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. Author manuscript; available in PMC: 2022 Mar 8.
Published in final edited form as: Ageing Res Rev. 2021 Oct 9;72:101485. doi: 10.1016/j.arr.2021.101485

Table 1.

Genetically modified mouse models

Genetic manipulation Peripheral Phenotype CNS Phenotype (if reported) Authors
HAS1 KO Impedes formation of retrocalcaneal bursa Mild seizure phenotype Sikes et al., 2018; Arranz et al., 2014
HAS2 KO Severe cardiac and vascular abnormalities; incompatible with normal embryonic development Camenisch et al., 2000
Conditional HAS2 KO Under Prx1-Cre: shortened limbs, duplicated proximal phalanges, abnormal growth plates, lack of formation of secondary ossification centers, defective synovial cavities Under Nestin-Cre: mild seizure phenotype, reduction in cortical HA and lack of HA deposition in major fiber tracts Matsumoto et al., 2009; Arranz et al., 2014
HAS3 KO Protection from ventilator induced lung inflammation; protection from dextran sodium sulfate induced colitis Seizures, reduction in HA content in hippocampus Bai et al., 2005; Kessler et al., 2015; Arranz et al., 2014
HAS1/3 KO Abnormal and accelerated wound healing and enhanced inflammation around induced lesions Mack et al., 2012;
HYAL1 KO Mild mucopolysaccharidosis Martin et al., 2008; Bourguignon et al., 2016
HYAL2 KO Cranio-vertebral skeletal abnormalities, thrombocytopenia, hemolysis, HA content increase in plasma and liver Jadin et al., 2008; Bourguignon et al., 2016
HYAL3 KO No gross phenotypic change, normal HA levels in serum, but mild changes in alveolar structure Atmuri et al., 2008