Iroquois Homeobox Protein 2 Identified as a Potential Biomarker for Parkinson's Disease.
Hyuna SimJoo-Eun LeeHee Min YooSunwha ChoHana LeeAruem BaekJisun KimHyemyung SeoMi-Na KweonHyung Gun KimYoung-Joo JeonMyung Jin SonJanghwan KimPublished in: International journal of molecular sciences (2020)
The diagnosis of Parkinson's disease (PD) is initiated after the occurrence of motor symptoms, such as resting tremors, rigidity, and bradykinesia. According to previous reports, non-motor symptoms, notably gastrointestinal dysfunction, could potentially be early biomarkers in PD patients as such symptoms occur earlier than motor symptoms. However, connecting PD to the intestine is methodologically challenging. Thus, we generated in vitro human intestinal organoids from PD patients and ex vivo mouse small intestinal organoids from aged transgenic mice. Both intestinal organoids (IOs) contained the human LRRK2 G2019S mutation, which is the most frequent genetic cause of familial and sporadic PD. By conducting comprehensive genomic comparisons with these two types of IOs, we determined that a particular gene, namely, Iroquois homeobox protein 2 (IRX2), showed PD-related expression patterns not only in human pluripotent stem cell (PSC)-derived neuroectodermal spheres but also in human PSC-derived neuronal cells containing dopaminergic neurons. We expected that our approach of using various cell types presented a novel technical method for studying the effects of multi-organs in PD pathophysiology as well as for the development of diagnostic markers for PD.
Keyphrases
- endothelial cells
- induced pluripotent stem cells
- end stage renal disease
- stem cells
- newly diagnosed
- pluripotent stem cells
- ejection fraction
- chronic kidney disease
- poor prognosis
- spinal cord
- sleep quality
- peritoneal dialysis
- oxidative stress
- copy number
- single cell
- heart rate
- early onset
- mesenchymal stem cells
- induced apoptosis
- cell death
- spinal cord injury
- prognostic factors
- depressive symptoms
- signaling pathway
- late onset
- brain injury