Homing and engraftment, a determining factor in hematopoietic stem cell transplantation success is defined as a process through which hematopoietic stem/progenitor cells (HSPCs) lodge recipient bone marrow. SDF-1/CXCR4 axis acts as a principle regulator in homing and engraftment, however, CXCR4 signaling is dependent upon expression of CXCR4 and its ligand SDF-1, which is highly dynamic. Hence, present investigation was aimed to explore the potential of CXCR4 constitutive active mutants (CXCR4-CAMs) in overcoming the limitation of CXCR4 signaling and up-modulate its efficiency in homing and engraftment. Regulated transgene expression study of these mutants revealed their significantly enhanced cell adhesion efficiency to endothelium and extracellular matrix protein. This altogether indicates promising prospects of CXCR4-CAMs in research aimed to improve HSPCs engraftment efficiency.
Keywords: Ala, Alanine; Asn, Asparagine; BM, Bone Marrow; BMEC, Bone marrow endothelial cells; BSA, Bovine Serum Albumin; CAMs, Constitutive Active Mutants; CXCR4; Conc., Concentration; ECM, Extracellular matrix; FBS, Fetal Bovine Serum; FN, Fibronectin; HSPCs; HSPCs, Hematopoietic Stem/ Progenitor Cells; HUVECs, Human Umbilical Vein Endothelial cells; IMDM, Iscove's Modified Dulbecco Media; LIF, Leukemia Inhibitory Factor; MCS, Multi Cloning Site; Ser, Serine; TM3, Transmembrane three domain; engraftment; homing.