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. 2026 Sep 28;17:1953711. doi: 10.3389/fimmu.2026.1953711

Table 1.

PBX1 metabolic functions across cell types.

Cell/tissue PBX1 context Metabolic pathway Mechanistic insight Functional consequence Disease/context Reference
Primitive erythroid cells Pbx1/Meis1 activity HIF1α signaling Meis1 induces Hif1a expression; Hif1α directly activates Gata1. Pbx1 cooperates with Meis1 upstream of erythroid specification Required for primitive erythropoiesis Hematopoiesis (97)
Mesangial cells PBX1 activity Glycolysis/lactate DNA immune complexes drive glycolysis/lactate-dependent PBX1 lactylation and degradation, reducing P27 expression and promoting G1–S transition Excessive mesangial cell proliferation Lupus nephritis (98)
Contralateral unaffected breast epithelium Increased PBX1 Lipid metabolism PBX1 promotes expression of lipid-metabolism genes. Altered lipid-metabolic transcriptional program ER-negative breast cancer (99)
Pancreatic cells Pbx1 deficiency Glucose homeostasis; insulin secretion PBX1 cooperates with Ipf1/Pdx1 to maintain pancreatic development and islet function Decreased insulin secretion; impaired glucose tolerance; diabetes susceptibility Diabetes mellitus (103)
Astrocytes PBX1 activity Glycolysis PBX1 represses Hk2, reducing L-serine synthesis Decreased glycolysis; accelerated astrocytic senescence; hyperglycemia and hyperinsulinemia Chronic stress (104)