| Literature DB >> 33071562 |
Xiaoting Wang1,2, Uddhab Karki1,2, Hasara Abeygunaratne2, Carmela UnnoldCofre2, Jianfeng Xu1,3.
Abstract
Ex vivo generation of red blood cells (RBCs) from hematopoietic stem cells (HSCs) used for blood transfusion represents one of the focuses in current regenerative medicine. However, massive production of HSCs-based RBCs requires a significant quantity of erythropoietic growth factors, making manufacturing at large scale cost prohibitive. Plant cell culture is proposed to be a promising bioproduction platform for functional human proteins in a safe and cost-efficient manner. This study exploited a proprietary technology, named HypGP engineering technology, for high-yield production of one of the key erythropoietic growth factors--stem cell factor (SCF)--in plant cell culture. Specifically, a designer hydroxyproline (Hyp)-O-glycosylated peptide (HypGP) comprised of 20 tandem repeats of the "Ser-Pro" motif, or (SP)20, was engineered at either the N-terminus or C-terminus of SCF in tobacco BY-2 cells. The (SP)20 tag dramatically increased the secreted yields of SCF up to 2.5 μg/ml. The (SP)20-tagged SCF showed bioactivity in promoting the proliferation of the TF-1 cell line, although the SCF-(SP)20 was 8.4-fold more potent than the (SP)20-SCF. Both the (SP)20-SCF and SCF-(SP)20 exhibited desired function in stimulating the expansion and differentiation of human umbilical cord blood CD34+ cells towards RBCs.Entities:
Keywords: Plant cell culture; hematopoietic stem cells; hydroxyproline-O-glycosylation; proliferation; stem cell factor
Year: 2020 PMID: 33071562 PMCID: PMC7561025 DOI: 10.1016/j.procbio.2020.09.029
Source DB: PubMed Journal: Process Biochem ISSN: 1359-5113 Impact factor: 3.757