The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Macrophages in haemopoietic and other tissues of the developing mouse detected by the monoclonal antibody F4/80
Abstract
Macrophages are widely distributed in lymphohaemo-poietic and other tissues of the normal and diseased adult, where they play an important role in host defence and repair. Although the development of haemopoiesis has been well studied in several species, the ontogeny of the mononuclear phagocyte system remains poorly understood. We have used a highly specific mAh, F4/80, to examine the distribution of mature macrophages in the developing mouse, with special reference to their presence in the haemopoietic microenvironment. Monocytes and macrophages were first seen in embryos on day 10 in the yolk sac and liver as well as in mesenchyme. In liver, spleen and bone marrow, there was expansion of this population associated with the initiation of haemopoietic on days 11,15 and 17, respectively. Macrophages in these sites formed part of the haemopoietic stroma and their extensively spread plasma membrane processes could be seen making intimate contacts with clusters of differentiating haemopoietic cells. F4/80+ cells were widely dispersed in undifferentiated mesenchymal tissue in organs such as lung, kidney and gut. Numbers of F4/80-labefled cells increased concomitantly with organ growth and local mitoses were evident, as well as actively phagocytic macrophages. Our studies establish that macrophages are among the earliest haemopoietic cells to be produced during development and that they are relatively abundant in fetal tissues in the absence of overt inflammatory stimuli. Their distribution is correlated with the sequential migration of haemopoiesis and they constitute a prominent component of the stroma in fetal liver, spleen red pulp and bone marrow. Apart from a role in haemopoietic cellular interactions, their highly developed endocytic and biosynthetic activities suggest that macrophages contribute major undefined functions during growth, turnover and modelling of fetal tissues. Abbreviations: Ab, antibody; ag, antigen; mAb, monoclonal antibody; MΦ, macrophage.
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Perry, V. H., Hume, D. A., & Gordon, S. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90215-5 · Cited by 902
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Cited by
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Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair
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Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities
McKercher, S. R., Torbett, B. E., Anderson, K. L., Henkel, G. W., Vestal, D. J., Baribault, H., Klemsz, M., Feeney, A. J., Wu, G. E., Paige, C. J., et al. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00949.x · Cited by 1,130
Microglial Activation and Chronic Neurodegeneration
Lull, M. E., & Block, M. L. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.05.014 · Cited by 1,047
“from the cells of the myeloid lineage that originate in bone marrow,(2) which occurs early in embryonic development.(3) These myeloid cells can be found within the CNS by embryonic day 8 in rodents,(4) and by week 12 of gestation in humans.”
BackgroundOrigin and differentiation of microglia
Ginhoux, F., Lim, S., Hoeffel, G., Low, D., & Huber, T. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00045 · Cited by 905
“Other studies later detected dispersed F4/80 expressing macrophages distributed within loose connective tissue surrounding the neuroectoderm in E12 rat embryos (Morris et al., 1991).”
Result
Metadata
- Authors
- Morris, L., Graham, C. F., & Gordon, S.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1991-06-01
- Volume
- 112
- Issue
- 2
- Pages
- 517-526
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W1927383279
- Cited by
- 199
- References
- 1
- FWCI
- 4.07
- Type
- journal article
- Language
- en
- Open access
- closed
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- Morris, L., Graham, C. F., & Gordon, S. (1991). Macrophages in haemopoietic and other tissues of the developing mouse detected by the monoclonal antibody F4/80. Development. https://doi.org/10.1242/dev.112.2.517
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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