Cellular Origins of Type IV Collagen Networks in Developing Glomeruli

被引:156
作者
Abrahamson, Dale R. [1 ,2 ]
Hudson, Billy G. [3 ,4 ]
Stroganova, Larysa [1 ,2 ]
Borza, Dorin-Bogdan [3 ,4 ]
John, Patricia L. St. [1 ,2 ]
机构
[1] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Kidney Inst, Kansas City, KS 66160 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[4] Vanderbilt Univ, Med Ctr, Ctr Matrix Biol, Nashville, TN USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2009年 / 20卷 / 07期
基金
美国国家卫生研究院;
关键词
BASEMENT-MEMBRANE; ALPORT-SYNDROME; STEM-CELLS; MOUSE MODEL; DIFFERENTIAL EXPRESSION; MONOCLONAL-ANTIBODIES; CONGENITAL NEPHROSIS; KIDNEY-DISEASE; MICE; PODOCYTES;
D O I
10.1681/ASN.2008101086
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Laminin and type IV Collagen composition of the glomerular basement membrane changes during glomerular development and maturation. Although it is known that both glomerular endothelial cells and podocytes produce different laminin isoforms at the appropriate stages of development, the cellular origins for the different type IV Collagen heterotrimers that appear during development are unknown. Here, immunoelectron microscopy demonstrated that endothelial cells, mesangial cells, and podocytes of immature glomeruli synthesize collagen alpha 1 alpha 2 alpha 1(IV). However, intracellular labeling revealed that podocytes, but not endothelial or mesangial cells, contain collagen alpha 3 alpha 4 alpha 5(IV). To evaluate the origins of Collagen IV further, we transplanted embryonic kidneys from Col4a3-null mutants (Alport mice) into kidneys of newborn, wildtype mice. Hybrid glomeruli within grafts containing numerous host-derived, wildtype endothelial cells never expressed collagen alpha 3 alpha 4 alpha 5(IV). Finally, confocal microscopy of glomeruli from infant Alport mice that had been dually labeled with anti-collagen alpha 5(IV) and the podocyte marker anti-GLEPP1 showed immunolabeling exclusively within podocytes. Together, these results indicate that collagen alpha 3 alpha 4 alpha 5(IV) originates solely from podocytes; therefore, glomerular Alport disease is a genetic defect that manifests specifically within this cell type.
引用
收藏
页码:1471 / 1479
页数:9
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