Abstract
The role of colony-stimulating factor-1 receptor (CSF-1R) in macrophage and organismal development has been extensively studied in mouse. Within the last decade, mutations in the CSF1R have been shown to cause rare diseases of both pediatric (Brain Abnormalities, Neurodegeneration, and Dysosteosclerosis, OMIM #618476) and adult (CSF1R-related leukoencephalopathy, OMIM #221820) onset. Here we review the genetics, penetrance, and histopathological features of these diseases and discuss to what extent the animal models of Csf1r deficiency currently available provide systems in which to study the underlying mechanisms involved.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 5049-5073 |
| Number of pages | 25 |
| Journal | FEBS Journal |
| Volume | 289 |
| Issue number | 17 |
| DOIs | |
| State | Published - Sep 2022 |
Keywords
- ALSP
- BANDDOS
- CRL
- CSF-1R
- HDLS
- POLD
- dysosteosclerosis
- leukodystrophy
- microglia
- neurodegeneration
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology
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