Anti-Proliferative Actions of T-Type Calcium Channel Inhibition in Thy1 Nephritis

被引:17
作者
Cove-Smith, Andrea [1 ]
Mulgrew, Christopher J. [1 ]
Rudyk, Rena [3 ]
Dutt, Neelanjana [2 ]
McLatchie, Linda M. [3 ]
Shattock, Michael J. [3 ]
Hendry, Bruce M. [1 ]
机构
[1] Kings Coll London, Dept Renal Med, London SE5 9PJ, England
[2] Kings Coll London, Dept Histopathol, London, England
[3] Kings Coll London, St Thomas Hosp, Rayne Inst, Div Cardiovasc, London, England
基金
英国医学研究理事会;
关键词
MESANGIAL CELL-PROLIFERATION; RATS; MYOCYTES; KIDNEY; PROGRESSION; BLOCKERS; INJURY;
D O I
10.1016/j.ajpath.2013.04.029
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aberrant proliferation of mesangial cells (MCs) is a key finding in progressive glomerular disease. TH1177 is a small molecule that has been shown to inhibit low-voltage activated T-type Ca2+ channels (TCCs). The current study investigates the effect of TH1177 on MC proliferation in vitro and in vivo. The effect of Ca2+ channel inhibition on primary rat MC proliferation in vitro was studied using the microculture tetrazolium assay and by measuring bromodeoxyuridine incorporation. In vivo, rats with Thy1 nephritis were treated with TH1177 or vehicle. Glomerular injury and average glomerular cell number were determined in a blinded fashion. Immunostaining for Ki-67 and phosphorylated ERK were also performed. The expression of TCC isoforms in healthy and diseased tissue was investigated using quantitative real-time PCR. TCC blockade caused a significant reduction in rat MC proliferation in vitro, whereas L-type inhibition had no effect. Treatment of Thy1 nephritis with TH1177 significantly reduced glomerular injury (P < 0.005) and caused a 49% reduction in glomerular cell number (P < 0.005) compared to the placebo. TH1177 also reduced Ki-67-positive and pERK-positive cells per glomerulus by 52% (P < 0.01 and P < 0.005, respectively). These results demonstrate that TH1177 inhibits MC proliferation in vitro and in vivo, supporting the hypothesis that TCC inhibition may be a useful strategy for studying and modifying MC proliferative responses to injury.
引用
收藏
页码:391 / 401
页数:11
相关论文
共 26 条
[1]  
AGUAS AP, 1983, AM J PATHOL, V110, P48
[2]   Comparison of L-type and mixed L- and T-type calcium channel blockers on kidney injury caused by deoxycorticosterone-salt hypertension in rats [J].
Baylis, C ;
Qiu, CB ;
Engels, K .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (06) :1292-1297
[3]   In vivo identification of the mitogen-activated protein kinase cascade as a central pathogenic pathway in experimental mesangioproliferative glomerulonephritis [J].
Bokemeyer, D ;
Panek, D ;
Kramer, HJ ;
Lindemann, M ;
Kitahara, M ;
Boor, P ;
Kerjaschki, D ;
Trzaskos, JM ;
Floege, J ;
Ostendorf, T .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (06) :1473-1480
[4]  
Brooks GHJ, 1999, CIRCULATION, V100, P1
[5]   Ras antagonist farnesylthiosalicylic acid (FTS) reduces glomerular cellular proliferation and macrophage number in rat Thy-1 nephritis [J].
Clarke, HC ;
Kocher, HM ;
Khwaja, A ;
Kloog, Y ;
Cook, HT ;
Hendry, BM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (04) :848-854
[6]   INFUSION OF PLATELET-DERIVED GROWTH-FACTOR OR BASIC FIBROBLAST GROWTH-FACTOR INDUCES SELECTIVE GLOMERULAR MESANGIAL CELL-PROLIFERATION AND MATRIX ACCUMULATION IN RATS [J].
FLOEGE, J ;
ENG, E ;
YOUNG, BA ;
ALPERS, CE ;
BARRETT, TB ;
BOWENPOPE, DF ;
JOHNSON, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2952-2962
[7]   EFFECTS OF DIFFERENT ANTIHYPERTENSIVE TREATMENTS ON MORPHOLOGIC PROGRESSION OF DIABETIC NEPHROPATHY IN UNINEPHRECTOMIZED DOGS [J].
GABER, L ;
WALTON, C ;
BROWN, S ;
BAKRIS, G .
KIDNEY INTERNATIONAL, 1994, 46 (01) :161-169
[8]   Cell cycle-related changes in the voltage-gated Ca2+ currents in cultured newborn rat ventricular myocytes [J].
Guo, W ;
Kamiya, K ;
Kodama, I ;
Toyama, T .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (06) :1095-1103
[9]  
Haverstick DM, 2000, CANCER RES, V60, P1002
[10]   Progression of chronic kidney disease: Can it be prevented or arrested? [J].
Jaber, BL ;
Madias, NE .
AMERICAN JOURNAL OF MEDICINE, 2005, 118 (12) :1323-1330