Induced pluripotent stem cells provide mega insights into kidney disease.

Abstract:

:Rare mutations in the LRP2 gene encoding for the endocytic receptor megalin cause developmental abnormalities and kidney disease. However, the mechanisms governing the dysfunction of mutant megalin remain unclear. A new study utilizing patient-derived induced pluripotent stem cells is now putting the endolysosomal system into the spotlight, as it is proposed to play a central role in the regulation of megalin in health and disease.

journal_name

Kidney Int

journal_title

Kidney international

authors

Luciani A,Freedman BS

doi

10.1016/j.kint.2020.04.033

subject

Has Abstract

pub_date

2020-07-01 00:00:00

pages

54-57

issue

1

eissn

0085-2538

issn

1523-1755

pii

S0085-2538(20)30511-1

journal_volume

98

pub_type

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