Deletion of a flippase subunit Tmem30a in hematopoietic cells impairs mouse fetal liver erythropoiesis

Fan Yang, Yumin Huang, Xianda Chen, Lu Liu, Dandan Liao, Huan Zhang, Gang Huang, Wenjing Liu, Xianjun Zhu, Wengong Wang, Cheryl A. Lobo, Karina Yazdanbakhsh, Xiuli An, Zhenyu Ju

Research output: Contribution to journalArticlepeer-review

2 Scopus citations


Transmembrane protein 30A (Tmem30a) is the β-subunit of P4- ATPases which function as flippase that transports aminophospholipids such as phosphatidylserine from the outer to the inner leaflets of the plasma membrane to maintain asymmetric distribution of phospholipids. It has been documented that deficiency of Tmem30a led to exposure of phosphatidylserine. However, the role of Tmem30a in vivo remains largely unknown. Here we found that Vav-Cre-driven conditional deletion of Tmem30a in hematopoietic cells led to embryonic lethality due to severe anemia by embryonic day 16.5. The numbers of erythroid colonies and erythroid cells were decreased in the Tmem30a deficient fetal liver. This was accompanied by increased apoptosis of erythroid cells. Confocal microscopy analysis revealed an increase of localization of erythropoietin receptor to areas of membrane raft microdomains in response to erythropoietin stimulation in Ter119-erythroid progenitors, which was impaired in Tmem30a deficient cells. Moreover, erythropoietin receptor (EPOR)-mediated activation of the STAT5 pathway was significantly reduced in Tmem30a deficient fetal liver cells. Consistently, knockdown of TMEM30A in human CD34+ cells also impaired erythropoiesis. Our findings demonstrate that Tmem30a plays a critical role in erythropoiesis by regulating the EPOR signaling pathway through the formation of membrane rafts in erythroid cells.

Original languageEnglish (US)
Pages (from-to)1984-1994
Number of pages11
Issue number10
StatePublished - 2019
Externally publishedYes

ASJC Scopus subject areas

  • Hematology


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