Phagocytosis: Elegant complexity

被引:515
作者
Stuart, LM
Ezekowitz, RAB [1 ]
机构
[1] Massachusetts Gen Hosp, Lab Dev Immunol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
[3] Univ Edinburgh, Ctr Inflammat Res, Edinburgh EH8 9AG, Midlothian, Scotland
关键词
D O I
10.1016/j.immuni.2005.05.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phagocytosis requires receptor-mediated recognition of particles, usually in the guise of infectious agents and apoptotic cells. Phagosomes fuse with lysosomes to generate phagolysosomes, which play a key role in enzymatic digestion of the internalized contents into component parts. Recent findings indicate that a simple paradigm of a single cognate receptor interaction that guides the phagosome to phagolysosome formation belles the complexity of combinatorial receptor recognition and diversity of phagosome function. In fact, phagosomes are comprised of hundreds of proteins that play a key role in deciphering the contents of the phagosome and in defining host response. In this review we discuss how the challenge of recognizing diverse molecular patterns is met by combinatorial interactions between phagocytic receptors. Furthermore, these combinations are dynamic and both sculpt the balance between a proinflammatory or anti-inflammatory response and direct phagosome diversity. We also indicate an important role for genetically tractable model organisms in defining key components of this evolutionarily conserved process.
引用
收藏
页码:539 / 550
页数:12
相关论文
共 95 条
[1]   Access of soluble antigens to the endoplasmic reticulum can explain cross-presentation by dendritic cells [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
NATURE IMMUNOLOGY, 2005, 6 (01) :107-113
[2]   Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12889-12894
[3]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[4]   LIGATED COMPLEMENT RECEPTORS DO NOT ACTIVATE THE ARACHIDONIC-ACID CASCADE IN RESIDENT PERITONEAL-MACROPHAGES [J].
ADEREM, AA ;
WRIGHT, SD ;
SILVERSTEIN, SC ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (03) :617-622
[5]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[6]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[7]   Serum-derived protein S binds to phosphatidylserine and stimulates the phagocytosis of apoptotic cells [J].
Anderson, HA ;
Maylock, CA ;
Williams, JA ;
Paweletz, CP ;
Shu, HJ ;
Shacter, E .
NATURE IMMUNOLOGY, 2003, 4 (01) :87-91
[8]   PHAGOSOME-LYSOSOME INTERACTIONS IN CULTURED MACROPHAGES INFECTED WITH VIRULENT TUBERCLE-BACILLI - REVERSAL OF USUAL NONFUSION PATTERN AND OBSERVATIONS ON BACTERIAL SURVIVAL [J].
ARMSTRONG, JA ;
HART, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 142 (01) :1-16
[9]   Focal exocytosis of VAMP3-containing vesicles at sites of phagosome formation [J].
Bajno, L ;
Peng, XR ;
Schreiber, AD ;
Moore, HP ;
Trimble, WS ;
Grinstein, S .
JOURNAL OF CELL BIOLOGY, 2000, 149 (03) :697-705
[10]   Differential use of endoplasmic reticulum membrane for phagocytosis in J774 macrophages [J].
Becker, T ;
Volchuk, A ;
Rothman, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (11) :4022-4026