PMID- 12372952 OWN - NLM STAT- MEDLINE DCOM- 20030312 LR - 20171101 IS - 1660-8151 (Print) IS - 1660-8151 (Linking) VI - 92 IP - 3 DP - 2002 TI - In vitro effects of Habu snake venom on cultured mesangial cells. PG - 665-72 AB - BACKGROUND: Habu snake venom (HSV)-induced glomerulonephritis is a unique model showing a progressive course of mesangial proliferation. To elucidate the in vitro effects of HSV, we examined whether HSV itself could have direct effects on the cultured mesangial cells, such as cell proliferation and activation of chemokine gene expression. METHODS: The incorporation of 5-[(125)I]iodo-2'-deoxyuridine was measured with a gamma-counter, and gene expressions of growth factors, chemokines and cytokines were evaluated by a real time quantitative PCR. RESULTS: We demonstrated that excessive or continuous HSV stimulation decreased a mesangial cell viability. However, adequate and temporary HSV stimulation induced proliferation of mesangial cells in vitro along with a significant elevation of monocyte chemoattractant protein-1 (MCP-1) mRNA levels. In addition to these in vitro results, we showed that MCP-1 mRNA levels increased in renal cortices of glomerulonephritis induced by HSV. Immunohistochemistry also showed a positive staining for MCP-1 in the marginal area of glomerulus with mesangiolysis. CONCLUSIONS: These data suggest that HSV itself may elicit direct biological effects on mesangial cells which may participate in pathophysiology of glomerulonephritis induced by HSV. CI - Copyright 2002 S. Karger AG, Basel FAU - Kubo, Atsushi AU - Kubo A AD - Department of Public Health, Nara Medical University, Kashihara, Nara, Japan. FAU - Iwano, Masayuki AU - Iwano M FAU - Kobayashi, Yoshiyuki AU - Kobayashi Y FAU - Kyoda, Yusuke AU - Kyoda Y FAU - Isumi, Yoshitaka AU - Isumi Y FAU - Maruyama, Naoki AU - Maruyama N FAU - Samejima, Kenichi AU - Samejima K FAU - Dohi, Yoshiko AU - Dohi Y FAU - Minamino, Naoto AU - Minamino N FAU - Yonemasu, Kunio AU - Yonemasu K LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Switzerland TA - Nephron JT - Nephron JID - 0331777 RN - 0 (Chemokine CCL2) RN - 0 (Crotalid Venoms) RN - 0 (Growth Substances) RN - 0 (Interleukin-1) RN - 0 (RNA, Messenger) RN - 0 (Tumor Necrosis Factor-alpha) RN - 9007-49-2 (DNA) SB - IM MH - Animals MH - Cell Division/drug effects MH - Cell Survival/drug effects MH - Cells, Cultured MH - Chemokine CCL2/analysis/genetics MH - Crotalid Venoms/*pharmacology MH - DNA/biosynthesis MH - Gene Expression/drug effects MH - Glomerular Mesangium/chemistry/*cytology/drug effects MH - Glomerulonephritis, Membranoproliferative/*chemically induced/pathology/physiopathology MH - Growth Substances/genetics MH - Immunohistochemistry MH - In Vitro Techniques MH - Interleukin-1/genetics MH - Macrophages/cytology/drug effects MH - Male MH - RNA, Messenger/analysis MH - Rats MH - Rats, Wistar MH - Trimeresurus MH - Tumor Necrosis Factor-alpha/genetics EDAT- 2002/10/10 04:00 MHDA- 2003/03/13 04:00 CRDT- 2002/10/10 04:00 PHST- 2002/10/10 04:00 [pubmed] PHST- 2003/03/13 04:00 [medline] PHST- 2002/10/10 04:00 [entrez] AID - 64115 [pii] AID - 10.1159/000064115 [doi] PST - ppublish SO - Nephron. 2002;92(3):665-72. doi: 10.1159/000064115.