Journal Article

Enhanced self-renewal of hematopoietic stem/progenitor cells mediated by the stem cell gene Sall4

Yang, Jianchang, Aguila, Jerell R, Ma, Yupo, Fink, Louis M, Alipio, Zaida, Lai, Raymond

2011

Overview

Background Sall4 is a key factor for the maintenance of pluripotency and self-renewal of embryonic stem cells (ESCs). Our previous studies have shown that Sall4 is a robust stimulator for human hematopoietic stem and progenitor cell (HSC/HPC) expansion. The purpose of the current study is to further evaluate how Sall4 may affect HSC/HPC activities in a murine system. Methods Lentiviral vectors expressing Sall4A or Sall4B isoform were used to transduce mouse bone marrow Lin-/Sca1+/c-Kit+ (LSK) cells and HSC/HPC self-renewal and differentiation were evaluated. Results Forced expression of Sall4 isoforms led to sustained ex vivo proliferation of LSK cells. In addition, Sall4 expanded HSC/HPCs exhibited increased in vivo repopulating abilities after bone marrow transplantation. These activities were associated with dramatic upregulation of multiple HSC/HPC regulatory genes including HoxB4, Notch1, Bmi1, Runx1, Meis1 and Nf-ya. Consistently, downregulation of endogenous Sall4 expression led to reduced LSK cell proliferation and accelerated cell differentiation. Moreover, in myeloid progenitor cells (32D), overexpression of Sall4 isoforms inhibited granulocytic differentiation and permitted expansion of undifferentiated cells with defined cytokines, consistent with the known functions of Sall4 in the ES cell system. Conclusion Sall4 is a potent regulator for HSC/HPC self-renewal, likely by increasing self-renewal activity and inhibiting differentiation. Our work provides further support that Sall4 manipulation may be a new model for expanding clinically transplantable stem cells.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Animals / Blood / Bone marrow / Bone Marrow Cells - metabolism / Cancer Research / Cell division / Cell growth / Cell Proliferation / Data collection / Differentiation / Disclosure / DNA-Binding Proteins - genetics / DNA-Binding Proteins - metabolism / Flow cytometry / Gene Expression Regulation - physiology / Genomics / Hematology / Hematopoietic stem cells / Hematopoietic Stem Cells - metabolism / Medicine / Medicine & Public Health / Mice / Mouse Hematopoietic Stem Cell / Oncology / Physiological aspects / Protein Isoforms / Proteins / Stem cells / Transcription Factors - genetics / Transcription Factors - metabolism / Transplantation