Bioactive Materials (Jan 2022)

Programmable dual responsive system reconstructing nerve interaction with small-diameter tissue-engineered vascular grafts and inhibiting intimal hyperplasia in diabetes

  • Yanzhao Li,
  • Yeqin Wang,
  • Fangchao Xue,
  • Xuli Feng,
  • Zhaojing Ba,
  • Junjie Chen,
  • Zhenhua Zhou,
  • Yanhong Wang,
  • Ge Guan,
  • Guanyuan Yang,
  • Ziwei Xi,
  • Hao Tian,
  • Yong Liu,
  • Ju Tan,
  • Gang Li,
  • Xiewan Chen,
  • Mingcan Yang,
  • Wen Chen,
  • Chuhong Zhu,
  • Wen Zeng

Journal volume & issue
Vol. 7
pp. 466 – 477

Abstract

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Small-diameter tissue-engineered vascular grafts (sdTEVGs) with hyperglycemia resistance have not been constructed. The intimal hyperplasia caused by hyperglycemia remains problem to hinder the patency of sdTEVGs. Here, inspired by bionic regulation of nerve on vascular, we found the released neural exosomes could inhibit the abnormal phenotype transformation of vascular smooth muscle cells (VSMCs). The transformation was a prime culprit causing the intimal hyperplasia of sdTEVGs. To address this concern, sdTEVGs were modified with an on-demand programmable dual-responsive system of ultrathin hydrogels. An external primary Reactive Oxygen Species (ROS)-responsive Netrin-1 system was initially triggered by local inflammation to induce nerve remolding of the sdTEVGs overcoming the difficulty of nerve regeneration under hyperglycemia. Then, the internal secondary ATP-responsive DENND1A (guanine nucleotide exchange factor) system was turned on by the neurotransmitter ATP from the immigrated nerve fibers to stimulate effective release of neural exosomes. The results showed nerve fibers grow into the sdTEVGs in diabetic rats 30 days after transplantation. At day 90, the abnormal VSMCs phenotype was not detected in the sdTEVGs, which maintained long-time patency without intima hyperplasia. Our study provides new insights to construct vascular grafts resisting hyperglycemia damage.

Keywords