Brief Report: Serpin Spi2A as a Novel Modulator of Hematopoietic Progenitor Cell Formation. (September 2014)

• Record Type: Journal Article
• Authors: Li, Lei; Byrne, Susan M.; Rainville, Nicole; Su, Su; Jachimowicz, Edward; Aucher, Anne; Davis, Daniel M.; Ashton‐Rickardt, Philip G.; Wojchowski, Don M.
• Is Part Of: Stem cells. Volume 32:Number 9(2014:Sep.)
• Page Start: 2550
• Page End: 2556
• Publication Date: 2014-09
• Subjects: Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.1778
• Languages: English
• ISSNs: 1066-5099

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <p>Prime regulation over hematopoietic progenitor cell (HPC) production is exerted by hematopoietins (HPs) and their Janus kinase‐coupled receptors (HP‐Rs). For HP/HP‐R studies, one central challenge in determining specific effects involves the delineation of nonredundant signal transduction factors and their lineage restricted actions. Via loss‐of‐function studies, we define roles for an HP‐regulated <italic>Serpina3g</italic>/Spi2A intracellular serpin during granulomyelocytic, B‐cell, and hematopoietic stem cell (HSC) formation. In granulomyelocytic progenitors, granulocyte macrophage colony stimulating factor (GMCSF) strongly induced <italic>Serpina3g</italic> expression with Stat5 dependency. Spi2A‐knockout (KO) led to 20‐fold decreased CFU‐GM formation, limited GMCSF‐dependent granulocyte formation, and compromised neutrophil survival upon tumor necrosis factor alpha (TNF‐α) exposure. In B‐cell progenitors, Serpina3g was an interleukin‐7 (IL7) target. Spi2A‐KO elevated CFU‐preB greater than sixfold and altered B‐cell formation in competitive bone marrow transplant (BMT), and CpG challenge experiments. In HSCs, <italic>Serpina3g</italic>/Spi2A expression was also elevated. Spi2A‐KO compromised LT‐HSC proliferation (as well as lineage<sup>neg</sup> Sca1<sup>pos</sup> Kit<sup>pos</sup> (LSK) cell lysosomal integrity), and skewed LSK recovery post 5‐FU. Spi2A therefore functions to modulate HP‐regulated immune cell and HSC formation post‐5‐FU challenge. S<sc>tem</sc> C<sc>ells</sc><italic>2014;32:2550–2556</italic></p> </abstract>