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Mitochondrial (mt) DNA can be classified into haplogroups, which represent populations with different geographic origins. Individuals of maternal African backgrounds (L haplogroup) are more prone to develop specific diseases compared those with maternal European-H haplogroups. Using a cybrid model, effects of amyloid-β (Amyβ), sub-lethal ultraviolet (UV) radiation, and 5-Aza-2′-deoxycytidine (5-aza-dC), a methylation inhibitor, were investigated. Amyβ treatment decreased cell metabolism and increased levels of reactive oxygen species in European-H and African-L cybrids, but lower mitochondrial membrane potential (ΔΨM) was found only in African-L cybrids. Sub-lethal UV radiation induced higher expression levels of <i>CFH</i>, <i>EFEMP1</i>, <i>BBC3</i>, and <i>BCL2L13</i> in European-H cybrids compared to African-L cybrids. With respect to epigenetic status, the African-L cybrids had (<b>a</b>) 4.7-fold higher total global methylation levels (<i>p</i> = 0.005); (<b>b</b>) lower expression patterns for <i>DNMT3B</i>; and (<b>c</b>) elevated levels for <i>HIST1H3F</i>. The European-H and African-L cybrids showed different transcription levels for <i>CFH</i>, <i>EFEMP1</i>, <i>CXCL1</i>, <i>CXCL8</i>, <i>USP25</i>, and <i>VEGF</i> after treatment with 5-aza-dC. In conclusion, compared to European-H haplogroup cybrids, the African-L cybrids have different (<b>i</b>) responses to exogenous stressors (Amyβ and UV radiation), (<b>ii</b>) epigenetic status, and (<b>iii</b>) modulation profiles of methylation-mediated downstream complement, inflammation, and angiogenesis genes, commonly associated with various human diseases.