TY - JOUR
T1 - Nephron-Specific Lin28A Overexpression Triggers Severe Inflammatory Response and Kidney Damage
AU - Futorian, Anna
AU - Armon, Leah
AU - Ben-Asher, Hiba Waldman
AU - Shoval, Irit
AU - Hazut, Inbal
AU - Munitz, Ariel
AU - Urbach, Achia
N1 - Publisher Copyright:
© The author(s).
PY - 2024
Y1 - 2024
N2 - The RNA-binding proteins LIN28A and LIN28B contribute to a variety of developmental biological processes. Dysregulation of Lin28A and Lin28B expression is associated with numerous types of tumors. This study demonstrates that Lin28A overexpression in the mouse nephrons leads to severe inflammation and kidney damage rather than to tumorigenesis. Notably, Lin28A overexpression causes inflammation only when expressed in nephrons, but not in the stromal cells of the kidneys, highlighting its cell context-dependent nature. The nephron-specific Lin28A-induced inflammatory response differs from previously described Lin28B-mediated inflammatory feedback loops as it is IL-6 independent. Instead, it is associated with the rapid upregulation of cytokines like Cxcl1 and Ccl2. These findings suggest that the pathophysiological effects of Lin28A overexpression extend beyond cell transformation. Our transgenic mouse model offers a valuable tool for advancing our understanding of the pathophysiology of acute kidney injury, where inflammation is a key factor.
AB - The RNA-binding proteins LIN28A and LIN28B contribute to a variety of developmental biological processes. Dysregulation of Lin28A and Lin28B expression is associated with numerous types of tumors. This study demonstrates that Lin28A overexpression in the mouse nephrons leads to severe inflammation and kidney damage rather than to tumorigenesis. Notably, Lin28A overexpression causes inflammation only when expressed in nephrons, but not in the stromal cells of the kidneys, highlighting its cell context-dependent nature. The nephron-specific Lin28A-induced inflammatory response differs from previously described Lin28B-mediated inflammatory feedback loops as it is IL-6 independent. Instead, it is associated with the rapid upregulation of cytokines like Cxcl1 and Ccl2. These findings suggest that the pathophysiological effects of Lin28A overexpression extend beyond cell transformation. Our transgenic mouse model offers a valuable tool for advancing our understanding of the pathophysiology of acute kidney injury, where inflammation is a key factor.
UR - http://www.scopus.com/inward/record.url?scp=85200939251&partnerID=8YFLogxK
U2 - 10.7150/ijbs.97434
DO - 10.7150/ijbs.97434
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C2 - 39113694
AN - SCOPUS:85200939251
SN - 1449-2288
VL - 20
SP - 4044
EP - 4054
JO - International Journal of Biological Sciences
JF - International Journal of Biological Sciences
IS - 10
ER -