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Dysregulation of Cells Cycle and Apoptosis in Human Induced Pluripotent Stem Cells Chondrocytes Through p53 Pathway by HT-2 Toxin [Elektronisk resurs] An <em>in vitro</em> Study

Zhang, Yanan (författare)
Liu, Huan (författare)
Lin, Xialu (författare)
Zhang, Feng'e (författare)
Meng, Peilin (författare)
Tan, Sijia (författare)
Lammi, Mikko J., 1961- (författare)
Guo, Xiong (författare)
Chondrogenic and osteogenic differentiation (medarbetare)
Umeå universitet Medicinska fakulteten (utgivare)
Publicerad: Frontiers Media S.A. 2021
Engelska.
Ingår i: Frontiers in Genetics. - 1664-8021. ; 12
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  • Kashin–Beck disease (KBD) mainly damages growth plate of adolescents and is susceptible to both gene and gene–environmental risk factors. HT-2 toxin, which is a primary metabolite of T-2 toxin, was regarded as one of the environmental risk factors of KBD. We used successfully generated KBD human induced pluripotent stem cells (hiPSCs) and control hiPSCs, which carry different genetic information. They have potential significance in exploring the effects of HT-2 toxin on hiPSC chondrocytes and interactive genes with HT-2 toxin for the purpose of providing a cellular disease model for KBD. In this study, we gave HT-2 toxin treatment to differentiating hiPSC chondrocytes in order to investigate the different responses of KBD hiPSC chondrocytes and control hiPSC chondrocytes to HT-2 toxin. The morphology of HT-2 toxin-treated hiPSC chondrocytes investigated by transmission electron microscope clearly showed that the ultrastructure of organelles was damaged and type II collagen expression in hiPSC chondrocytes was downregulated by HT-2 treatment. Moreover, dysregulation of cell cycle was observed; and p53, p21, and CKD6 gene expressions were dysregulated in hiPSC chondrocytes after T-2 toxin treatment. Flow cytometry also demonstrated that there were significantly increased amounts of late apoptotic cells in KBD hiPSC chondrocytes and that the mRNA expression level of Fas was upregulated. In addition, KBD hiPSC chondrocytes presented stronger responses to HT-2 toxin than control hiPSC chondrocytes. These findings confirmed that HT-2 is an environmental risk factor of KBD and that p53 pathway interacted with HT-2 toxin, causing damaged ultrastructure of organelles, accelerating cell cycle in G1 phase, and increasing late apoptosis in KBD hiPSC chondrocytes. 

Ämnesord

Medical and Health Sciences  (hsv)
Basic Medicine  (hsv)
Cell and Molecular Biology  (hsv)
Medicin och hälsovetenskap  (hsv)
Medicinska och farmaceutiska grundvetenskaper  (hsv)
Cell- och molekylärbiologi  (hsv)
Clinical Medicine  (hsv)
Orthopaedics  (hsv)
Klinisk medicin  (hsv)
Ortopedi  (hsv)
Medical Biotechnology  (hsv)
Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)  (hsv)
Medicinsk bioteknologi  (hsv)
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)  (hsv)
cellforskning  (umu)
cell research  (umu)
Medical Cell Biology  (umu)
medicinsk cellbiologi  (umu)
Orthopaedics  (umu)
ortopedi  (umu)

Genre

government publication  (marcgt)

Indexterm och SAB-rubrik

HT-2 toxin
Kashin–Beck disease
cell apoptosis
cell cycle
p53
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Ingår i annan publikation. Gå till titeln Frontiers in Genetics

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