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. Author manuscript; available in PMC: 2024 Jun 5.
Published in final edited form as: Biochim Biophys Acta Mol Basis Dis. 2021 Jan 24;1867(5):166085. doi: 10.1016/j.bbadis.2021.166085

Table 1.

Tissue distributions of RARs and RXRs in mammals, and phenotypes of isotype-specific knockout in mouse.

Receptor
(gene
symbol)
Expression pattern Knockout phenotype Ref
Most abundant Liver General Liver specific
RARα (NR1B1) Widely expressed Parenchyma, endothelia, kupffer and stellate cell Postnatal lethality and some abnormalities including testis degeneration [16-21]
RARβ (NR1B2) Lung, intestine, genitalia, epithelia, limbs, brain. Parenchyma, endothelial, Kupffer and stellate cell No obvious external and internal abnormalities [19,22-24]
PARγ (NR1B3) Cartilage, embryo, epidermis, skeleton Parenchyma, endothelial, Kupffer and stellate cell Postpartum lethality and growth deficiency. (male sterility; Agenesis of the ocular Harderian gland and homeotic transformations of the axial skeleton) [19,25-27]
RXRα (NR2B1) Liver, kidney, spleen, placenta, epidermis and a variety of visceral tissues Parenchyma, endothelial, kupffer and stellate cell Died in utero and displayed myocardial and ocular malformations Disturbed lipid metabolism; a deficiency of Epo expression in the fetal liver; impaired regenerative capacity [19,28-30]
RXRβ (NR2B2) Widely expressed Parenchyma, endothelial, Kupffer and stellate cell Normal. Except male infertility. [19,30-32]
RXRγ (NR2B3) Muscle, brain Parenchyma, endothelial, and Kupffer cell Postnatal lethality and some abnormalities including homeotic transformation [19,27,32,33]

Note: The expression levels of all RXR subtypes is higher than all RAR subtypes in all liver cells.