Spatiotemporal activation of Rac1 for engulfment of apoptotic cells

  1. Michio Nakaya*,,,
  2. Masahiro Kitano§,
  3. Michiyuki Matsuda§, and
  4. Shigekazu Nagata*,,
  1. Departments of *Medical Chemistry and
  2. §Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University, Yoshida Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan; and
  3. Solution Oriented Research for Science and Technology, Japan Science and Technology Corporation, Yoshida Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan
  1. Communicated by Yoshito Kaziro, Kyoto University, Kyoto, Japan, April 22, 2008 (received for review December 6, 2007)

Abstract

The engulfment of apoptotic cells requires phagocytes to coordinately activate Rho family GTPases that regulate actin dynamics. Here, we used a FRET biosensor to visualize the spatiotemporal activation of Rac1 during engulfment of apoptotic cells. We report that apoptotic cells were usually engulfed by the phagocytes' lamellipodia, where Rac1 was activated. Often, apoptotic cells were engulfed successively at the same lamellipodial site, suggesting the presence of portals for apoptotic cells. At this location, the activated Rac1 was recruited to form phagocytic cups that were comprised of actin patches. When the phagocytic cup was closed, Rac1 was down-regulated, and the actin patches were abruptly broken down. The constitutively active Rac1 remained at phagocytic cup for a longer period than the wild-type Rac1, and the closure of the phagocytic cup was significantly delayed in cells expressing a constitutive active form of Rac1, resulting in inefficient engulfment. These results indicate that activated Rac1 is necessary to assemble F-actin, but closing the phagocytic cup requires Rac1 to be deactivated.

Footnotes

  • To whom correspondence should be sent at the * address. E-mail: snagata{at}mfour.med.kyoto-u.ac.jp
  • Author contributions: M.N., M.M., and S.N. designed research; M.N. and M.K. performed research; M.N., M.K., and S.N. analyzed data; and M.N. and S.N. wrote the paper.

  • Present address: Department of Pharmacology and Toxicology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812–8582, Japan.

  • The authors declare no conflict of interest.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0803677105/DCSupplemental.

  • Freely available online through the PNAS open access option.

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