Searching for novel biomarkers using a mouse model of CLN3-Batten disease.
Searching for novel biomarkers using a mouse model of CLN3-Batten disease.
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DOI:
10.1371/journal.pone.0201470
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发表时间:
2018
期刊:
影响因子:
3.7
通讯作者:
Weimer JM
中科院分区:
文献类型:
--
作者:
Timm D;Cain JT;Geraets RD;White KA;Koh SY;Kielian T;Pearce DA;Hastings ML;Weimer JM
CLN3-Batten disease is a rare, autosomal recessive disorder involving seizures, visual, motor and cognitive decline, and premature death. The Cln3Δex7/8 mouse model recapitulates several phenotypic characteristics of the most common 1.02kb disease-associated deletion. Identification of reproducible biomarker(s) to facilitate longitudinal monitoring of disease progression and provide readouts for therapeutic response has remained elusive. One factor that has complicated the identification of suitable biomarkers in this mouse model has been that variations in animal husbandry appear to significantly influence readouts. In the current study, we cross-compared a number of biological parameters in blood from Cln3Δex7/8 mice and control, non-disease mice on the same genetic background from multiple animal facilities in an attempt to better define a surrogate marker of CLN3-Batten disease. Interestingly, we found that significant differences between Batten and non-disease mice found at one site were generally not maintained across different facilities. Our results suggest that colony variation in the Cln3Δex7/8 mouse model of CLN3-Batten disease can influence potential biomarkers of the disease.
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DOI:
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发表时间:
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期刊:
Biochimica et biophysica acta
影响因子:
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