The nucleoside diphosphate kinase NDK‐1/NME1 promotes phagocytosis in concert with DYN‐1/Dynamin. Issue 10 (17th July 2019)
- Record Type:
- Journal Article
- Title:
- The nucleoside diphosphate kinase NDK‐1/NME1 promotes phagocytosis in concert with DYN‐1/Dynamin. Issue 10 (17th July 2019)
- Main Title:
- The nucleoside diphosphate kinase NDK‐1/NME1 promotes phagocytosis in concert with DYN‐1/Dynamin
- Authors:
- Farkas, Zsolt
Petric, Metka
Liu, Xianghua
Herit, Floriane
Rajnavölgyi, Éva
Szondy, Zsuzsa
Budai, Zsófia
Orbán, Tamás I.
Sándor, Sára
Mehta, Anil
Bajtay, Zsuzsa
Kovács, Tibor
Jung, Sung Yun
Shakir, Muhammed Afaq
Qin, Jun
Zhou, Zheng
Niedergang, Florence
Boissan, Mathieu
Takács-Vellai, Krisztina - Abstract:
- ABSTRACT: Phagocytosis of various targets, such as apoptotic cells or opsonized pathogens, by macrophages is coordinated by a complex signaling network initiated by distinct phagocytic receptors. Despite the different initial signaling pathways, each pathway ends up regulating the actin cytoskeletal network, phagosome formation and closure, and phagosome maturation leading to degradation of the engulfed particle. Herein, we describe a new phagocytic function for the nucleoside diphosphate kinase 1 (NDK‐1), the nematode counterpart of the first identified metastasis inhibitor NM23‐H1 (nonmetastatic clone number 23) nonmetastatic clone number 23 or nonmetastatic isoform 1 (NME1). We reveal by coimmunoprecipitation, Duolink proximity ligation assay, and mass spectrometry that NDK‐1/NME1 works in a complex with DYN‐1/Dynamin ( Caenorhabditis elegans /human homolog proteins), which is essential for engulf ment and phagosome maturation. Time‐lapse microscopy shows that NDK‐1 is expressed on phagosomal surfaces during cell corpse clearance in the same time window as DYN‐1. Silencing of NM23‐M1 in mouse bone marrow—derived macrophages resulted in decreased phagocytosis of apoptotic thymocytes. In human macrophages, NM23‐H1 and Dynamin are corecruited at sites of phagosome formation in F‐actin—rich cups. In addition, NM23‐H1 was required for efficient phagocytosis. Together, our data demonstrate that NDK‐1/NME1 is an evolutionarily conserved element of successfulABSTRACT: Phagocytosis of various targets, such as apoptotic cells or opsonized pathogens, by macrophages is coordinated by a complex signaling network initiated by distinct phagocytic receptors. Despite the different initial signaling pathways, each pathway ends up regulating the actin cytoskeletal network, phagosome formation and closure, and phagosome maturation leading to degradation of the engulfed particle. Herein, we describe a new phagocytic function for the nucleoside diphosphate kinase 1 (NDK‐1), the nematode counterpart of the first identified metastasis inhibitor NM23‐H1 (nonmetastatic clone number 23) nonmetastatic clone number 23 or nonmetastatic isoform 1 (NME1). We reveal by coimmunoprecipitation, Duolink proximity ligation assay, and mass spectrometry that NDK‐1/NME1 works in a complex with DYN‐1/Dynamin ( Caenorhabditis elegans /human homolog proteins), which is essential for engulf ment and phagosome maturation. Time‐lapse microscopy shows that NDK‐1 is expressed on phagosomal surfaces during cell corpse clearance in the same time window as DYN‐1. Silencing of NM23‐M1 in mouse bone marrow—derived macrophages resulted in decreased phagocytosis of apoptotic thymocytes. In human macrophages, NM23‐H1 and Dynamin are corecruited at sites of phagosome formation in F‐actin—rich cups. In addition, NM23‐H1 was required for efficient phagocytosis. Together, our data demonstrate that NDK‐1/NME1 is an evolutionarily conserved element of successful phagocytosis.—Farkas, Z., Petric, M., Liu, X., Herit, F., Rajnavölgyi, É., Szondy, Z., Budai, Z., Orbán, T. I., Sándor, S., Mehta, A., Bajtay, Z., Kovács, T., Jung, S. Y., Afaq Shakir, M., Qin, J., Zhou, Z., Niedergang, F., Boissan, M., Takács‐Vellai, K. The nucleoside diphosphate kinase NDK‐1/NME1 promotes phagocytosis in concert with DYN‐1/dynamin. FASEB J. 33, 11606–11614 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 10(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 10(2019)
- Issue Display:
- Volume 33, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 10
- Issue Sort Value:
- 2019-0033-0010-0000
- Page Start:
- 11606
- Page End:
- 11614
- Publication Date:
- 2019-07-17
- Subjects:
- metastasis inhibitor -- apoptotic clearance -- phagosome formation -- phagosome maturation -- actin cup
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201900220R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13234.xml