Three-dimensional visualization of the renal proximal tubules in developing mice

CONG Jing GU Ling ZHANG Jie SONG Ke-xin ZHAI Xia-yue WANG Xiao-jie

Acta Anatomica Sinica ›› 2021, Vol. 52 ›› Issue (5) : 789-794.

PDF(6076 KB)
Welcome to visit Acta Anatomica Sinica! Today is Chinese
PDF(6076 KB)
Acta Anatomica Sinica ›› 2021, Vol. 52 ›› Issue (5) : 789-794. DOI: 10.16098/j.issn.0529-1356.2021.05.018
Histology,Embryology and Developmental Biology

Three-dimensional visualization of the renal proximal tubules in developing mice

  • CONG Jing1,2  GU Ling2  ZHANG Jie2  SONG Ke-xin2  ZHAI Xia-yue2*  WANG Xiao-jie3*
Author information +
History +

Abstract

Objective  Adult proximal tubule (PT) is not only the segment most frequently involved in acute renal tubule injury, but also the easiest to repair. It may be consistent with the rapid growth and differentiation mechanism of this segment during the development of the kidney, while the developing information is insufficient. Therefore, we three-dimensional visualized the developing PT to analysis its spatiotemporal morphogenesis.    Methods  The kidneys were obtained from mice at various developing time point, embryonic day (E), postnatal day (P). The volume density of Claudin-2 positive PT in the cortex was measured using a stereological method  in paraffin sections. After image recording and alignment of the serial sections, the spatial courses of the developing PT were traced and visualized in three dimensions using computer-assisted program. The length of the developing PT was calculated at the same time.    Results  The volume density of PT in the cortex of P1 mice was significantly higher than that in the embryonic stage. Then it experienced a decline (P3, P5), an increase (start at P7) to a stable adult level (P28). The tubular tracing showed that the lengths of developing PT and the number of convolutions of their convoluted part increased with the maturation, but lower than that of adultin E14.5, E17.5 and P5 PT in E14.5 and E17.5 mice were similar to that of adult with respect to general spatial courses. They were, however, significantly different from adult in the initial direction of PT and the arrangement of the straight part of PT in the medullary rays. While, it was in P5 that the spatial pattern of some PT was gradually approaching to the adult model.    Conclusion  This study demonstrated that the development of PT was consistent with the kidney development in terms of its volume density in cortex, length and spatial course. It started at the S-shaped body, kept throughout the embryonic period and continued to postnatal, ended at kidney maturation (P28).

Key words

Kidney / Proximal tubule / Growth and development / Volume density / Three-dimensional reconstruction / Mouse

Cite this article

Download Citations
CONG Jing GU Ling ZHANG Jie SONG Ke-xin ZHAI Xia-yue WANG Xiao-jie. Three-dimensional visualization of the renal proximal tubules in developing mice[J]. Acta Anatomica Sinica. 2021, 52(5): 789-794 https://doi.org/10.16098/j.issn.0529-1356.2021.05.018

References

[1] Rosenthal R, Gunzel D, Krug SM, et al. Claudin-2-mediated cation and water transport share a common pore [J]. Acta Physiol (Oxf), 2017, 219(2): 521-536.
[2] Sun J, Hultenby K, Axelsson J, et al. Proximal tubular expression patterns of megalin and cubilin in proteinuric nephropathies [J]. Kidney Int Rep, 2017, 2(4): 721-732.
[3] Chevalier RL. The proximal tubule is the primary target of injury and progression of kidney disease: role of the glomerulotubular junction [J]. Am J Physiol Renal Physiol, 2016, 311(1): F145-161.
[4] Chang-Panesso M, Kadyrov FF, Lalli M, et al. FOXM1 drives proximal tubule proliferation during repair from acute ischemic kidney injury [J]. J Clin Invest, 2019, 129(12): 5501-5517.
[5] Chambers JM, Wingert RA. Advances in understanding vertebrate nephrogenesis [J]. Tissue Barriers, 2020, 8(4): 1832844.
[6] Lindstr?m NO, De Sena Brandine G, Tran T, et al. Progressive recruitment of mesenchymal progenitors reveals a time-dependent process of cell fate acquisition in mouse and human nephrogenesis [J]. Dev Cell, 2018, 45(5): 651-660.
[7] Ling G, Jing C, Jie Z, et al. A microwave antigen retrieval method using two heating steps for enhanced immunostaining on aldehyde-fixed paraffin-embedded tissue sections [J]. Histochem Cell Biol, 2016, 145(6): 675-680.
[8] Chang SJ, Li S, Andreasen A, et al. A reference-free method for brightness compensation and contrast enhancement of micrographs of serial sections [J]. PLoS One, 2015, 10 (5): e0127855.
[9] Zhang J, Cong J, Yang J, et al. Morphologic and morphometric study on microvasculature of developing mouse kidneys [J]. Am J Physiol Renal Physiol, 2017, 315(4): F852-860.
[10] Den SQ, Gu L, Miao JK, et al. Three-dimensional visualization of the mouse renal distal convoluted tubule[J]. Acta Anatomica Sinica, 2018, 49(5): 636-640. (in Chinese)
邓思琪,顾玲,苗俊珂,等.小鼠肾远曲小管三维可视化研究[J]. 解剖学报, 2018, 49(5): 636-640.
[11] St Pierre TG, House MJ, Bangma SJ, et al. Stereological analysis of liver biopsy histology sections as a reference standard for validating non-invasive liver fat fraction measurements by MRI [J]. PLoS One, 2016, 11(8): e0160789.
[12] Rumballe BA, Georgas KM, Combes AN, et al. Nephron formation adopts a novel spatial topology at cessation of nephrogenesis [J]. Dev Biol, 2011, 360(1): 110-122.
[13] Zhai XY, Birn H, Jensen KB, et al. Digital three-dimensional reconstruction and ultrastructure of the mouse proximal tubule [J]. J Am Soc Nephrol, 2003, 14(3): 611-619.
[14] Inkyo-Hayasaka K, Sakai T, Kobayashi N, et al. Three-dimensional analysis of the whole mesangium in the rat [J]. Kidney Int, 1996, 50(2): 672-683.
[15] D ?rup J. Ultrastructure of the distal nephron. An analysis of structure-function relationships in distal nephron segments of the kidney [J]. Dan Med Bull, 1990, 37(6): 502-506.
[16] Christensen EI, Grann B, Kristoffersen IB, et al. Three-dimensional reconstruction of the rat nephron [J]. Am J Physiol Renal Physiol, 2014, 306(6): F664-F671.
[17] Little MH, Kairath P. Does renal repair recapitulate kidney development [J]? J Am Soc Nephrol, 2017, 28(1): 34-46.
[18] Fanni D, Sanna A, Gerosa C, et al. Each niche has an actor: multiple stem cell niches in the preterm kidney [J]. Ital J Pediatr, 2015, 41:78.
[19] Shrestha S, Somji S, Sens DA, et al. Human renal tubular cells contain CD24/CD133 progenitor cell populations: Implications for tubular regeneration after toxicant induced damage using cadmium as a model [J]. Toxicol Appl Pharmacol, 2017, 331(3): 116-129.
PDF(6076 KB)

Accesses

Citation

Detail

Sections
Recommended

/