[The extracellular domain of human delta-like-1 expressed and purified from CHO cells promotes expansion of hematopoietic progenitor cells]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2003 Jun;11(3):222-6.
[Article in Chinese]

Abstract

Notch signal path plays important roles in the regulation of proliferation and differentiation of hematopoietic stem cells. An extracellular domain of human Delta-like-1 (hDll-1(ext)), one of Notch ligands, was cloned and expressed in CHO cells, and the effect of hDll-1(ext) on expansion of hematopoietic stem/progenitor cells was investigated in this study. Total RNA was isolated from human marrow mononuclear cells. hDll-1(ext) was amplified by RT-PCR and cloned to T vector, then the gene was sequenced and subcloned to pcDNA3.1/Myc-His(+)A expression vector. The constructed plasmid was transfected into CHO cells with lipofectin and the expression of secreted hDll-1(ext) in G418-resistant clones was assayed by Western blot. hDll-1(ext) high-expressed clone was cultured to collect supernatant. Fusion protein hDll-1(ext) was purified from the supernatant by immobilized metal affinity chromatography (IMAC). The results showed that expression of Notch-1 receptor was detected in cord blood-derived CD34(+) cells by RT-PCR. Human umbilical blood CD34(+) cells were cultured in serum-free medium containing SCF, IL-3, VEGF, and with or without purified hDll-1(ext) for 4 or 8 days. Effect of hDll-1(ext) on the expansion of progenitor cells was analyzed then by clonogenic assays. The number of CFU-Mix and HPP-CFC generated from the culture system containing hDll-1(ext) was 1.5 times of that from the control. In conclusion, the recombinant hDll-1(ext) promotes the expansion of primitive hematopoietic progenitors.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD34 / immunology
  • Binding Sites / genetics
  • CHO Cells
  • Cell Division / drug effects
  • Cell Division / physiology
  • Colony-Forming Units Assay
  • Cricetinae
  • Endothelial Growth Factors / pharmacology
  • Fetal Blood / cytology
  • Fetal Blood / immunology
  • Fetal Blood / metabolism
  • Gene Expression
  • Genetic Vectors / genetics
  • Glycoproteins / genetics*
  • Glycoproteins / pharmacology
  • Glycoproteins / physiology
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Humans
  • Intercellular Signaling Peptides and Proteins / pharmacology
  • Interleukin-3 / pharmacology
  • Lymphokines / pharmacology
  • Membrane Proteins / genetics
  • RNA / genetics
  • RNA / metabolism
  • Receptor, Notch1
  • Receptors, Cell Surface*
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cell Factor / pharmacology
  • Transcription Factors*
  • Transfection
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Antigens, CD34
  • Endothelial Growth Factors
  • Glycoproteins
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-3
  • Lymphokines
  • Membrane Proteins
  • NOTCH1 protein, human
  • Receptor, Notch1
  • Receptors, Cell Surface
  • Recombinant Proteins
  • Stem Cell Factor
  • Transcription Factors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • RNA