Primitive Embryonic Macrophages are Required for Coronary Development and Maturation. Issue 10 (13th May 2016)
- Record Type:
- Journal Article
- Title:
- Primitive Embryonic Macrophages are Required for Coronary Development and Maturation. Issue 10 (13th May 2016)
- Main Title:
- Primitive Embryonic Macrophages are Required for Coronary Development and Maturation
- Authors:
- Leid, Jamison
Carrelha, Joana
Boukarabila, Hanane
Epelman, Slava
Jacobsen, Sten E.W.
Lavine, Kory J. - Abstract:
- Abstract : Rationale: : It is now recognized that macrophages residing within developing and adult tissues are derived from diverse progenitors including those of embryonic origin. Although the functions of macrophages in adult organisms are well studied, the functions of macrophages during organ development remain largely undefined. Moreover, it is unclear whether distinct macrophage lineages have differing functions. Objective: : To address these issues, we investigated the functions of macrophage subsets resident within the developing heart, an organ replete with embryonic-derived macrophages. Methods and Results: : Using a combination of flow cytometry, immunostaining, and genetic lineage tracing, we demonstrate that the developing heart contains a complex array of embryonic macrophage subsets that can be divided into chemokine (C-C motif) receptor 2 − and chemokine (C-C motif) receptor 2 + macrophages derived from primitive yolk sac, recombination activating gene 1 + lymphomyeloid, and Fms-like tyrosine kinase 3 + fetal monocyte lineages. Functionally, yolk sac–derived chemokine (C-C motif) receptor 2 − macrophages are instrumental in coronary development where they are required for remodeling of the primitive coronary plexus. Mechanistically, chemokine (C-C motif) receptor 2 − macrophages are recruited to coronary blood vessels at the onset of coronary perfusion where they mediate coronary plexus remodeling through selective expansion of perfused vasculature. WeAbstract : Rationale: : It is now recognized that macrophages residing within developing and adult tissues are derived from diverse progenitors including those of embryonic origin. Although the functions of macrophages in adult organisms are well studied, the functions of macrophages during organ development remain largely undefined. Moreover, it is unclear whether distinct macrophage lineages have differing functions. Objective: : To address these issues, we investigated the functions of macrophage subsets resident within the developing heart, an organ replete with embryonic-derived macrophages. Methods and Results: : Using a combination of flow cytometry, immunostaining, and genetic lineage tracing, we demonstrate that the developing heart contains a complex array of embryonic macrophage subsets that can be divided into chemokine (C-C motif) receptor 2 − and chemokine (C-C motif) receptor 2 + macrophages derived from primitive yolk sac, recombination activating gene 1 + lymphomyeloid, and Fms-like tyrosine kinase 3 + fetal monocyte lineages. Functionally, yolk sac–derived chemokine (C-C motif) receptor 2 − macrophages are instrumental in coronary development where they are required for remodeling of the primitive coronary plexus. Mechanistically, chemokine (C-C motif) receptor 2 − macrophages are recruited to coronary blood vessels at the onset of coronary perfusion where they mediate coronary plexus remodeling through selective expansion of perfused vasculature. We further demonstrate that insulin like growth factor signaling may mediate the proangiogenic properties of embryonic-derived macrophages. Conclusions: : Together, these findings demonstrate that the embryonic heart contains distinct lineages of embryonic macrophages with unique functions and reveal a novel mechanism that governs coronary development. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Circulation research. Volume 118:Issue 10(2016)
- Journal:
- Circulation research
- Issue:
- Volume 118:Issue 10(2016)
- Issue Display:
- Volume 118, Issue 10 (2016)
- Year:
- 2016
- Volume:
- 118
- Issue:
- 10
- Issue Sort Value:
- 2016-0118-0010-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-05-13
- Subjects:
- flow cytometry -- fms-like tyrosine kinase 3 -- macrophages -- monocytes -- yolk sac
Cardiovascular system -- Periodicals
Blood -- Circulation -- Periodicals
Blood Circulation
Cardiovascular System
Vascular Diseases
Sang -- Circulation -- Périodiques
Appareil cardiovasculaire -- Périodiques
612.1 - Journal URLs:
- http://circres.ahajournals.org/ ↗
http://www.circresaha.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCRESAHA.115.308270 ↗
- Languages:
- English
- ISSNs:
- 0009-7330
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.300000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 66.xml