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<p>Diseases affecting multiple peripheral nerves, termed polyneuropathies (PNPs), are common, mechanistically heterogeneous, and their causes are challenging to identify. Here, we integrated single-nucleus transcriptomics of peripheral nerves from 33 human PNP patients and four controls (365,708 nuclei) with subcellular spatial transcriptomics. We identified nerve cell type markers and uncovered unexpected heterogeneity of perineurial cells. PNPs shared a loss of myelinating and an increase in repair Schwann cells and endoneurial lipid-phagocytizing macrophages. Transcriptional changes affected multiple cells outside of the endoneurium across PNPs, suggesting PNPs as ‘pan-nerve diseases’. Spatially, PNPs—particularly those mediated by autoimmunity—exhibited focal perineurial hyperplasia and increased expression of <i>CXCL14</i>, identified as perineurial cell marker. Multi-omic characterization of human nerve biopsies thus identified novel mechanisms in PNPs with diagnostic potential.</p>

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Multi-omic identification of perineurial hyperplasia and lipid-associated nerve macrophages in human polyneuropathies

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月23日

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  • Michael Heming,
  • Anna-Lena Börsch,
  • Jolien Wolbert,
  • Christian Thomas,
  • Anne K. Mausberg,
  • Fabian Szepanowski,
  • Bianca Eggert,
  • I-Na Lu,
  • Julia Tietz,
  • Finja Dienhart,
  • Maja Meschnark,
  • Jan-Kolja Strecker,
  • Michael Glatza,
  • Carolina Thomas,
  • Noemi Gmahl,
  • Christine Dambietz,
  • Michael Müther,
  • Anne-Kathrin Uerschels,
  • Kathy Keyvani,
  • Jens Minnerup,
  • Kathrin Doppler,
  • Nurcan Üçeyler,
  • Julieta Aprea,
  • Andreas Dahl,
  • Ruth Stassart,
  • Robert Fledrich,
  • Heinz Wiendl,
  • Claudia Sommer,
  • Mark Stettner,
  • Gerd Meyer zu Hörste

摘要

Diseases affecting multiple peripheral nerves, termed polyneuropathies (PNPs), are common, mechanistically heterogeneous, and their causes are challenging to identify. Here, we integrated single-nucleus transcriptomics of peripheral nerves from 33 human PNP patients and four controls (365,708 nuclei) with subcellular spatial transcriptomics. We identified nerve cell type markers and uncovered unexpected heterogeneity of perineurial cells. PNPs shared a loss of myelinating and an increase in repair Schwann cells and endoneurial lipid-phagocytizing macrophages. Transcriptional changes affected multiple cells outside of the endoneurium across PNPs, suggesting PNPs as ‘pan-nerve diseases’. Spatially, PNPs—particularly those mediated by autoimmunity—exhibited focal perineurial hyperplasia and increased expression of CXCL14, identified as perineurial cell marker. Multi-omic characterization of human nerve biopsies thus identified novel mechanisms in PNPs with diagnostic potential.