The food poison microbe Clostridium perfringens produces a toxin that is useful

Question

The food poison microbe Clostridium perfringens produces a toxin that is useful for studies of epithelial sheet formation. A portion of the toxin binds to the extracellular domain of certain claudin isoforms and prevents their homotypic interactions. This toxin binds to claud.n-4, which happens to be expressed in the tight junctions formed by the clonal dog kidney cell line called MDCK. The presence of tight junctions in MDCK cells can be of MDCK cell can be assayed using microscopy and by measurement of the paracellular electrical resistance between the apical and basolateral sides of MDCK ceil sheets (more resistance = tighter seal). A. Addition of the toxin to the media of MDCK cells reduces the average number of stands "stitching together" the membranes in tight junctions by about 50%. However, the remaining 50% of strands appear perfectly normal. If claudin-4 .s involved in tight junction formation in these cells, why would 50% of strands be completely resistant to the toxin? B. Careful addition of toxin only to the basolateral surface of an MDCK cell sheet causes a partial drop in paracellular resistance (indicating a weaker, but still functional seal), while addition of toxin to only the apical surface causes no decrease in resistance. What does this tell you about the organization of different isoforms of tight junction molecules m a tight junction?

Explanation / Answer

A)

Clostridium perfringens enterotoxin (CPE) induced disruption of tight junction is dose dependent (Reference 1). So, we can assume that at the given concentration CPE could disrupt only 50% of strands. Increase in CPE concentration would perhaps disrupt the remaining strands

B)

Addition of CPE to basolateral side disrupted tight junctions whereas addition at apical side did not. Tight junctions are located between apical and basolateral sides of the cell and are closer to apical side than basal side.

We can assume that there claudins in the basal side of the cells in the form of non-polymerized molecules (opposed to polymerized strands in tight junctions) and they can act as receptors.

References:

1)

Sonoda, N., Furuse, M., Sasaki, H., Yonemura, S., Katahira, J., Horiguchi, Y. and Tsukita, S., 1999. Clostridium perfringens enterotoxin fragment removes specific claudins from tight junction strands. The Journal of cell biology, 147(1), pp.195-204.

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