2006
DOI: 10.1016/j.matbio.2006.05.004
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Testican-1 is dispensable for mouse development

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Cited by 34 publications
(26 citation statements)
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“…Interestingly, NTG significantly down-regulated testican-1, a multidomain proteoglycan that was first isolated from human seminal plasma [39], and expressed differentially in the human prostate, heart, cartilage and blood with the highest concentrations in the brain [40]. Testican contains calcium ion binding and three potential inhibitory domains (N-terminal region, thyroglobulin and follistatin-like domain), which are targeted towards three different classes of proteolytic enzymes, viz., metalloproteinase, cysteine and serine proteases.…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, NTG significantly down-regulated testican-1, a multidomain proteoglycan that was first isolated from human seminal plasma [39], and expressed differentially in the human prostate, heart, cartilage and blood with the highest concentrations in the brain [40]. Testican contains calcium ion binding and three potential inhibitory domains (N-terminal region, thyroglobulin and follistatin-like domain), which are targeted towards three different classes of proteolytic enzymes, viz., metalloproteinase, cysteine and serine proteases.…”
Section: Discussionmentioning
confidence: 99%
“…Abrogation of expression of testican-1 in mice did not reveal any demonstrable phenotypic differences during development or in adult mice (Roll et al, 2006). Histological examination of the brains of testican-1 null mice (the site of highest testican-1 expression) exhibited no significant differences from that of wild-type mice.…”
Section: Testican/spockmentioning
confidence: 91%
“…Histological examination of the brains of testican-1 null mice (the site of highest testican-1 expression) exhibited no significant differences from that of wild-type mice. Although increases in levels of testican-2 and -3 were not detected in the absence of testican-1, compensation was likely conferred for the lack of testican-1 by these related family members (Roll et al, 2006). Of note, abrogation of many matricellular proteins, have resulted in relatively mild phenotypes that are more pronounced in response to injury or challenge.…”
Section: Testican/spockmentioning
confidence: 97%
“…Considering the known functional redundancy of SPARC family of proteins in the brain and the entailing difficulties in using traditional knock-out approach to delineate functional significance of SPARC family members (Gilmour et al, 1998; McKinnon et al, 2000; Roll et al, 2006), this approach provides a useful model to analyze SC1 function in a cell type specific manner in the brain.…”
Section: Discussionmentioning
confidence: 99%