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However, using a proteomic approach on a subset of placental samples, numerous mitochondrial proteins were found to be down-regulated in PE3 placentas compared with controls, including: subunits of OXPHOS protein complexes (NADH:Ubiquinone Oxidoreductase Subunit V3 [NDUFV3], Ubiquinol-Cytochrome C Reductase Core Protein 1 [UQCRC1], and UQCR Rieske Iron-Sulfur Polypeptide 1[UQCRFS1]), and proteins that affect mitochondrial dynamics (optic atrophy type 1 [OPA1]), mitochondrial import (TOMM7), and mitochondrial translation (mitochondrial ribosomal proteins, MRPS36, MRPL44, MRPS36, MRPL22, MRPL1), among others (Fig 1H)
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Whether they gave the peptide body-wide or delivered it directly to the kidneys, it reduced the movement of immune cells into the kidneys, resolved inflammation and damage and improved kidney function, without increasing blood pressure, they report in the journal Kidney International
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