ライフサイエンスコーパス: alpha-fodrin

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1 reby restricting access of either Sharpin or alpha-fodrin.

2 h monoclonal Abs recognizing the full-length alpha-fodrin.

3 and is proximal to the loci for gelsolin and alpha-fodrin.

4 aquaporin 5 (AQP5) and 120-kDa fragments of alpha-fodrin.

5 nalysis shows that IPF alpha is derived from alpha fodrin, a protein implicated in several diverse ce

6 In astrocytes exposed to acidic medium, alpha-fodrin, a selective endogenous substrate of calpai

7 he Aire-deficient mouse suggested a role for alpha-fodrin, a ubiquitous Ag, in the disease process.

8 une system, frequently eliciting anti-150-kd alpha-fodrin Abs in addition to the previously reported

9 s a result, adult muscle fibers contain only alpha-fodrin (alphaII) and the muscle isoform of beta-sp

10 We report here that alpha-fodrin, an abundant membrane-associated cytoskelet

11 in 2 (Ank 2), and the cytoskeletal proteins, alpha-fodrin and beta-spectrin, also selectively co-immu

12 e-8 (6-8 h) and their respective substrates, alpha-fodrin and Bid.

13 strated that t-SNAREs, NSF, actin, vimentin, alpha-fodrin and the calcium channels alpha1c and beta3

14 rates poly(ADP-ribose) polymerase (PARP) and alpha-fodrin, and DNA degradation.

15 Little is known about the anti-alpha-fodrin autoantibody response on a molecular level.

16 neoepitopes on the 150-kd cleaved product of alpha-fodrin become exposed to the immune system, freque

17 nown form of spectrin complex, consisting of alpha-fodrin, beta-fodrin, and the muscle isoform of bet

18 Antibodies to Ank 2, alpha-fodrin, beta-spectrin and IP(3)R-1 all co-immunopr

19 This antibody was shown to cross-react with alpha-fodrin breakdown products.

20 extracellular ATP induced DNA fragmentation, alpha-fodrin breakdown, and elevated levels of caspase-3

21 the epitope recognized became exposed after alpha-fodrin cleavage.

22 ent and production of 150 kD calpain-cleaved alpha-fodrin fragment, expression of IEGs, reactive astr

23 ganization of actin and the translocation of alpha-fodrin from the cytoplasm to the plasma membrane.

24 The anti-150-kd alpha-fodrin hmAbs may serve as valuable reagents for th

25 marrow of two SS donors and a panel of anti-alpha-fodrin IgGs was isolated by selection on alpha-fod

26 pha-fodrin IgGs was isolated by selection on alpha-fodrin immunoblots.

27 is elicited to a 120-kd fragment of cleaved alpha-fodrin in the majority of SS patients, but general

28 the proteolytic degradation of both GFAP and alpha-fodrin in these samples.

29 t and not with the 120-kd fragment or intact alpha-fodrin, indicating that the epitope recognized bec

30 The cytoskeletal protein alpha-fodrin is cleaved during this apoptotic process, a

31 tal actin-binding protein, alphaII-spectrin (alpha-fodrin) is cleaved into 150-, 115-, and 110-kDa fr

32 h ubiquitously expressed autoantigens (e.g., alpha-fodrin, La, and nuclear mitotic apparatus protein)

33 Included among these 11 proteins were alpha-fodrin (nonerythroid spectrin) and actin.

34 inhibited ATP-induced DNA fragmentation and alpha-fodrin proteolysis, but had no effect on ATP-induc

35 ed that 25% of SS sera exhibited this 150-kd alpha-fodrin specificity.

36 Importantly, alpha-fodrin translocation was prevented by LXA(4) but a

37 This study demonstrated that alpha-fodrin was uniquely cleaved during cytotoxic lymph

38 els of AQP5 and cleaved 120-kDa fragments of alpha-fodrin were found in tears and lacrimal gland lysa

39 pump alpha3, and IP(3)R-1 in neurons and of alpha-fodrin with NCX1 and SERCA2 in astrocytes.

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