Nature and severity of the glomerular response to nephron reduction is strain-dependent in mice

被引:66
作者
Esposito, C
He, CJ
Striker, GE
Zalups, RK
Striker, LJ
机构
[1] Univ Miami, Sch Med, Dept Med, Renal Cell Biol Lab, Miami, FL 33101 USA
[2] Univ Pavia, IRCCS, Policlin San Matteo, Div Nephrol, I-27100 Pavia, Italy
[3] Mercer Univ, Sch Med, Div Basic Med Sci, Macon, GA 31207 USA
关键词
D O I
10.1016/S0002-9440(10)65336-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Nephron reduction Is an important factor in the development of glomerulosclerosis. In a study of the oligosyndactyly (Os) mutation that causes a congenital 50% reduction ill nephron number, we previously found that ROP Os/+ mice developed glomerulosclerosis whereas C57B1/6J Os/+ mice did not, We concluded that the predisposition to glomerulosclerosis depended largely on the genetic background, the ROP being sclerosis-prone whereas the C57 strain was sclerosis-resistant, In the current experiments we asked whether the intensity of the sclerotic response to nephron reduction In the ROP strain was related to the time at which it occurred, ie, a pre- or post-natal event. We also determined whether the absence of lesions in C57 Os/+ mice was caused by a higher threshold for the induction of a sclerotic response In C57 mice. We further examined the relationship between glomerular hypertrophy and sclerosis. C57 +/+, C57 Os/+, ROP +/+, and ROP Os/+ mice were uninephrectomized (NX) at age 10 weeks and followed for 8 weeks. We found no sclerotic changes in NX C57 +/+ and C57 Os/+ mice, despite a 75% reduction in nephron number in the latter, In contrast, both NX ROP +/+ and NX ROP Os/+ mice had glomerulosclerosis, which was more severe in the NX ROP Os/+ mice, Examination of extracellular matrix synthesis and degradation at the mRNA level revealed that synthesis exceeded degradation in ROP Os/+ mice. The lesions in NX ROP +/+ were less severe than in sham-operated ROP/Os mice, suggesting that the timing of nephron reduction affected the amplitude of the sclerotic response in this strain, Following NX, an increase in glomerular volume was found in C57 +/+, ROP +/+, and ROP Os/+ mice, However, NX did clot lead to a further increase in glomerular volume in C57 Os/+ mice. We make three conclusions: 1) sclerosis was more severe in the ROP strain when nephron reduction occurred In utero; 2) the absence of glomerulosclerosis in C57 mice was not related to a higher threshold for a sclerosis response in this strain; and 3) whereas glomerular size continued to increase as nephron number decreased in ROP mice, it reached a plateau in C57 mice.
引用
收藏
页码:891 / 897
页数:7
相关论文
共 24 条
  • [1] THE LIVING DONOR IN KIDNEY-TRANSPLANTATION
    BAY, WH
    HEBERT, LA
    [J]. ANNALS OF INTERNAL MEDICINE, 1987, 106 (05) : 719 - 727
  • [2] BIDANI AK, 1993, J LAB CLIN MED, V121, P284
  • [3] NEPHRON ADAPTATION TO RENAL INJURY OR ABLATION
    BRENNER, BM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (03): : F324 - F337
  • [4] Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat
    Brown, DM
    Provoost, AP
    Daly, MJ
    Lander, ES
    Jacob, HJ
    [J]. NATURE GENETICS, 1996, 12 (01) : 44 - 51
  • [5] DOI T, 1990, AM J PATHOL, V137, P541
  • [6] SELECTIVITY OF RENAL INJURY AND PROTEINURIA IN SPONTANEOUSLY HYPERTENSIVE RAT
    FELD, LG
    VANLIEW, JB
    GALASKE, RG
    BOYLAN, JW
    [J]. KIDNEY INTERNATIONAL, 1977, 12 (05) : 332 - 343
  • [7] FLOEGE J, 1992, LAB INVEST, V66, P485
  • [8] GROND J, 1986, LAB INVEST, V54, P77
  • [9] RELATIONSHIPS BETWEEN MESANGIAL CELL-PROLIFERATION AND TYPE-I AND TYPE-IV COLLAGEN MESSENGER-RNA LEVELS IN-VITRO
    HE, CJ
    STRIKER, LJ
    TSOKOS, M
    YANG, CW
    PETEN, EP
    STRIKER, GE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (03): : C554 - C562
  • [10] Dissociation of glomerular hypertrophy, cell proliferation, and glomerulosclerosis in mouse strains heterozygous for a mutation (Os) which induces a 50% reduction in nephron number
    He, CJ
    Esposito, C
    Phillips, C
    Zalups, RK
    Henderson, DA
    Striker, GE
    Striker, LJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (05) : 1242 - 1249