TGFB1 is secreted through an unconventional pathway dependent on the autophagic machinery and cytoskeletal regulators

Autophagy. 2018;14(3):465-486. doi: 10.1080/15548627.2017.1422850. Epub 2018 Mar 11.

Abstract

TGFB1 (transforming growth factor beta 1) is a potent cytokine playing a driving role in development, fibrosis and cancer. It is synthesized as prodomain-growth factor complex that requires tethering to LTBP (latent transforming growth factor beta binding protein) for efficient secretion into the extracellular space. Upon release, this large latent complex is sequestered by anchorage to extracellular matrix (ECM) networks, from which the mature growth factor needs to be activated in order to reach its receptors and initiate signaling. Here, we uncovered a novel intracellular secretion pathway by which the latent TGFB1 complex reaches the plasma membrane and is released from fibroblasts, the key effector cells during tissue repair, fibrosis and in the tumor stroma. We show that secretion of latent TGFB1, but not of other selected cytokines or of bulk cargo, is regulated by fibroblast-ECM communication through ILK (integrin linked kinase) that restricts RHOA activity by interacting with ARHGAP26/GRAF1. Latent TGFB1 interacts with GORASP2/GRASP55 and is detected inside MAP1LC3-positive autophagosomal intermediates that are secreted by a RAB8A-dependent pathway. Interestingly, TGFB1 secretion is fully abrogated in human and murine fibroblasts and macrophages that lack key components of the autophagic machinery. Our data demonstrate an unconventional secretion mode of TGFB1 adding another level of control of its bioavailability and activity in order to effectively orchestrate cellular programs prone to dysregulation as seen in fibrosis and cancer.

Keywords: ARHGAP26/GRAF1; GORASP2/GRASP55; ILK; LIR motif; LTBP1; RAB8; RHOA; TNF; fibrosis; secretory autophagy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / physiology*
  • Biological Transport / physiology
  • Carrier Proteins / metabolism
  • Cells, Cultured
  • Cytoskeleton / metabolism*
  • Extracellular Matrix / metabolism
  • Fibroblasts / metabolism*
  • Fibrosis / metabolism
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mice
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • Carrier Proteins
  • Intracellular Signaling Peptides and Proteins
  • TGFB1 protein, human
  • Tgfb1 protein, mouse
  • Transforming Growth Factor beta1

Grants and funding

German Research Foundation [grant number SFB829], [grant number KR 558], [grant number RA 2838]; Imhoff Foundation; Koeln Fortune Program, Faculty of Medicine, Univ. of Cologne [grant number 216/2016].