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. 2021 Nov 22;12(11):1840. doi: 10.3390/genes12111840

Figure 2.

Figure 2

The concept of mtDNA heteroplasmy and its contribution to mitochondrial dysfunction in PD. The arbitrary occurrence of mtDNA mutations (depicted by red-colored mitochondria) and their respective clonal expansion leads to different degrees of heteroplasmy in a given neuronal cell. Cell-specific heteroplasmy thresholds (dashed line) to cause mitochondrial dysfunction are widely unknown. By, e.g., shifting the degree of heteroplasmy towards a higher ratio of wildtype/mutated mtDNA, mitochondrial homeostasis might be restored. mtDNA: mitochondrial DNA.