Document 0269 DOCN M95A0269 TI Human immunodeficiency virus-1 gp120 and gp160 envelope proteins modulate mesangial cell gelatinolytic activity. DT 9510 AU Singhal PC; Sagar S; Chandra D; Garg P; Department of Medicine, Long Island Jewish Medical Center, New; Hyde Park, New York 11040, USA. SO Am J Pathol. 1995 Jul;147(1):25-32. Unique Identifier : AIDSLINE MED/95328620 AB Patients with human immunodeficiency virus (HIV) infection often develop glomerular lesions (mesangial expansion and sclerosis). Modulation of matrix degradation may be important in the expansion of the mesangium. We studied the effect of HIV sera and HIV-1 envelope glycoproteins on gelatinolytic activity of human mesangial cells. HIV serum-treated cells showed lower (P < 0.01) gelatinolytic activity when compared with cells treated with control serum (control serum, 4.3 +/- 0.1 versus HIV serum, 3.3 +/- 0.1 micrograms gelatin degraded/mg protein). Mesangial cells incubated with HIV-1 gp120 protein also showed decreased (P < 0.01) gelatinolytic activity (control, 4.6 +/- 0.2 versus HIV-1 gp120 protein, 1.7 +/- 0.2 micrograms gelatin degraded/mg protein). HIV-1 gp160 protein also inhibited (P < 0.05) mesangial cell gelatinolytic activity as judged by a biotin-avidin assay as well as by a 3H gelatin degradation assay. In contrast, gp alpha-1 acid, a nonviral glycoprotein, did not modulate mesangial cell gelatinolytic activity. These results suggest that the serum contents of HIV patients decrease gelatinolytic activity of mesangial cells. This effect of HIV sera seems to be mediated through HIV-1 gp proteins. DE Acquired Immunodeficiency Syndrome/BLOOD Cells, Cultured Cytokines/BLOOD Dose-Response Relationship, Drug Extracellular Matrix/METABOLISM Gelatin/*METABOLISM Gelatinases/*METABOLISM Gene Products, env/*PHARMACOLOGY Glomerular Mesangium/CYTOLOGY/DRUG EFFECTS/*METABOLISM Human HIV Antibodies/ANALYSIS HIV Envelope Protein gp120/*PHARMACOLOGY HIV Infections/BLOOD *HIV-1 Protein Precursors/*PHARMACOLOGY Serum Albumin/ANALYSIS Support, U.S. Gov't, P.H.S. Viral Proteins/PHARMACOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).