Macrophage polarization in pathology

Macrophages are cells of the innate immunity constituting the mononuclear phagocyte system and endowed with remarkable different roles essential for defense mechanisms, development of tissues, and homeostasis. They derive from hematopoietic precursors and since the early steps of fetal life populate...

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Published inCellular and molecular life sciences : CMLS Vol. 72; no. 21; pp. 4111 - 4126
Main Authors Sica, Antonio, Erreni, Marco, Allavena, Paola, Porta, Chiara
Format Journal Article
LanguageEnglish
Published Basel Springer Basel 01.11.2015
Springer Nature B.V
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Online AccessGet full text
ISSN1420-682X
1420-9071
1420-9071
DOI10.1007/s00018-015-1995-y

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Abstract Macrophages are cells of the innate immunity constituting the mononuclear phagocyte system and endowed with remarkable different roles essential for defense mechanisms, development of tissues, and homeostasis. They derive from hematopoietic precursors and since the early steps of fetal life populate peripheral tissues, a process continuing throughout adult life. Although present essentially in every organ/tissue, macrophages are more abundant in the gastro-intestinal tract, liver, spleen, upper airways, and brain. They have phagocytic and bactericidal activity and produce inflammatory cytokines that are important to drive adaptive immune responses. Macrophage functions are settled in response to microenvironmental signals, which drive the acquisition of polarized programs, whose extremes are simplified in the M1 and M2 dichotomy. Functional skewing of monocyte/macrophage polarization occurs in physiological conditions (e.g., ontogenesis and pregnancy), as well as in pathology (allergic and chronic inflammation, tissue repair, infection, and cancer) and is now considered a key determinant of disease development and/or regression. Here, we will review evidence supporting a dynamic skewing of macrophage functions in disease, which may provide a basis for macrophage-centered therapeutic strategies.
AbstractList Macrophages are cells of the innate immunity constituting the mononuclear phagocyte system and endowed with remarkable different roles essential for defense mechanisms, development of tissues, and homeostasis. They derive from hematopoietic precursors and since the early steps of fetal life populate peripheral tissues, a process continuing throughout adult life. Although present essentially in every organ/tissue, macrophages are more abundant in the gastro-intestinal tract, liver, spleen, upper airways, and brain. They have phagocytic and bactericidal activity and produce inflammatory cytokines that are important to drive adaptive immune responses. Macrophage functions are settled in response to microenvironmental signals, which drive the acquisition of polarized programs, whose extremes are simplified in the M1 and M2 dichotomy. Functional skewing of monocyte/macrophage polarization occurs in physiological conditions (e.g., ontogenesis and pregnancy), as well as in pathology (allergic and chronic inflammation, tissue repair, infection, and cancer) and is now considered a key determinant of disease development and/or regression. Here, we will review evidence supporting a dynamic skewing of macrophage functions in disease, which may provide a basis for macrophage-centered therapeutic strategies.
Macrophages are cells of the innate immunity constituting the mononuclear phagocyte system and endowed with remarkable different roles essential for defense mechanisms, development of tissues, and homeostasis. They derive from hematopoietic precursors and since the early steps of fetal life populate peripheral tissues, a process continuing throughout adult life. Although present essentially in every organ/tissue, macrophages are more abundant in the gastro-intestinal tract, liver, spleen, upper airways, and brain. They have phagocytic and bactericidal activity and produce inflammatory cytokines that are important to drive adaptive immune responses. Macrophage functions are settled in response to microenvironmental signals, which drive the acquisition of polarized programs, whose extremes are simplified in the M1 and M2 dichotomy. Functional skewing of monocyte/macrophage polarization occurs in physiological conditions (e.g., ontogenesis and pregnancy), as well as in pathology (allergic and chronic inflammation, tissue repair, infection, and cancer) and is now considered a key determinant of disease development and/or regression. Here, we will review evidence supporting a dynamic skewing of macrophage functions in disease, which may provide a basis for macrophage-centered therapeutic strategies.Macrophages are cells of the innate immunity constituting the mononuclear phagocyte system and endowed with remarkable different roles essential for defense mechanisms, development of tissues, and homeostasis. They derive from hematopoietic precursors and since the early steps of fetal life populate peripheral tissues, a process continuing throughout adult life. Although present essentially in every organ/tissue, macrophages are more abundant in the gastro-intestinal tract, liver, spleen, upper airways, and brain. They have phagocytic and bactericidal activity and produce inflammatory cytokines that are important to drive adaptive immune responses. Macrophage functions are settled in response to microenvironmental signals, which drive the acquisition of polarized programs, whose extremes are simplified in the M1 and M2 dichotomy. Functional skewing of monocyte/macrophage polarization occurs in physiological conditions (e.g., ontogenesis and pregnancy), as well as in pathology (allergic and chronic inflammation, tissue repair, infection, and cancer) and is now considered a key determinant of disease development and/or regression. Here, we will review evidence supporting a dynamic skewing of macrophage functions in disease, which may provide a basis for macrophage-centered therapeutic strategies.
Author Allavena, Paola
Porta, Chiara
Sica, Antonio
Erreni, Marco
Author_xml – sequence: 1
  givenname: Antonio
  surname: Sica
  fullname: Sica, Antonio
  email: antonio.sica@humanitasresearch.it, antonio.sica@pharm.unipmn.it
  organization: Department of Pharmaceutical Sciences, Università del Piemonte Orientale “Amedeo Avogadro”, Humanitas Clinical and Research Center
– sequence: 2
  givenname: Marco
  surname: Erreni
  fullname: Erreni, Marco
  organization: Humanitas Clinical and Research Center
– sequence: 3
  givenname: Paola
  surname: Allavena
  fullname: Allavena, Paola
  organization: Humanitas Clinical and Research Center
– sequence: 4
  givenname: Chiara
  surname: Porta
  fullname: Porta, Chiara
  organization: Department of Pharmaceutical Sciences, Università del Piemonte Orientale “Amedeo Avogadro”
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26210152$$D View this record in MEDLINE/PubMed
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IngestDate Thu Aug 21 18:35:00 EDT 2025
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Wed Aug 13 11:05:41 EDT 2025
Mon Jul 21 06:02:44 EDT 2025
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Tue Jul 01 00:54:59 EDT 2025
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Issue 21
Keywords Tissue damage
Inflammation
Tissue homeostasis
Macrophage polarization
Disease
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PublicationTitle Cellular and molecular life sciences : CMLS
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SubjectTerms Biochemistry
Biomedical and Life Sciences
Biomedicine
Cell Biology
Cell Polarity
Cellular biology
Disease
Helicobacter Infections - pathology
HIV Infections - pathology
Homeostasis
Humans
Hypersensitivity - pathology
Infections - microbiology
Infections - parasitology
Infections - pathology
Infections - virology
Life Sciences
Macrophages - pathology
Macrophages - physiology
Neoplasms - pathology
Obesity - metabolism
Obesity - pathology
Pathology
Review
Sepsis - pathology
Tissues
Tuberculosis - pathology
Wound Healing
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