Target intelligence / Profile preview

Solute carrier organic anion transporter family member 1C1 (SLCO1C1)

Target
SLCO1C1
Molecular classification
Transporter, Solute carrier protein, Transmembrane protein, Major facilitator superfamily
01

Overview

SLCO1C1, also known as Organic anion transporter 1C1 (OATP1C1), is a transmembrane protein belonging to the solute carrier family of organic anion transporters. It specifically facilitates sodium-independent, high-affinity transport of thyroid hormones such as L-thyroxine (T4), reverse triiodothyronine (rT3), and L-thyroxine sulfate (T4S) into brain tissues, especially astrocytes and glial cells. The transporter plays a crucial role in regulating the availability of thyroid hormones, which are essential for neuronal development and function. SLCO1C1 operates across the blood–brain barrier and is especially important for hormone signaling in the central nervous system. It exhibits 12 transmembrane domains and functions independently of sodium ions, with a transport mechanism similar to other major facilitator family proteins (“rocker-switch”). Genetic mutations in SLCO1C1 can cause severe CNS effects due to impaired hormone uptake and conversion, and altered expression can contribute to neurological and endocrine disease manifestations. Recently, SLCO1C1 is being investigated for its potential to facilitate targeted drug delivery to the brain, including as a vehicle for anti-inflammatory prodrugs in glial cells.

Other names
OATP1C1OATP-14OATP-FSLC21A14OATPFOAT-RP-5OATP-RP5Organic anion transporter 1C1Organic anion transporter FOrganic anion-transporting polypeptide 14Organic anion transporter polypeptide-related protein 5Thyroxine transporter
02

Mechanism of action

Sodium-independent high-affinity transport of specific organic anions (especially thyroid hormones) across cellular membranes; uptake into astrocytes and glia, enabling hormone conversion and CNS signaling

03

Biological functions

Thyroid hormone transportOrganic anion uptakeRegulation of intracellular thyroid hormone availabilityRegulation of hormone signalingBlood-brain barrier transportSkeletal muscle regenerationCellular uptake into astrocytes and glia
04

Disease associations

Neurological disorders (e.g., psychomotor retardation due to impaired thyroid hormone transport)Congenital hypothyroidismFatigue and depression in hyperthyroidismAutism spectrum disorderDeafness (autosomal recessive 62)
05

Safety considerations

Potential off-target substrate transportdrug–drug interactions for molecules with high affinity for SLCO1C1genetic polymorphisms leading to altered hormone delivery to CNSpossible effects in brain development and function
06

Interacting drugs

L-thyroxine (T4)

6 more in the full profile.

07

Biomarkers

Mutations or polymorphisms of SLCO1C1 gene (e.g., Asp252Asn associated with impaired function)altered SLCO1C1 expression (e.g., depression, fatigue in hyperthyroidism)

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