Role of Long Non-Coding RNAs in Human-Induced Pluripotent Stem Cells Derived Megakaryocytes: A p53, HOX Antisense

Swati Dahariya1, Sanjeev Raghuwanshi1, Vasanth Thamodaran1

  • 1Stem Cell Research Laboratory, Department of Biochemistry, School of Life Sciences, University of Hyderabad, Hyderabad, India (S.D., S.R., R.K.G.) and Centre for Stem Cell Research, Christian Medical College, Vellore, India (V.T., S.R.V.).

Insights

Generating functional megakaryocytes (MKs) from human-induced pluripotent stem cells (hiPSC-HSCs) offers a potential platelet source for patients with thrombocytopenia. This study reveals that the long noncoding RNA HOTAIRM1 promotes MK maturation by regulating p53 and cyclin D1 via miR-125b decoy activity.

Area of Science:

  • Stem cell biology
  • Hematopoiesis
  • Molecular genetics

Background:

  • Megakaryocytes (MKs) are crucial for platelet production, essential for hemostasis and wound healing.
  • In vitro generation of MKs from human-induced pluripotent stem cell-derived hematopoietic stem cells (hiPSC-HSCs) presents a therapeutic avenue for thrombocytopenic patients.
  • The role of long noncoding RNAs (lncRNAs) in MK differentiation remains largely unexplored.

Purpose of the Study:

  • To develop a xeno-free, feeder-free method for producing functional MKs from hiPSC-HSCs.
  • To investigate the genome-wide expression and functional significance of lncRNAs during hiPSC-HSC-derived MK differentiation.
  • To elucidate the mechanism of HOTAIRM1 in regulating MK maturation.

Main Methods:

  • Differentiation of hiPSC-HSCs into MKs under xeno-free, feeder-free conditions.
  • lncRNA expression profiling using Human LncProfilers qPCR Array Kit.
  • Mechanistic studies involving HOTAIRM1, p53, and miR-125b in PMA-induced K562 cells.

Main Results:

  • A robust method for generating functional MKs from hiPSC-HSCs was established.
  • 26 differentially regulated lncRNAs were identified, with HOTAIRM1 being significantly upregulated during MK maturation.
  • HOTAIRM1 acts as a decoy for miR-125b, potentially regulating p53 transcriptional activity and influencing cell cycling, ROS production, and apoptosis to promote MK terminal differentiation.

Conclusions:

  • Xeno-free, feeder-free in vitro generation of MKs from hiPSC-HSCs is feasible and offers a promising source of platelets.
  • HOTAIRM1 plays a critical role in MK maturation by modulating the HOTAIRM1-miR-125b-p53 axis.
  • This regulatory network involving HOTAIRM1, p53, and miR-125b is implicated in controlling key cellular processes that support megakaryocytopoiesis.

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