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Published on: April 12, 2015
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.).
Abstract:
Megakaryocytes (MKs) are rare polyploid cells found in the bone marrow and produce platelets. Platelets are small cell fragments that are essential during wound healing and vascular hemostasis. In vitro differentiation of MKs from human-induced pluripotent stem cell-derived CD34+ hematopoietic stem cells (hiPSC-HSCs) could provide an alternative treatment option for thrombocytopenic patients as a platelet source. In this approach, we developed a method to produce functional MKs from hiPSC-HSCs using a xeno-free and feeder-free condition and minimize the variation and risk from animal-derived products in cell culture. We have also investigated the genome-wide expression as well as functional significance of long noncoding RNAs (lncRNAs) in hiPSC-HSC-derived MKs to get insight into MK biology. We have performed lncRNAs expression profiling by using the Human LncProfilers qPCR Array Kit and identified 26 differentially regulated lncRNAs in hiPSC-HSC-derived MKs as compared with those in hiPSC-HSCs. HOX antisense intergenic RNA myeloid 1 (HOTAIRM1) was the most highly upregulated lncRNA in hiPSC-HSC-derived MKs and phorbol 12-myristate 13-acetate (PMA)-induced megakaryocytic-differentiating K562 cells. Furthermore, we have studied the potential mechanism of HOTAIRM1 based on the interactions between HOTAIRM1, p53, and miR-125b in PMA-induced K562 cells. Our results demonstrated that during MK maturation, HOTAIRM1 might be associated with the transcriptional regulation of p53 via acting as a decoy for miR-125b. Thus, the interaction between HOTAIRM1, p53, and miR-125b is likely involved in controlling cell cycling (cyclin D1), reactive oxygen species production, and apoptosis to support terminal maturation of MKs. SIGNIFICANCE STATEMENT: In vitro generation of megakaryocytes (MKs) from human-induced pluripotent stem cell-derived hematopoietic stem cells (hiPSC-HSCs) could provide an alternative source of platelets for treating thrombocytopenic patients. This study has investigated the functional significance of long non-coding RNAs in hiPSC-HSC-derived MKs, which remains unclear. This study's findings suggest that the regulatory role of HOX antisense intergenic RNA myeloid 1 (HOTAIRM1) in p53-mediated regulation of cyclin D1 during megakaryocytopoiesis is to promote MK maturation by decoying miR-125b.
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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