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Annual Report 2006

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Fig. 6<br />

Birth weight of 11 adult SNT clones<br />

Red characters indicate individuals with bi-allelic expression of imprinting gene(s).<br />

Blue characters indicate those with mono-allelic ones.<br />

Green circle and yellow square indicate average birth weight of female and male artificially inseminated(AI).<br />

Japanese black SNT clones. Surprisingly,<br />

almost half of healthy and well-grown adult<br />

bovine SNT clones had imprinting disorder, i.e.<br />

bi-allelic expressions. Some of them were also<br />

confirmed fertile. These results were clearly<br />

indicated that imprinting disorder was common<br />

for bovine SNT clones with no apparent<br />

abnormality in adulthood. But our further<br />

analysis revealed the relationship between<br />

overweight at birth and bi-allelic disorder (Fig.<br />

6). Our results indicate that the management of<br />

imprinting will crucial for effective SNT clone<br />

reproduction.<br />

Protein-permeable scaffold of a<br />

collagen vitrigel membrane<br />

useful for reconstructing<br />

crosstalk models between two<br />

different cells<br />

We recently succeeded in converting a soft<br />

andturbiddiskofcollagengelintoastrongand<br />

transparent gel-membrane by utilizing a concept<br />

for the vitrification of heat-denatured proteins<br />

and named the novel gel in a stable condition<br />

for vitrigel. The collagen vitrigel membrane<br />

involving a nylon frame can be easily handled<br />

with tweezers, consequently it functions as a<br />

scaffold excellent for three-dimensionally<br />

culturing cells on double surfaces of it. Here, we<br />

investigated the molecular permeability of the<br />

collagen vitrigel membrane in time-course<br />

using glucose and serum proteins. The glucose<br />

added to one compartment penetrated into<br />

another compartment via the collagen vitrigel<br />

membrane and the glucose concentration of<br />

each compartment came nearly up to a plateau<br />

level within 24 hours. Serum proteins with not<br />

only low molecular weight but also high one<br />

more than 100 kDa passed gradually through<br />

the collagen vitrigel membrane (Fig. 7). These<br />

Fig. 7<br />

Permeability tests in time-course for the collagen vitrigel membrane using glucose and serum proteins<br />

Change of glucose concentration (A), quantitative clearance of FBS (B), and qualitative clearance of FBS (C) were<br />

estimated using the samples at the indicated times.

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