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The two peptides operate through largely complementary rather than overlapping mechanisms, which suggests a potentially additive or even synergistic effect in tissue repair models

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Erastin-activated ferroptosis was found to increase the levels of lysosome-associated membrane protein 2a, also known as CD107b, to promote chaperone-mediated autophagy (CMA), which in turn, promotes the degradation of GPX4

However, a logical biochemical explanation has been proposed by Pendergrass and Haley, based on the different amino-acid configurations of the three apo-E isomers and their potential relevance to mercury elimination