Cells (Jul 2020)

Mertk Interacts with Tim-4 to Enhance Tim-4-Mediated Efferocytosis

  • Byeongjin Moon,
  • Juyeon Lee,
  • Sang-Ah Lee,
  • Chanhyuk Min,
  • Hyunji Moon,
  • Deokhwan Kim,
  • Susumin Yang,
  • Heera Moon,
  • Jaeseon Jeon,
  • Young-Eun Joo,
  • Daeho Park

DOI
https://doi.org/10.3390/cells9071625
Journal volume & issue
Vol. 9, no. 7
p. 1625

Abstract

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Apoptotic cells expressing phosphatidylserine (PS) on their cell surface are directly or indirectly recognized by phagocytes through PS-binding proteins. The PS-binding protein Tim-4 secures apoptotic cells to phagocytes to facilitate the engulfment of apoptotic cells. However, the molecular mechanism by which Tim-4 transduces signals to phagocytes during Tim-4-mediated efferocytosis is incompletely understood. Here, we report that Tim-4 collaborates with Mertk during efferocytosis through a biochemical interaction with Mertk. Proximal localization between the two proteins in phagocytes was observed by immunofluorescence and proximal ligation assays. Physical association between Tim-4 and Mertk, which was mediated by an interaction between the IgV domain of Tim-4 and the fibronectin type-III domain of Mertk, was also detected with immunoprecipitation. Furthermore, the effect of Mertk on Tim-4-mediated efferocytosis was abolished by GST-MertkFnIII, a soluble form of the fibronectin type-III domain of Mertk that disrupts the interaction between Tim-4 and Mertk. Taken together, the results from our study suggest that a physical interaction between Tim-4 and Mertk is necessary for Mertk to enhance efferocytosis mediated by Tim-4.

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