TY - JOUR
T1 - The inner nuclear membrane protein NEMP1 supports nuclear envelope openings and enucleation of erythroblasts
AU - Hodzic, Didier
AU - Wu, Jun
AU - Krchma, Karen
AU - Jurisicova, Andrea
AU - Tsatskis, Yonit
AU - Liu, Yijie
AU - Ji, Peng
AU - Choi, Kyunghee
AU - McNeill, Helen
N1 - Publisher Copyright:
© 2022 Authors. All rights reserved.
PY - 2022/10
Y1 - 2022/10
N2 - AU Nuclear: Pleaseconfirmthatallheadinglevelsarerepresentedcorrectly envelope membrane proteins (NEMPs) are a conserved : family of nuclear envelope (NE) proteins that reside within the inner nuclear membrane (INM). Even though Nemp1 knockout (KO) mice are overtly normal, they display a pronounced splenomegaly. This phenotype and recent reports describing a requirement for NE openings during erythroblasts terminal maturation led us to examine a potential role for Nemp1 in erythropoiesis. Here, we report that Nemp1 KO mice show peripheral blood defects, anemia in neonates, ineffective erythropoiesis, splenomegaly, and stress erythropoiesis. The erythroid lineage of Nemp1 KO mice is overrepresented until the pronounced apoptosis of polychromatophilic erythroblasts. We show that NEMP1 localizes to the NE of erythroblasts and their progenitors. Mechanistically, we discovered that NEMP1 accumulates into aggregates that localize near or at the edge of NE openings and Nemp1 deficiency leads to a marked decrease of both NE openings and ensuing enucleation. Together, our results for the first time demonstrate that NEMP1 is essential for NE openings and erythropoietic maturation in vivo and provide the first mouse model of defective erythropoiesis directly linked to the loss of an INM protein.
AB - AU Nuclear: Pleaseconfirmthatallheadinglevelsarerepresentedcorrectly envelope membrane proteins (NEMPs) are a conserved : family of nuclear envelope (NE) proteins that reside within the inner nuclear membrane (INM). Even though Nemp1 knockout (KO) mice are overtly normal, they display a pronounced splenomegaly. This phenotype and recent reports describing a requirement for NE openings during erythroblasts terminal maturation led us to examine a potential role for Nemp1 in erythropoiesis. Here, we report that Nemp1 KO mice show peripheral blood defects, anemia in neonates, ineffective erythropoiesis, splenomegaly, and stress erythropoiesis. The erythroid lineage of Nemp1 KO mice is overrepresented until the pronounced apoptosis of polychromatophilic erythroblasts. We show that NEMP1 localizes to the NE of erythroblasts and their progenitors. Mechanistically, we discovered that NEMP1 accumulates into aggregates that localize near or at the edge of NE openings and Nemp1 deficiency leads to a marked decrease of both NE openings and ensuing enucleation. Together, our results for the first time demonstrate that NEMP1 is essential for NE openings and erythropoietic maturation in vivo and provide the first mouse model of defective erythropoiesis directly linked to the loss of an INM protein.
UR - http://www.scopus.com/inward/record.url?scp=85140855861&partnerID=8YFLogxK
U2 - 10.1371/journal.pbio.3001811
DO - 10.1371/journal.pbio.3001811
M3 - Article
C2 - 36215313
AN - SCOPUS:85140855861
SN - 1544-9173
VL - 20
JO - PLoS biology
JF - PLoS biology
IS - 10
M1 - e3001811
ER -