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bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this version posted March 4, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0...
It is made available under a CC-BY-NC-ND 4.0 International license . Introduction Lung cancer and specifically lung adenocarcinoma (LUAD) remains the leading cause of cancer death world-wide. New therapies that molecularly target driver mutations have improved patient outcome. However, the development of resistance mut...
In KRASG12D-driven tumors, NKX2-1 deletion increases phospho-ERK and accelerates progression to invasive carcinoma and metastasis (8, 24, 27). Clinically, low NKX2-1 expression portends a poor prognosis (28-30). We reasoned that in addition to beginning the de-differentiation process, a repressed-NKX2-1 status might dr...
We found that NKX2-1 loss in LUAD clinical samples and cell lines correlates with reduced DUSP6. Further, NKX2-1 directly induces DUSP6 expression and limits tumor cell proliferation, migration, invasion, and tumor growth metastasis. While DUSP6 knockout can be toxic, it abrogates the effects of NKX2-1 on cell prolifer...
1D). NKX2-1 did not induce SPRY2 protein in any cell line (A549 p=0.617, H1299 p=0.098, H23 p=0.493, Fig. 1D). We also tested if NKX2-1 induces DUSP6 or SPRY2 in a murine LUAD cell line derived from KRASG12D; TP53Null; NKX2-1Null mouse tumors (3658 cells, (24)). Indeed, qRT-PCR again showed that exogenous NKX2-1 increa...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license . lines, including A549 and 3658 cells (50). However, A549 and 3658 cells are ...
In our LUAD cells with re- introduction of NKX2-1, we found that the p-ERK induced by stimulation with RAS pathway agonists EGF or PMA trended lower in cells expressing NKX2-1 compared to cells with empty vector (Fig. S2C, S2D, not significant). The small change is consistent with the previous studies on DUSP6. NKX2-1 ...
5 out of 9 mice with A549-V tumors exhibited micrometastases versus 0 out of 9 mice with A549-NKX2-1 tumors (Fig. 3B). IHC showed that tumors lacking NKX2-1 exhibit low DUSP6 expression and high p-ERK (Fig. 3C). In contrast, tumors with NKX2-1 reconstitution exhibited high DUSP6 expression and reduced p-ERK (Fig. 3C). ...
S4B). In H1299 cells, DUSP6 loss did not change cell proliferation (Day 6 p=0.38), but SPRY2 loss increased proliferation (Day 5 p=7.5x10-6, Fig. S4D). This suggests that in cell culture, A549 and H1299 cells engage compensatory signaling to limit the effects of DUSP6 loss. However, under these unpressured growth condi...
To test this, we generated subcutaneous tumors with the A549 DUSP6 knockouts harboring inducible TRE-NKX2-1 and GFP-luciferase. After the tumors reached 150-400 mm3 (5 weeks for control bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this version posted March 4, 2021. The copyright holder for this pr...
It is made available under a CC-BY-NC-ND 4.0 International license . expression reduced tumor size and p-ERK in this system (Fig. 5F). In summary, DUSP6 and SPRY2 are sufficient to limit tumorigenesis in the genetically engineered model of LUAD. Discussion Activating mutations in EGFR, KRAS and BRAF initiate LUAD tumor...
Further, DUSP6 but not SPRY2, protein was significantly upregulated upon introduction of NKX2-1 into human LUAD cell lines, both in vitro and in xenografts. However, in the genetically engineered mouse tumors, Nkx2-1 deletion caused a loss of SPRY2 along with a loss of DUSP6. This suggests that NKX2-1 works through DUS...
Similarly, LUAD cells with acquired resistance to EGFR inhibitors are addicted to the inhibitor-dampened ERK activity such that inhibitor withdrawal induces toxic ERK hyperactivation (65). Lineage heterogeneity promotes chemoresistance (26). Models of tumors with heterogeneous ERK activity show that ERK heterogeneity c...
A. Proliferation of A549 and H1299 cells. Significance from one-way ANOVA. B. and C. Random-walk migration velocity and directionality of H1299 cells upon NKX2-1 expression and MEK inhibition (Selumetinib 10 µM). Velocity is Mean Squared Displacement. Significance from bioRxiv preprint doi: https://doi.org/10.1101/202...
Figure S3. NKX2-1 is required for DUSP6 expression and ERK activity in vivo. A. and B. Representative IHC images of KRASG12D;NKX2-1WT and KRASG12D;NKX2-1Null tumors: NKX2-1 target pro-SPB, DUSP6, SPRY2, p-ERK and effector p-RSK and p-S6 levels. Scale bars: 100 µm. n=6 mice tamoxifen, n=6 mice corn oil injections. Figur...
Relative expression compared to total ERK. Means and SD from n=3 independent experiments. C. IHC for DUSP6 in TRE- Spry2 tumors and SPRY2 in TRE-DUSP6 tumors. Methods Histology and IHC Human tissue microarrays were formalin fixed and paraffin embedded: US Biomax BCS04017, BCS04017a, LC10014a. Arrays were stained for NK...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license . with AscI and EcoRI, and ligated into a modified pBabe-Puro retroviral backb...
2011 PMID 21458673 MGI 4950589 Dr. Scott Lowe (MSK, New York, New York) Cell line 293T ATCC # CRL-11268 Cell line Cell line Phoenix-Ampho A549 ATCC ATCC # CRL-3213 # CCL-185 Cell line H1299 ATCC # CRL-5803 Cell line Cell line Virus Plasmid Plasmid H23 3658 Ad5CMV-FlpO MSCV-NKX2-1 pGL3-191p pGL3-508p ATCC Snyder et al. ...
Cells were tested for mycoplasma every 3-4 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this version posted March 4, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. ...
Cells were selected with blasticidin for 1 week. NKX2-1 expression was induced in cells with 1 µg/ml of doxycycline and confirmed by Western blotting. Ultracentrifugation at 25,000 rpm for 2 hrs was necessary to concentrate pCDH-TRE-DUSP6 and pCDH-TRE-SPRY2 virus for in vivo infection. Fluorescence-activated cell sorti...
Cells were transfected the next day with pRenilla (Addgene) and empty pGL3 vector or pGL3 vector containg the DUSP6 promoter regions 191p and 508p using Lipofectamine 2000 (Invitrogen). After 24 hours the Dual-Glo Luciferase Assay System (Promega) was used and luminescence was measured by the Synergy HT microplate read...
Spheroids bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this version posted March 4, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-B...
Genetically engineered mice and tumor initiation Under University of Utah IACUC #18-08005, mice harboring KRasfrtSfrt-G12D/+;Nkx2-1f/f; RosafrtSfrt-CreERT2 alleles were infected intratracheally with 1 x 107 pfu/mouse Ad5CMV-FlpO (University of Iowa Viral Vector Core). FlpO recombined Frt-STOP-Frt for simultaneous KRASG...
Nature. 2014;511(7511):543-50. doi: 10.1038/nature13385. PubMed PMID: 25079552. 3. Ding L, Getz G, Wheeler DA, Mardis ER, McLellan MD, Cibulskis K, Sougnez C, Greulich H, Muzny DM, Morgan MB, Fulton L, Fulton RS, Zhang Q, Wendl MC, Lawrence MS, Larson DE, Chen K, Dooling DJ, Sabo A, Hawes AC, Shen H, Jhangiani SN, Lewi...
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and clinical outcome in non-small-cell lung cancer. N Engl J Med. 2007;356(1):11-20. Epub 2007/01/05. doi: 10.1056/NEJMoa060096. PubMed PMID: 17202451. 40. Okudela K, Yazawa T, Woo T, Sakaeda M, Ishii J, Mitsui H, Shimoyamada H, Sato H, Tajiri M, Ogawa N, Masuda M, Takahashi T, Sugimura H, Kitamura H. Down-regulation o...
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It is made available under a CC-BY-NC-ND 4.0 International license . 2019;25(13):4117-27. Epub 2019/04/03. doi: 10.1158/1078-0432.CCR-18-3224. PubMed PMID: 30936125; PMCID: PMC6606396. 63. Shojaee S, Caeser R, Buchner M, Park E, Swaminathan S, Hurtz C, Geng H, Chan LN, Klemm L, Hofmann WK, Qiu YH, Zhang N, Coombes KR, ...
Image-guided genomics of phenotypically heterogeneous populations reveals vascular signalling during symbiotic collective cancer invasion. Nat Commun. 2017;8:15078. Epub 2017/05/13. doi: 10.1038/ncomms15078. PubMed PMID: 28497793; PMCID: PMC5437311. bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this...
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.04.433941 ; this version posted March 4, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0...
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Caspase-2 regulates S-phase cell cycle events to protect f...
Thus, our data supports a model where caspase-2 regulates cell cycle events to protect from the accumulation of DNA damage independently of its pro-apoptotic function. 4 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 2021. The copyright holder for this preprint (which w...
This has been noted for caspase-2 dependent apoptosis that can be either p53-dependent12-14 or p53-independent.15, 16 Caspase-2 has been shown to be activated by several different inducers of DNA damage including etoposide, cisplatin, and camptothecin.13, 17-19 However, apoptosis can often proceed in the absence of cas...
Mouse embryonic fibroblasts (MEF) were grown in the same medium supplemented with sodium pyruvate (1 mM), 1X non-essential amino acids, and beta-mercaptoethanol (55 µM). Litter-matched Casp2+/+ and Casp2-/- MEF were generated and transduced with E1A and Ras as previously described.19 Briefly, early passage MEF were sim...
Cells were imaged using one of two microscope systems. The first is a spinning disk confocal microscope (Carl Zeiss MicroImaging, Thornwood, NY, USA), equipped with a CSU-X1A 5000 spinning disk unit (Yokogawa Electric Corporation, Japan), multi laser module with wavelengths of 458 nm, 488 nm, 514 nm, and 561 nm, and an...
Images were smoothed by Gaussian method followed by separation using Otsu with an adaptive thresholding strategy. Cells were then declumped by shape and automatically counted. For quantitation of γ H2AX foci, the number of foci per cell was calculated from RGB TIFF images using FoCo, a graphical user interface that use...
Cells were washed in BD Perm/Wash buffer and centrifuged at 300 x g between each step. To uncover the BrdU epitope, the cells were treated with DNAse (30 µg per 106 cells) for 1 h at 37°C, washed in BD Perm/Wash buffer, and centrifuged at 300 x g. The cells were then incubated in a 1:50 dilution of FITC-labeled anti-Br...
ImageJ software was used to analyze the DNA fibers. For each data set, about 300 fibers were counted for stalled forks, new origins, or elongated forks. Viability assay Casp2+/+ and Casp2-/- MEF were plated in a 24-well plate at the indicated densities. After four days colonies were visualized by staining overnight wit...
To confirm these results, we used BrdU/7AAD staining to determine the cell cycle profiles of cycling Casp2+/+ and Casp2-/- MEF and found that Casp2-/- cells had significantly more cells in S-phase and less cells in G1-phase compared to the Casp2+/+ cells (Figure 1D, E). The increased proportion of S-phase cells suggest...
This indicates that caspase-2 activation does not coincide G2/M phase of the cell cycle, but is activated in G1 and early S-phase. Loss of caspase-2 results in S-phase specific chromosomal aberrations and delayed exit 16 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 20...
HU induces replication fork stalling and S-phase arrest by depleting the available nucleotide pool for DNA polymerases.34 Cells were pulse-labeled with 5-iododeoxyuridine (IdU), treated with HU for 2 h to induce replicative stress, and then washed and pulse-labeled with 5-chlorodeoxyuridine (CldU). Individual DNA fiber...
We measured checkpoint activation in Casp2+/+ and Casp2–/– MEF treated with HU (Figure 5A). Chk1 was phosphorylated immediately after HU release to a similar extent with and without caspase-2 and minimal differences in Chk1 phosphorylation between the two cell lines were noted over time. Interestingly, phosphorylation ...
ATM phosphorylation was not induced by HU in the U2OS cells. In HeLa cells and in U2OS cells, we detected strong Chk2 phosphorylation in response to HU and 20 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 2021. The copyright holder for this preprint (which was not cert...
22 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Discussion Here we report that caspase-2 is activated ...
This would suggest that caspase-2 functions downstream of, or independently of, ATR and Chk1 in response to stalled replication forks. Chk1 has been proposed as an inhibitor of caspase-2 in response to IR-induced DNA damage.15 Inhibition of Chk1 potentiates caspase-2 dependent apoptosis by derepressing ATM-mediated pho...
Treatment with inducers of G2/M arrest including nocodazaole and Plk1 inhibition has been shown to induce caspase-2-dependent apoptosis as a mechanism to remove aneuploidy cells.54 However, it is not clear whether caspase-2 regulates cell cycle during the DNA damage response through activation of the same pathway compo...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. independently of caspase-2 to activate ATR, but the nucleolar PIDDosome is required for efficient resolution of stalled forks and prevention of DSBs. To fully u...
*p<0.05. (C) Representative images are shown from the 0 h and 72 h time points. Nuclei are shown in blue. Bar, 200 µm. (D) Untreated, cycling litter- matched Casp2+/+ and Casp2-/- E1A/Ras MEF were stained with BrdU/7-AAD and analyzed by flow cytometry. Representative flow plots are shown. (E) The percentage of cells in...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. three times. **p<0.01. (B) Representative images of metaphase spread of untreated (-) or irradiated Casp2+/+ and Casp2-/- MEF. Red arrows show breaks; blue arro...
Bar, 50 µm. 36 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437768 ; this version posted March 30, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. ed Figure 5. Loss of caspase-2 does not im...
Results are an average of 3 independent experiments plus or minus standard deviation. (D) Casp2+/+ and Casp2-/- MEF stably expressing vector or Bcl-XL were treated with the indicated doses of camptothecin for 4 h or 24 h. Apoptosis was measured at 24 h by Annexin V staining. Results are the average of 3 independent exp...
J Biol Chem 277: 29803-29809. 14 Baptiste-Okoh N, Barsotti A, Prives C (2008). A role for caspase 2 and PIDD in the process of p53-mediated apoptosis. . Proc Natl Acad Sci U S A 105: 1937-1942. 15 Sidi S, Sanda T, Kennedy RD, Hagen AT, Jette CA, Hoffmans R et al (2008). Chk1 suppresses a caspase-2 apoptotic response to...
Mol Cell Biol 23: 8363-8376. 29 Hunt CR, Dix DJ, Sharma GG, Pandita RK, Gupta A, Funk M et al (2004). Genomic instability and enhanced radiosensitivity in Hsp70.1- and Hsp70.3-deficient mice. Mol Cell Biol 24: 899-911. 30 Baliga BC, Read SH, Kumar S (2004). The biochemical mechanism of caspase-2 activation. Cell Death ...
Journal of Biological Chemistry 280: 4649- 4655. 45 Guo Y, Srinivasula SM, Druilhe A, Fernandes-Alnemri T, Alnemri ES (2002). Caspase-2 induces apoptosis by releasing proapoptotic proteins from mitochondria. J Biol Chem 277: 13430-13437. 46 Bonzon C, Bouchier-Hayes L, Pagliari LJ, Green DR, Newmeyer DD (2006). Caspase-...
ATM, ATR, and DNA-PK: The Trinity at the Heart of the DNA Damage Response. Mol Cell 66: 801-817. 60 Sidi S, Sanda T, Kennedy RD, Hagen AT, Jette CA, Hoffmans R et al (2008). Chk1 Suppresses a Caspase-2 Apoptotic Response to DNA Damage that Bypasses p53, Bcl- 2, and Caspase-3. Cell 133: 864-877. 61 Abraham RT (2001). Ce...
Nucleic Acids Research 46: 1847-1859. 75 Ando K, Parsons MJ, Shah RB, Charendoff CI, Paris SL, Liu PH et al (2017). NPM1 directs PIDDosome-dependent caspase-2 activation in the nucleolus. Journal of Cell Biology 216: 1795-1810. 76 Logette E, Schuepbach-Mallepell S, Eckert MJ, Leo XH, Jaccard B, Manzl C et al (2011). PI...
bioRxiv preprint doi: https://doi.org/10.1101/2021.06.30.450599 ; this version posted July 1, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Title: Genome-wide association study and functional validati...
Barker Foundation, The McCune Foundation Acknowledgments: The authors would like to acknowledge the neuropathology core of the Massachusetts Alzheimer Disease Research Center, the Biosample Management Repository at Genentech/Roche, the brain repository at UCI, Knight Alzheimer Disease Research Center Neuropathology Cor...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 21 Departments of Pathology (Neuropathology) and Neurological Sciences, Rush University Medical Center, Chicago IL, USA 22 Department of Psychiatry, Alzheimer's...
The pathogenesis of PART is unknown, but evidence suggests it is associated with β genes that promote tau pathology as well as others that protect from A toxicity. Here, we performed a genetic association study in an autopsy cohort of individuals with PART (n=647) using Braak neurofibrillary tangle stage as a quantitat...
Given the similarities between PART and AD NFTs, PART as a diagnostic construct would have greater value if it were shown to arise β independently 14,15. Alternatively, PART might be a component of the AD spectrum, and A pathology might have eventually developed in such individuals had they lived longer 15,16. Thus, th...
In collaboration with twenty-one domestic and international brain biorepositories, we performed the first genome-wide association study in PART and compared our findings to known tauopathy risk loci. We then localized expression of candidate genes in our strongest risk locus (chromosome 4q28.2) using single cell RNA-se...
Genomic DNA was isolated and purified using magnetic particles. DNA quality control was performed using a nanodrop spectrophotometer (concentration > 50ng/µl, 260/280 ratio 1.7-2.2). Genotyping was performed using single nucleotide polymorphism (SNP) microarrays (Infinium Global tau bioRxiv preprint doi: https://doi.o...
μ Formalin-fixed paraffin-embedded tissue sections (5 m) on charged slides were baked at 70ºC and immunohistochemistry (IHC) was performed on a Ventana Benchmark XT automatic stainer (Rouche, Tucson, AZ). Antigen retrieval was done using citric acid buffer (CC1) for 1 hr followed by primary antibody incubation for appr...
Samples were incubated on ice for 30 min, centrifuged at 1000 x g for 10 min and the supernatant was collected as an input and used for immunoprecipitation. In a microcentrifuge tube, 70 ul of supernatant, Lysis buffer (930 µl) and 2 µg of either JADE1 antisera or anti-0N tau antisera (EPR21726, Abcam, Cambridge, MA) w...
Samples were incubated on ice for 30 min, centrifuged at 1000 x g for 10 min, and supernatant was collected. Reaction mixtures (51 µul) consisted of 39 µl of supernatant, 1 µl of protease inhibitor cocktail, 5 µl of 10X NEBuffer for protein metallophosphatases, 5 µl of 10 mM MnCl2, 1 µl of lambda protein phosphatase (N...
μ TUNEL was performed on 4 m formalin-fixed paraffin-embedded fly heads. Quantification of TUNEL- positive nuclei was performed throughout the entire brain using DAB-based detection and bright field microscopy. Fly eye phenotype scoring was performed blindly using light microscopy (n=16). The blinded rater semi-quantit...
Using Braak stage as a quantitative trait revealed a genom me wide β associated signal on chromosome 4q28.2 (Fig. 1a, rs56405341; linear regression =0.35, st standard error=0.06, p=4.82 × 10-8) and suggestive signals in 14 other loci (Table 2 and Supplementary Table le 3). Our λ model, which adjusted for age, sex, and ...
All rights reserved. No reuse allowed without permission. = 9.0 × 10-6, OR = 0.043) 53. Taken together, these two independent genetic studies in AD sugg ggest the signal in our GWAS might not be spurious. We also examined candidate SNPs previously found to be associated with AD and prog ogressive supranuclear palsy (PS...
2d-f). SCLT1 and C4orf33 had nominal expression levels in a substantially smaller percentage of neurons. Taken together, these data suggest increased JADE1 expression is unique to specific populations of neurons which also contain NFTs. Because we did not observe significant differences in C4orf33 or SCLT1 expression a...
A Western blot analysis revealed a strong signal in both brain regions and diseases for JADE1S, but no bands were observed in the expected weight for JADE1L, indicating the observed signal is specific to the short isoform of JADE1 (Fig. 4b). This signal is in agreement with the immunohistochemical data given we did not...
We used a Drosophila model that overexpresses human mutant 0N4R tau55 as well as RNAi-mediated reduction of rhinoceros (rno), the highest matched JADE1 human ortholog in Drosophila. We first blindly evaluated the fly eye phenotype using a semi-quantitative assessment of eye size, roughness, overall shape, and conical s...
This accumulation of JADE1 protein in NFT is not specific to PART but occurs in AD and all tauopathies with accumulation of 4R isoforms, but not in Pick disease which is a 3R tauopathy, indicating that this is generally a shared feature. We also show that JADE1 binds 0N4R tau, an isoform proposed to be a critical drive...
Eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3) encodes an endoplasmic reticulum (ER) membrane protein critical for the unfolded protein response (UPR)83,84. Activation of the UPR has been observed and positively correlated with tau pathology, but not with A β plaque burden, in the hippocampus of ag...
Our biochemical studies suggest that JADE1 protein specifically interacts with 0N4R tau that is phosphorylated on epitopes known to be hyperphosphorylated in NFT. Our proximity ligation assay confirms the direct interaction between JADE1 protein and tau. Studies using cryo-EM and mass spectrometry have shown the ultras...
While Braak staging is highly reproducible, with one report showing that across brains and raters the kappa score was greater than 0.90 108, it is a semiquantitative (ordinal) variable. Further studies using a more quantitative approach to measuring tau burden that we have shown more closely align with functional clini...
Neurons with and without neurofibrillary tangles from huma an post- mortem brains samples were separated using fluorescence-activated cell sorting and single-cel ell RNA- sequencing was performed. (a) In 2 unique excitatory neuronal populations JADE1 mRNA was sign differentially expressed in the tangle bearing neurons ...
(o) Double staining of a PART entorhinal cortex showing the absence of JADE1 1 (brown) staining in early pre-tangles, but the presence of p-tau (pink, see inset). (p) peptide competition demon onstrating the antisera for JADE1 is specifically binding to the correct epitope give then absence of positive staining, g, but...
bioRxiv preprint doi: https://doi.org/10.1101/2021.06.30.450599 ; this version posted July 1, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. References: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 ...
Acta Neuropathologica 128, 767-772, doi:10.1007/s00401-014-1356-1 (2014). Duyckaerts, C. et al. PART is part of Alzheimer disease. Acta Neuropathologica 129, 749-756, doi:10.1007/s00401-015-1390-7 (2015). Lafirdeen, A. S. M. et al. Biomarker profiles of Alzheimer's disease and dynamic of the association between cerebro...
Mol Neurodegener 13, 41, doi:10.1186/s13024-018-0270-8 (2018). Santa-Maria, I. et al. The MAPT H1 haplotype is associated with tangle-predominant dementia. Acta neuropathologica 124, 693-704, doi:10.1007/s00401-012-1017-1 (2012). Mungas, D., Tractenberg, R., Schneider, J. A., Crane, P. K. & Bennett, D. A. A 2-process m...
The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 44 45 46 47 Price, A. L. et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38, 904-909, doi:10.1038...
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The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 89 90 Lambert, J. C. et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet 45, 1452-U1206, doi:10....
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bioRxiv preprint doi: https://doi.org/10.1101/2021.07.26.453735 ; this version posted July 26, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0...
1A). The EO conformation has ~1000-fold higher binding affinity for ligand than the two closed conformations and is the final competent state to mediate cell adhesion and migration (Li & Springer, 2018; Li et al, 2017; Schürpf & Springer, 2011). Many previous studies have emphasized the importance of force in regulatin...
For two classes of force-regulated adhesion molecules, each of which have a single low- affinity state and a single high-affinity state, selectins (Phan et al, 2006) and FimH (Yakovenko, 2015), the low-affinity conformation has a faster on-rate for ligand than the high-affinity conformation. If subsequent conformationa...
RESULTS Ligand-binding kinetics of intact α4β1 and α5β1 on cell surfaces. We measured binding kinetics of intact α4β1 on Jurkat cells to two fluorescently labeled ligands, a phenylureide derivative of Leu-Asp-Val-Pro (FITC-LDVP) and a fragment of vascular cell adhesion molecule (VCAM) containing its first two domains (...
2D). Association and dissociation both became markedly slower when only the EO conformation of α4β1 was present (Fig. 2E). To address the generality of these results, we studied another integrin and cell type by measuring binding of a fluorescently-labeled two-domain fragment of fibronectin (Alexa488- Fn39-10) to intac...
We utilized bio-layer interferometry (BLI) (Wallner et al, 2013) to measure the kinetics of binding of an ectodomain fragment of α5β1 to the biotin-labeled Fn39-10 fragment of fibronectin immobilized on streptavidin biosensors (Fig. 4). The ectodomain was truncated just prior to the transmembrane domains of the α5 and ...
5-6). Dissociation of the ligand from the EO state is very slow as shown above and is negligible in our experimental time scale. At high Fab mAb13 concentrations, when the EO ligand-bound state (EOL) converts to either BCL or ECL (they are grouped together here as (CL), mAb13 Fab binds and prevents back-conversion ...
The underlying assumption for deconvoluting the kinetics of the closed states is that if integrin conformational transition kinetics are sufficiently fast so that the populations of the three integrin states do not deviate significantly during our experiments from the equilibrium values of the populations, then measure...
We found that despite ~1,000 lower affinity, the closed states, BC and EC, of two β1 distinct integrins have markedly higher on-rates than the EO state. These findings have important implications for the sequence of events that occur when integrins interact with ligands, as discussed in the Integrin Activation section ...
In our previous work, we compared affinities measured with at least two Fabs specific for the closed, open, and extended states and for each state compared Fabs that bound to different domains. The results showed no significant differences between affinities measured with different Fabs. Here, we compared two Fabs used...