» Articles » PMID: 9108108

Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice

Overview
Specialty Science
Date 1997 Apr 15
PMID 9108108
Citations 218
Authors
Affiliations
Soon will be listed here.
Abstract

Glial cells are thought to derive embryologically from either myeloid cells of the hematopoietic system (microglia) or neuroepithelial progenitor cells (astroglia and oligodendrocytes). However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells present in the brain since the fetal stage of development, or if there is further input into such adult brains from cells originating outside the central nervous system. To test the ability of hematopoietic cells to contribute to the central nervous system, we have transplanted adult female mice with donor bone marrow cells genetically marked either with a retroviral tag or by using male donor cells. Using in situ hybridization histochemistry, a continuing influx of hematopoietic cells into the brain was detected. Marrow-derived cells were already detected in the brains of mice 3 days after transplant, and their numbers increased over the next several weeks, exceeding 14,000 cells per brain in several animals. Marrow-derived cells were widely distributed throughout the brain, including the cortex, hippocampus, thalamus, brain stem, and cerebellum. When in situ hybridization histochemistry was combined with immunohistochemical staining using lineage-specific markers, some bone marrow-derived cells were positive for the microglial antigenic marker F4/80. Other marrow-derived cells surprisingly expressed the astroglial marker glial fibrillary acidic protein. These results indicate that some microglia and astroglia arise from a precursor that is a normal constituent of adult bone marrow.

Citing Articles

The two-sided battlefield of tumour-associated macrophages in glioblastoma: unravelling their therapeutic potential.

Xiong J, Zhou X, Su L, Jiang L, Ming Z, Pang C Discov Oncol. 2024; 15(1):590.

PMID: 39453528 PMC: 11511804. DOI: 10.1007/s12672-024-01464-5.


Glial cells in the mammalian olfactory bulb.

Zhao D, Hu M, Liu S Front Cell Neurosci. 2024; 18:1426094.

PMID: 39081666 PMC: 11286597. DOI: 10.3389/fncel.2024.1426094.


Update on the mechanism of microglia involvement in post-stroke cognitive impairment.

Zeng T, Liu J, Zhang W, Yu Y, Ye X, Huang Q Front Aging Neurosci. 2024; 16:1366710.

PMID: 38887610 PMC: 11181926. DOI: 10.3389/fnagi.2024.1366710.


Targeting the Multiple Complex Processes of Hypoxia-Ischemia to Achieve Neuroprotection.

Maiza A, Hamoudi R, Mabondzo A Int J Mol Sci. 2024; 25(10).

PMID: 38791487 PMC: 11121719. DOI: 10.3390/ijms25105449.


Molecular Mechanisms in Pathophysiology of Mucopolysaccharidosis and Prospects for Innovative Therapy.

Ago Y, Rintz E, Musini K, Ma Z, Tomatsu S Int J Mol Sci. 2024; 25(2).

PMID: 38256186 PMC: 10816168. DOI: 10.3390/ijms25021113.


References
1.
Young 3rd W, Mezey E, Siegel R . Vasopressin and oxytocin mRNAs in adrenalectomized and Brattleboro rats: analysis by quantitative in situ hybridization histochemistry. Brain Res. 1986; 387(3):231-41. DOI: 10.1016/0169-328x(86)90029-x. View

2.
Eglitis M, Kantoff P, Gilboa E, Anderson W . Gene expression in mice after high efficiency retroviral-mediated gene transfer. Science. 1985; 230(4732):1395-8. DOI: 10.1126/science.2999985. View

3.
Perry V, Gordon S . Macrophages and microglia in the nervous system. Trends Neurosci. 1988; 11(6):273-7. DOI: 10.1016/0166-2236(88)90110-5. View

4.
Giulian D, Chen J, Ingeman J, George J, Noponen M . The role of mononuclear phagocytes in wound healing after traumatic injury to adult mammalian brain. J Neurosci. 1989; 9(12):4416-29. PMC: 6569632. View

5.
Lillien L, Raff M . Differentiation signals in the CNS: type-2 astrocyte development in vitro as a model system. Neuron. 1990; 5(2):111-9. DOI: 10.1016/0896-6273(90)90301-u. View