Single-nucleus RNA-Seq reveals singular gene signatures of human ductal cells during adaptation to insulin resistance

JCI Insight. 2022 Aug 22;7(16):e153877. doi: 10.1172/jci.insight.153877.

Abstract

Adaptation to increased insulin demand is mediated by β cell proliferation and neogenesis, among other mechanisms. Although it is known that pancreatic β cells can arise from ductal progenitors, these observations have been limited mostly to the neonatal period. We have recently reported that the duct is a source of insulin-secreting cells in adult insulin-resistant states. To further explore the signaling pathways underlying the dynamic β cell reserve during insulin resistance, we undertook human islet and duct transplantations under the kidney capsule of immunodeficient NOD/SCID-γ (NSG) mouse models that were pregnant, were insulin-resistant, or had insulin resistance superimposed upon pregnancy (insulin resistance + pregnancy), followed by single-nucleus RNA-Seq (snRNA-Seq) on snap-frozen graft samples. We observed an upregulation of proliferation markers (e.g., NEAT1) and expression of islet endocrine cell markers (e.g., GCG and PPY), as well as mature β cell markers (e.g., INS), in transplanted human duct grafts in response to high insulin demand. We also noted downregulation of ductal cell identity genes (e.g., KRT19 and ONECUT2) coupled with upregulation of β cell development and insulin signaling pathways. These results indicate that subsets of ductal cells are able to gain β cell identity and reflect a form of compensation during the adaptation to insulin resistance in both physiological and pathological states.

Keywords: Beta cells; Development; Endocrinology; Islet cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Animals
  • Female
  • Homeodomain Proteins
  • Humans
  • Infant, Newborn
  • Insulin / metabolism
  • Insulin Resistance* / genetics
  • Mice
  • Mice, Inbred NOD
  • Mice, Nude
  • Mice, SCID
  • Pregnancy
  • RNA-Seq
  • Transcription Factors

Substances

  • Homeodomain Proteins
  • Insulin
  • ONECUT2 protein, human
  • Transcription Factors