Go forth or multiply
نویسنده
چکیده
A cell can move and reproduce, but it usually can't do both simultaneously. As Makagiansar et al. report on page 155, the pattern of phosphorylation on a membrane proteoglycan helps determine whether cells grow or go. The phosphory-lation differences direct the molecule to distinct parts of the cell membrane. Even cancer cells have to slow down before they can divide, as do normal progenitor cells such as those that spawn oligodendrocytes in the brain. Evidence suggests that NG2, a proteoglycan in the cell membrane , enables cells to choose which action to perform. Cancer cells and progenitor cells manufacture NG2, for example, but most other cells don't. Three years ago, the researchers showed that affi xing a phosphate to a particular amino acid in NG2 changed cell behavior. Specifi cally, phosphor-ylating the threonine at position 2256 spurred cells to crawl. Makagiansar et al. wanted to discern what happens after phosphorylation of another threonine, found at position 2314. This addition inhibited movement. The researchers also discovered that whereas phosphorylation of threonine-2256 checked cell proliferation, phosphory-lation at the other position promoted it. The difference in function might stem from a shift in location. Instead of signal-ing directly, NG2 relays its messages through β1 integrin. The team showed that, after phosphorylation of threonine-2256, NG2 and β1 integrin clustered at the front edge of the cell. But after phosphorylation of threonine-2314, NG2 and β1 integrin gathered in small spikes on the cell's upper surface. Overall, the results indicate that phosphorylation at each site triggers a contrasting response from the cell. If both sites were modifi ed, threonine-2256 seemed to prevail , and the cell got going. The researchers now hope to work out how phos-phorylation at the two sites nudges NG2 into different locations. One possibility is that phosphorylation alters how NG2 interacts with scaffolding molecules such as MUPP1 and GRIP1 that control signaling interactions in the cytoplasm. A s it morphs from a squirming maggot into a buzzing adult, a fruit fl y jettisons its juvenile salivary glands. On page 85, Yin et al. show how the insects get rid of a protective protein, allowing the glands to break down at the right time. The research helps clarify how certain tissues prepare themselves to die. During metamorphosis, a larva's obsolete internal organs degenerate, and replacements sprout. Surging quantities of the steroid hormone ecdysone spur the salivary glands and other juvenile structures to melt …
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عنوان ژورنال:
- The Journal of Cell Biology
دوره 178 شماره
صفحات -
تاریخ انتشار 2007