Collagen XVIII regulates extracellular matrix integrity in the developing nephrons and impacts nephron progenitor cell behavior
Rinta-Jaskari, Mia M; Naillat, Florence; Ruotsalainen, Heli J; Ronkainen, Veli-Pekka; Heljasvaara, Ritva; Akram, Saad U; Izzi, Valerio; Miinalainen, Ilkka; Vainio, Seppo J; Pihlajaniemi, Taina A (2024-05-22)
Rinta-Jaskari, Mia M
Naillat, Florence
Ruotsalainen, Heli J
Ronkainen, Veli-Pekka
Heljasvaara, Ritva
Akram, Saad U
Izzi, Valerio
Miinalainen, Ilkka
Vainio, Seppo J
Pihlajaniemi, Taina A
Elsevier
22.05.2024
Mia M. Rinta-Jaskari, Florence Naillat, Heli J. Ruotsalainen, Veli-Pekka Ronkainen, Ritva Heljasvaara, Saad U. Akram, Valerio Izzi, Ilkka Miinalainen, Seppo J. Vainio, Taina A. Pihlajaniemi, Collagen XVIII regulates extracellular matrix integrity in the developing nephrons and impacts nephron progenitor cell behavior, Matrix Biology, Volume 131, 2024, Pages 30-45, ISSN 0945-053X, https://doi.org/10.1016/j.matbio.2024.05.005
https://creativecommons.org/licenses/by/4.0/
© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
https://creativecommons.org/licenses/by/4.0/
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:oulu-202406104301
https://urn.fi/URN:NBN:fi:oulu-202406104301
Tiivistelmä
Abstract
Renal development is a complex process in which two major processes, tubular branching and nephron development, regulate each other reciprocally. Our previous findings have indicated that collagen XVIII (ColXVIII), an extracellular matrix protein, affects the renal branching morphogenesis. We investigate here the role of ColXVIII in nephron formation and the behavior of nephron progenitor cells (NPCs) using isoform-specific ColXVIII knockout mice. The results show that the short ColXVIII isoform predominates in the early epithelialized nephron structures whereas the two longer isoforms are expressed only in the later phases of glomerular formation. Meanwhile, electron microscopy showed that the ColXVIII mutant embryonic kidneys have ultrastructural defects at least from embryonic day 16.5 onwards. Similar structural defects had previously been observed in adult ColXVIII-deficient mice, indicating a congenital origin. The lack of ColXVIII led to a reduced NPC population in which changes in NPC proliferation and maintenance and in macrophage influx were perceived to play a role. The changes in NPC behavior in turn led to notably reduced overall nephron formation. In conclusion, the results show that ColXVIII has multiple roles in renal development, both in ureteric branching and in NPC behavior.
Renal development is a complex process in which two major processes, tubular branching and nephron development, regulate each other reciprocally. Our previous findings have indicated that collagen XVIII (ColXVIII), an extracellular matrix protein, affects the renal branching morphogenesis. We investigate here the role of ColXVIII in nephron formation and the behavior of nephron progenitor cells (NPCs) using isoform-specific ColXVIII knockout mice. The results show that the short ColXVIII isoform predominates in the early epithelialized nephron structures whereas the two longer isoforms are expressed only in the later phases of glomerular formation. Meanwhile, electron microscopy showed that the ColXVIII mutant embryonic kidneys have ultrastructural defects at least from embryonic day 16.5 onwards. Similar structural defects had previously been observed in adult ColXVIII-deficient mice, indicating a congenital origin. The lack of ColXVIII led to a reduced NPC population in which changes in NPC proliferation and maintenance and in macrophage influx were perceived to play a role. The changes in NPC behavior in turn led to notably reduced overall nephron formation. In conclusion, the results show that ColXVIII has multiple roles in renal development, both in ureteric branching and in NPC behavior.
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