expression in response to inflammatory mediators known to play an important role in the pathogenesis of autoimmune diseases indicates that hsp responses are specific rather than non-specific bystander responses.


Subject(s)
Astrocytes/metabolism , Cytokines/pharmacology , Heat-Shock Proteins/metabolism , Adjuvants, Immunologic/pharmacology , Aged , Aged, 80 and over , Cells, Cultured , Chaperonin 60/genetics , Crystallins/genetics , Female , Heat-Shock Proteins/genetics , Humans , Inflammation Mediators/pharmacology , Male , Middle Aged , RNA, Messenger/metabolism , Up-Regulation
2.
Cell Stress Chaperones ; 5(1): 30-5, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10701837

ABSTRACT

We describe a reverse transcriptase-polymerase chain reaction method for the semiquantitative detection of mRNAs encoding the human heat shock proteins alphaB-crystallin, Hsp27, and Hsp60. The method involves the coamplification of cellular mRNA-derived cDNA with a dilution series of a competitor fragment (internal standard), using 1 primer pair common to both templates. Internal standards were based on cellular-derived cDNA engineered to be slightly smaller to differentiate between the target and the standard on electrophoretic separation. Initial cDNA quantitations can be corrected for possible variations during cDNA synthesis by standardizing to the levels of beta-actin-encoding cDNA. We show that the coamplified templates accumulate in a parallel manner with the cellular-derived cDNA throughout both the exponential and the nonexponential phase of amplification. Furthermore, we illustrate the utility of this technique by quantifying increased expression of alphaB-crystallin, Hsp27, and Hsp60 mRNA in astroglioma cells on heat shock.


Subject(s)
Chaperonin 60/genetics , Crystallins/genetics , Heat-Shock Proteins , Hot Temperature , Neoplasm Proteins/genetics , RNA, Messenger/analysis , Reagent Kits, Diagnostic , Reverse Transcriptase Polymerase Chain Reaction , Stress, Physiological/genetics , Astrocytoma/pathology , Binding, Competitive , Brain Neoplasms/pathology , DNA, Complementary/genetics , HSP27 Heat-Shock Proteins , Humans , Molecular Chaperones , Neoplasm Proteins/biosynthesis , RNA, Messenger/genetics , RNA, Neoplasm/biosynthesis , RNA, Neoplasm/genetics , Stress, Physiological/metabolism , Tumor Cells, Cultured
3.
Pharm Weekbl Sci ; 11(5): 175-8, 1989 Oct 20.
Article in English | MEDLINE | ID: mdl-2594469

ABSTRACT

Severe, massive bladder haemorrhage is a difficult and often frustrating clinical problem. The aetiologies are numerous and include irradiation, malignancy, severe infection and drug-induced changes. Among the numerous modalities of treatment that have been reported formalin, phenol and silver nitrate instillations have often been associated with significant side effects, morbidity and mortality and have had varying degrees of success. During the last two years we have used continuous closed irrigation of a sterile 0.5% alum solution in 16 patients. Alum is an astringent and acts by protein precipitation over the bleeding surface. Because of a low cell permeability its action is limited to the cell surface and interstitial spaces. The permeability of the cell membrane is reduced but remains viable. The preparation and the pharmaceutical aspects of the 0.5% alum irrigation will be discussed. The conclusion is that the technique of managing massive bladder haemorrhage is simple, efficient, nontoxic and less expensive than previously reported therapies. Therefore, irrigation with alum before instituting invasive means to control bleeding is recommended.


Subject(s)
Alum Compounds/therapeutic use , Aluminum/therapeutic use , Hemorrhage/therapy , Urinary Bladder Diseases/therapy , Aged , Female , Formaldehyde/therapeutic use , Hemorrhage/chemically induced , Humans , Male , Middle Aged , Phenols/therapeutic use , Silver Nitrate/therapeutic use , Therapeutic Irrigation , Urinary Bladder Diseases/chemically induced
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