Selective knockdown of hexokinase 2 in rods leads to age-related photoreceptor degeneration and retinal metabolic remodeling

• Published in: Cell death & disease Vol. 11; no. 10; p. 885
• Main Authors: Zhang, Rui, Shen, Weiyong, Du, Jianhai, Gillies, Mark C.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.10.2020; Springer Nature B.V
• Subjects: 101/58; 13/51; 14/19; 631/378/340; 64/110; 692/699/375; 82/80; Age; Age Factors; Animals; Antibodies; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Culture; Citric Acid Cycle - physiology; Enzymes; Glucose; Glycolysis; Hexokinase; Hexokinase - genetics; Hexokinase - metabolism; Immunohistochemistry; Immunology; Life Sciences; Mass spectrometry; Mass spectroscopy; Metabolism; Metabolites; Mice, Transgenic; Mitochondria; Mitochondria - metabolism; Mitochondrial Proteins - metabolism; Oxidative phosphorylation; Phosphorylation; Photoreceptors; Phototransduction; Proteins; Pyruvate kinase; Pyruvic acid; Retina; Retina - metabolism; Retinal degeneration; Retinal Degeneration - metabolism; Retinal Rod Photoreceptor Cells - metabolism; Rhodopsin; Rods; Scientific imaging; Stress proteins; Structure-function relationships; Tomography, Optical Coherence - methods; Tricarboxylic acid cycle; Western blotting
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-020-03103-7

Photoreceptors, the primary site of phototransduction in the retina, require energy and metabolites to constantly renew their outer segments. They preferentially consume most glucose through aerobic glycolysis despite possessing abundant mitochondria and enzymes for oxidative phosphorylation (OXPHOS). Exactly how photoreceptors balance aerobic glycolysis and mitochondrial OXPHOS to regulate their survival is still unclear. We crossed rhodopsin-Cre mice with hexokinase 2 (HK2)-floxed mice to study the effect of knocking down HK2, the first rate-limiting enzyme in glycolysis, on retinal health and metabolic remodeling. Immunohistochemistry and Western blots were performed to study changes in photoreceptor-specific proteins and key enzymes in glycolysis and the tricarboxylic acid (TCA) cycle. Changes in retinal structure and function were studied by optical coherence tomography and electroretinography. Mass spectrometry was performed to profile changes in 13 C-glucose-derived metabolites in glycolysis and the TCA cycle. We found that knocking down HK2 in rods led to age-related photoreceptor degeneration, evidenced by reduced expression of photoreceptor-specific proteins, age-related reductions of the outer nuclear layer, photoreceptor inner and outer segments and impaired electroretinographic responses. Loss of HK2 in rods led to upregulation of HK1, phosphorylation of pyruvate kinase muscle isozyme 2, mitochondrial stress proteins and enzymes in the TCA cycle. Mass spectrometry found that the deletion of HK2 in rods resulted in accumulation of 13 C-glucose along with decreased pyruvate and increased metabolites in the TCA cycle. Our data suggest that HK2-mediated aerobic glycolysis is indispensable for the maintenance of photoreceptor structure and function and that long-term inhibition of glycolysis leads to photoreceptor degeneration.