We focus on two major types of disease models in our group:

1. 2D/3D muscle disease models
The muscle stem cells or myoblasts are the valuable source to model muscle diseases due to their remarkable ability to regenerate new myofibers. The primary muscle cells are significantly limited in applications by their inability to expand in culture for long term. The immortalized myoblasts or iPSCs are becoming alternative, in particular the patient-derived iPSCs due to its characteristics such as immortality, multi-lineage differentiation potential to 3D muscles, and patient genomic specificity. The CRIPSR tools can either be used to correct mutations in the disease models or generate mutation carrying cell lines to model muscle diseases.

Figure 3: The muscle disease phenotype and cells used for modeling muscles. (A) The muscle biopsy from patient with centronuclear myopathy (Wang et al., 2018). (B) The iPSCs derived from a muscular dystrophy patient (Wang et al., 2022). (C) Myotubes via differentiation of human muscle stem cells (D) Myotubes via differentiation of immortalized mouse myoblast cell line C2C12. (E) Scheme of a cytosine base editing in iPSCs either for correction or introduction of mutations (modified from Wang et al., 2022).

Project: CNMuscle, funded by ZNM - Zusammen Stark! e.V.

Duration: 01.11.2023 - 30.04.2026
More information can be found here.

 

2. 2D Neuronal disease models 
For the NMDs affecting the nerves or brain, the in vitro neuronal model allows the systematic evaluation of the mutated neuronal receptors or transporters, further providing a genotype-phenotype correlation or suggesting treatment strategies. 

Figure 2: The neuronal disease phenotypes and neuronal cell lines used for modeling neurons. (A) The sural nerve biopsy from patient with neuropathy (Wang et al., 2018). (B) The MRI scan of patient with brain atrophy (Wang et al., 2017). (C) The undifferentiated rat PC12 cells transiently expressing neuronal transporter CHT encoded by SLC5A7 gene (Wang et al., 2017). (D) A neuron network from differentiated human neuroblastoma cell line SH-SY5Y.

If you are interested in our disease cell models, please contact us and we are glad to collaborate. Students and scientists are also welcome to join our team.

Selected References

  1. Wang H#, Krause A, Escobar H, Müthel S, Metzler E, Spuler S#. LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction. International Journal of Molecular Sciences 2022; 23 (24), 15525. (Co-corresponding authors).
  2. Wang H, Kaçar Bayram A, Sprute R, Ozdemir O, Cooper E, Pergande M, ..., Cirak S. Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking. Frontiers in Neuroscience 2019; 13, 974.
  3. Wang H*, Schänzer A*, Kampschulte B, Daimagüler HS, Logeswaran T, Schlierbach H, ..., Cirak S. A novel SPEG mutation causes non-compaction cardiomyopathy and neuropathy in a floppy infant with centronuclear myopathy. Acta Neuropathologica Communications 2018; 6 (1), 1-5. (Co-first authors)
  4. Wang H*, Salter CG*, Refai O*, Hardy H, Barwick KES, Akpulat U, ..., Crosby AH. Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization. Brain 2017; 140 (11), 2838-2850. (Co-first authors)
  5. Baarlink C, Wang H, Grosse R. Nuclear actin network assembly by formins regulates the SRF coactivator MAL. Science 2013; 340 (6134), 864-867.

Dr. Haicui Wang

Group leader