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A plant-derived natural photosynthetic system for improving cell anabolism.

Pengfei ChenXin LiuChenhui GuPeiyu ZhongNan SongMobai LiZhanqiu DaiXiangqian FangZaiqiang MaJianfeng ZhangRuikang TangShunwu FanXianfeng Lin
Published in: Nature (2022)
Insufficient intracellular anabolism is a crucial factor involved in many pathological processes in the body 1,2 . The anabolism of intracellular substances requires the consumption of sufficient intracellular energy and the production of reducing equivalents. ATP acts as an 'energy currency' for biological processes in cells 3,4 , and the reduced form of NADPH is a key electron donor that provides reducing power for anabolism 5 . Under pathological conditions, it is difficult to correct impaired anabolism and to increase insufficient levels of ATP and NADPH to optimum concentrations 1,4,6-8 . Here we develop an independent and controllable nanosized plant-derived photosynthetic system based on nanothylakoid units (NTUs). To enable cross-species applications, we use a specific mature cell membrane (the chondrocyte membrane (CM)) for camouflage encapsulation. As proof of concept, we demonstrate that these CM-NTUs enter chondrocytes through membrane fusion, avoid lysosome degradation and achieve rapid penetration. Moreover, the CM-NTUs increase intracellular ATP and NADPH levels in situ following exposure to light and improve anabolism in degenerated chondrocytes. They can also systemically correct energy imbalance and restore cellular metabolism to improve cartilage homeostasis and protect against pathological progression of osteoarthritis. Our therapeutic strategy for degenerative diseases is based on a natural photosynthetic system that can controllably enhance cell anabolism by independently providing key energy and metabolic carriers. This study also provides an enhanced understanding of the preparation and application of bioorganisms and composite biomaterials for the treatment of disease.
Keyphrases
  • reactive oxygen species
  • single cell
  • extracellular matrix
  • induced apoptosis
  • cell cycle arrest
  • molecularly imprinted
  • replacement therapy
  • single molecule
  • loop mediated isothermal amplification
  • electron transfer