» Articles » PMID: 24408873

The Regenerative Potential of Parietal Epithelial Cells in Adult Mice

Overview
Specialty Nephrology
Date 2014 Jan 11
PMID 24408873
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

Previously, we showed that some podocytes in juvenile mice are recruited from cells lining Bowman's capsule, suggesting that parietal epithelial cells (PECs) are a progenitor cell population for podocytes. To investigate whether PECs also replenish podocytes in adult mice, PECs were genetically labeled in an irreversible fashion in 5-week-old mice. No significant increase in labeled podocytes was observed, even after 18 months. To accelerate a potential regenerative mechanism, progressive glomerular hypertrophy was induced by progressive partial nephrectomies. Again, no significant podocyte replenishment was observed. Rather, labeled PECs exclusively invaded segments of the tuft affected by glomerulosclerosis, consistent with our previous findings. We next reassessed PEC recruitment in juvenile mice using a different reporter mouse and confirmed significant recruitment of labeled PECs onto the glomerular tuft. Moreover, some labeled cells on Bowman's capsule expressed podocyte markers, and cells on Bowman's capsule were also directly labeled in juvenile podocyte-specific Pod-rtTA transgenic mice. In 6-week-old mice, however, cells on Bowman's capsule no longer expressed podocyte-specific markers. Similarly, in human kidneys, some cells on Bowman's capsule expressed the podocyte marker synaptopodin from 2 weeks to 2 years of age but not at 7 years of age. In summary, podocyte regeneration from PECs could not be detected in aging mice or models of glomerular hypertrophy. We propose that a small fraction of committed podocytes reside on Bowman's capsule close to the vascular stalk and are recruited onto the glomerular tuft during infancy to adolescence in mice and humans.

Citing Articles

Continuous increase in podocyte numbers in the first 36 months of life-insights from forensic autopsies in Japanese children.

Takashima K, Hitosugi M, Uno A, Taniura N, Mukaisho K, Maruo Y Pediatr Nephrol. 2025; .

PMID: 39792255 DOI: 10.1007/s00467-024-06644-7.


Inhibition of the glucocorticoid receptor attenuates proteinuric kidney diseases in multiple species.

Stamellou E, Agrawal S, Siegerist F, Buse M, Kuppe C, Lange T Nephrol Dial Transplant. 2023; 39(7):1181-1193.

PMID: 38037533 PMC: 11210988. DOI: 10.1093/ndt/gfad254.


Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy.

Braun F, Abed A, Sellung D, Rogg M, Woidy M, Eikrem O J Clin Invest. 2023; 133(11).

PMID: 37014703 PMC: 10232004. DOI: 10.1172/JCI157782.


WT1 glomerular parietal epithelial progenitors promote renal proximal tubule regeneration after severe acute kidney injury.

Hong X, Nie H, Deng J, Liang S, Chen L, Li J Theranostics. 2023; 13(4):1311-1324.

PMID: 36923529 PMC: 10008742. DOI: 10.7150/thno.79326.


Parietal Epithelial Cell Behavior and Its Modulation by microRNA-193a.

Bharati J, Chander P, Singhal P Biomolecules. 2023; 13(2).

PMID: 36830635 PMC: 9953542. DOI: 10.3390/biom13020266.


References
1.
Lin F, Moran A, Igarashi P . Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney. J Clin Invest. 2005; 115(7):1756-64. PMC: 1159127. DOI: 10.1172/JCI23015. View

2.
Smeets B, Moeller M . Parietal epithelial cells and podocytes in glomerular diseases. Semin Nephrol. 2012; 32(4):357-67. DOI: 10.1016/j.semnephrol.2012.06.007. View

3.
Ronconi E, Sagrinati C, Angelotti M, Lazzeri E, Mazzinghi B, Ballerini L . Regeneration of glomerular podocytes by human renal progenitors. J Am Soc Nephrol. 2008; 20(2):322-32. PMC: 2637058. DOI: 10.1681/ASN.2008070709. View

4.
Grouls S, Iglesias D, Wentzensen N, Moeller M, Bouchard M, Kemler R . Lineage specification of parietal epithelial cells requires β-catenin/Wnt signaling. J Am Soc Nephrol. 2011; 23(1):63-72. PMC: 3269917. DOI: 10.1681/ASN.2010121257. View

5.
Guo J, Marlier A, Shi H, Shan A, Ardito T, Du Z . Increased tubular proliferation as an adaptive response to glomerular albuminuria. J Am Soc Nephrol. 2011; 23(3):429-37. PMC: 3294312. DOI: 10.1681/ASN.2011040396. View