Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1.

Abstract

Dyskeratosis congenita (DC) is a rare telomere biology disorder, which results in different clinical manifestations, including severe bone marrow failure. To date, the only curative treatment for the bone marrow failure in DC patients is allogeneic hematopoietic stem cell transplantation. However, due to the toxicity associated to this treatment, improved therapies are recommended for DC patients. Here, we aimed at generating DC-like human hematopoietic stem cells in which the efficacy of innovative therapies could be investigated. Because X-linked DC is the most frequent form of the disease and is associated with an impaired expression of DKC1, we have generated DC-like hematopoietic stem cells based on the stable knock-down of DKC1 in human CD34+ cells with lentiviral vectors encoding for DKC1 short hairpin RNAs. At a molecular level, DKC1-interfered CD34+ cells showed a decreased expression of TERC, as well as a diminished telomerase activity and increased DNA damage, cell senescence, and apoptosis. Moreover, DKC1-interfered human CD34+ cells showed defective clonogenic ability and were incapable of repopulating the hematopoiesis of immunodeficient NSG mice. The development of DC-like hematopoietic stem cells will facilitate the understanding of the molecular and cellular basis of this inherited bone marrow failure syndrome and will serve as a platform to evaluate the efficacy of new hematopoietic therapies for DC.

• Authors: Carlos Carrascoso-Rubio, Hidde A Zittersteijn, Laura Pintado-Berninches, Beatriz Fernández-Varas, M Luz Lozano, Cristina Manguan-Garcia, Leandro Sastre, Juan A Bueren, Rosario Perona, Guillermo Guenechea
• Journal: Stem cell research & therapy (Stem Cell Res Ther) Vol. 12 Issue 1 Pg. 92 (01 29 2021) ISSN: 1757-6512 [Electronic] England
• PMID: 33514435 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Cell Cycle Proteins
• DKC1 protein, human
• Nuclear Proteins
• Telomerase

Topics

• Animals
• Cell Cycle Proteins (genetics)
• Dyskeratosis Congenita (genetics, therapy)
• Hematopoietic Stem Cells (metabolism)
• Humans
• Mice
• Mutation
• Nuclear Proteins (genetics)
• Telomerase (genetics, metabolism)
• Telomere (metabolism)