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Farnesol-like endogenous sesquiterpenoids in vertebrates: the probable but overlooked functional "inbrome" anti-aging counterpart of juvenile hormone of insects?.

Frontiers in endocrinology

De Loof A, Marchal E, Rivera-Perez C, Noriega FG, Schoofs L.
PMID: 25610425
Front Endocrinol (Lausanne). 2015 Jan 06;5:222. doi: 10.3389/fendo.2014.00222. eCollection 2014.

Literature on the question whether the juvenile stage of vertebrates is hormonally regulated is scarce. It seems to be intuitively assumed that this stage of development is automated, and does not require any specific hormone(s). Such reasoning mimics the...

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De Loof A, Marchal E, Rivera-Perez C, et al. Farnesol-like endogenous sesquiterpenoids in vertebrates: the probable but overlooked functional "inbrome" anti-aging counterpart of juvenile hormone of insects?. Front Endocrinol (Lausanne). 2015;5:222doi: 10.3389/fendo.2014.00222.
De Loof, A., Marchal, E., Rivera-Perez, C., Noriega, F. G., & Schoofs, L. (2014). Farnesol-like endogenous sesquiterpenoids in vertebrates: the probable but overlooked functional "inbrome" anti-aging counterpart of juvenile hormone of insects?. Frontiers in endocrinology, 5222. https://doi.org/10.3389/fendo.2014.00222
De Loof, Arnold, et al. "Farnesol-like endogenous sesquiterpenoids in vertebrates: the probable but overlooked functional "inbrome" anti-aging counterpart of juvenile hormone of insects?." Frontiers in endocrinology vol. 5 (2014): 222. doi: https://doi.org/10.3389/fendo.2014.00222
De Loof A, Marchal E, Rivera-Perez C, Noriega FG, Schoofs L. Farnesol-like endogenous sesquiterpenoids in vertebrates: the probable but overlooked functional "inbrome" anti-aging counterpart of juvenile hormone of insects?. Front Endocrinol (Lausanne). 2015 Jan 06;5:222. doi: 10.3389/fendo.2014.00222. eCollection 2014. PMID: 25610425; PMCID: PMC4285131.
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Quetiapine Inhibits Microglial Activation by Neutralizing Abnormal STIM1-Mediated Intercellular Calcium Homeostasis and Promotes Myelin Repair in a Cuprizone-Induced Mouse Model of Demyelination.

Frontiers in cellular neuroscience

Wang H, Liu S, Tian Y, Wu X, He Y, Li C, Namaka M, Kong J, Li H, Xiao L.
PMID: 26732345
Front Cell Neurosci. 2015 Dec 21;9:492. doi: 10.3389/fncel.2015.00492. eCollection 2015.

Microglial activation has been considered as a crucial process in the pathogenesis of neuroinflammation and psychiatric disorders. Several antipsychotic drugs (APDs) have been shown to display inhibitory effects on microglial activation in vitro, possibly through the suppression of elevated...

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Wang H, Liu S, Tian Y, et al. Quetiapine Inhibits Microglial Activation by Neutralizing Abnormal STIM1-Mediated Intercellular Calcium Homeostasis and Promotes Myelin Repair in a Cuprizone-Induced Mouse Model of Demyelination. Front Cell Neurosci. 2015;9:492doi: 10.3389/fncel.2015.00492.
Wang, H., Liu, S., Tian, Y., Wu, X., He, Y., Li, C., Namaka, M., Kong, J., Li, H., & Xiao, L. (2015). Quetiapine Inhibits Microglial Activation by Neutralizing Abnormal STIM1-Mediated Intercellular Calcium Homeostasis and Promotes Myelin Repair in a Cuprizone-Induced Mouse Model of Demyelination. Frontiers in cellular neuroscience, 9492. https://doi.org/10.3389/fncel.2015.00492
Wang, Hanzhi, et al. "Quetiapine Inhibits Microglial Activation by Neutralizing Abnormal STIM1-Mediated Intercellular Calcium Homeostasis and Promotes Myelin Repair in a Cuprizone-Induced Mouse Model of Demyelination." Frontiers in cellular neuroscience vol. 9 (2015): 492. doi: https://doi.org/10.3389/fncel.2015.00492
Wang H, Liu S, Tian Y, Wu X, He Y, Li C, Namaka M, Kong J, Li H, Xiao L. Quetiapine Inhibits Microglial Activation by Neutralizing Abnormal STIM1-Mediated Intercellular Calcium Homeostasis and Promotes Myelin Repair in a Cuprizone-Induced Mouse Model of Demyelination. Front Cell Neurosci. 2015 Dec 21;9:492. doi: 10.3389/fncel.2015.00492. eCollection 2015. PMID: 26732345; PMCID: PMC4685920.
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Validation of a commercially available anti-REDD1 antibody using RNA interference and REDD1-/- mouse embryonic fibroblasts.

F1000Research

Grainger DL, Kutzler L, Rannels SL, Kimball SR.
PMID: 27335637
F1000Res. 2016 Mar 01;5:250. doi: 10.12688/f1000research.7691.1. eCollection 2016.

REDD1 is a transcriptional target gene of p53 and HIF-1, and an inhibitor of mTOR (mechanistic target of rapamycin) complex 1 (mTORC1)-signaling through PP2A-dependent interaction, making it an important convergence point of both tumor suppression and cell growth pathways....

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Grainger DL, Kutzler L, Rannels SL, et al. Validation of a commercially available anti-REDD1 antibody using RNA interference and REDD1-/- mouse embryonic fibroblasts. F1000Res. 2016;5:250doi: 10.12688/f1000research.7691.1.
Grainger, D. L., Kutzler, L., Rannels, S. L., & Kimball, S. R. (2016). Validation of a commercially available anti-REDD1 antibody using RNA interference and REDD1-/- mouse embryonic fibroblasts. F1000Research, 5250. https://doi.org/10.12688/f1000research.7691.1
Grainger, Deborah L, et al. "Validation of a commercially available anti-REDD1 antibody using RNA interference and REDD1-/- mouse embryonic fibroblasts." F1000Research vol. 5 (2016): 250. doi: https://doi.org/10.12688/f1000research.7691.1
Grainger DL, Kutzler L, Rannels SL, Kimball SR. Validation of a commercially available anti-REDD1 antibody using RNA interference and REDD1-/- mouse embryonic fibroblasts. F1000Res. 2016 Mar 01;5:250. doi: 10.12688/f1000research.7691.1. eCollection 2016. PMID: 27335637; PMCID: PMC4893971.
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Regulation of IRE1α by the small molecule inhibitor 4μ8c in hepatoma cells.

Endoplasmic reticulum stress in diseases

Stewart C, Estrada A, Kim P, Wang D, Wei Y, Gentile C, Pagliassotti M.
PMID: 29098149
Endoplasmic Reticulum Stress Dis. 2017 Apr;4(1):1-10. doi: 10.1515/ersc-2017-0001. Epub 2017 Apr 27.

The unfolded protein response (UPR) is activated in response to impairments of the folding environment in the endoplasmic reticulum (ER). The most conserved arm of the UPR, inositol-requiring ER-to-nucleus signaling protein (IRE1α), has been linked to the regulation of...

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Stewart C, Estrada A, Kim P, et al. Regulation of IRE1α by the small molecule inhibitor 4μ8c in hepatoma cells. Endoplasmic Reticulum Stress Dis. 2017;4(1):1-10doi: 10.1515/ersc-2017-0001.
Stewart, C., Estrada, A., Kim, P., Wang, D., Wei, Y., Gentile, C., & Pagliassotti, M. (2017). Regulation of IRE1α by the small molecule inhibitor 4μ8c in hepatoma cells. Endoplasmic reticulum stress in diseases, 4(1), 1-10. https://doi.org/10.1515/ersc-2017-0001
Stewart, Claire, et al. "Regulation of IRE1α by the small molecule inhibitor 4μ8c in hepatoma cells." Endoplasmic reticulum stress in diseases vol. 4,1 (2017): 1-10. doi: https://doi.org/10.1515/ersc-2017-0001
Stewart C, Estrada A, Kim P, Wang D, Wei Y, Gentile C, Pagliassotti M. Regulation of IRE1α by the small molecule inhibitor 4μ8c in hepatoma cells. Endoplasmic Reticulum Stress Dis. 2017 Apr;4(1):1-10. doi: 10.1515/ersc-2017-0001. Epub 2017 Apr 27. PMID: 29098149; PMCID: PMC5661992.
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Pericellular Ca(2+) recycling potentiates thrombin-evoked Ca(2+) signals in human platelets.

Physiological reports

Sage SO, Pugh N, Farndale RW, Harper AG.
PMID: 24303163
Physiol Rep. 2013 Oct;1(5):e00085. doi: 10.1002/phy2.85. Epub 2013 Oct 11.

We have previously demonstrated that Na(+)/Ca(2+) exchangers (NCXs) potentiate Ca(2+) signaling evoked by thapsigargin in human platelets, via their ability to modulate the secretion of autocoids from dense granules. This link was confirmed in platelets stimulated with the physiological...

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Sage SO, Pugh N, Farndale RW, et al. Pericellular Ca(2+) recycling potentiates thrombin-evoked Ca(2+) signals in human platelets. Physiol Rep. 2013;1(5):e00085doi: 10.1002/phy2.85.
Sage, S. O., Pugh, N., Farndale, R. W., & Harper, A. G. (2013). Pericellular Ca(2+) recycling potentiates thrombin-evoked Ca(2+) signals in human platelets. Physiological reports, 1(5), e00085. https://doi.org/10.1002/phy2.85
Sage, Stewart O, et al. "Pericellular Ca(2+) recycling potentiates thrombin-evoked Ca(2+) signals in human platelets." Physiological reports vol. 1,5 (2013): e00085. doi: https://doi.org/10.1002/phy2.85
Sage SO, Pugh N, Farndale RW, Harper AG. Pericellular Ca(2+) recycling potentiates thrombin-evoked Ca(2+) signals in human platelets. Physiol Rep. 2013 Oct;1(5):e00085. doi: 10.1002/phy2.85. Epub 2013 Oct 11. PMID: 24303163; PMCID: PMC3841026.
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Class A scavenger receptor activation inhibits endoplasmic reticulum stress-induced autophagy in macrophage.

Journal of biomedical research

Huang H, Li X, Zhuang Y, Li N, Zhu X, Hu J, Ben J, Yang Q, Bai H, Chen Q.
PMID: 25013404
J Biomed Res. 2014 May;28(3):213-21. doi: 10.7555/JBR.28.20130105. Epub 2013 Dec 12.

Macrophage death in advanced atherosclerosis promotes plaque necrosis and destabilization. Involvement of autophagy in bulk degradation of cellular components has been recognized recently as an important mechanism for cell survival under endoplasmic reticulum (ER) stress. We previously found that...

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Huang H, Li X, Zhuang Y, et al. Class A scavenger receptor activation inhibits endoplasmic reticulum stress-induced autophagy in macrophage. J Biomed Res. 2013;28(3):213-21doi: 10.7555/JBR.28.20130105.
Huang, H., Li, X., Zhuang, Y., Li, N., Zhu, X., Hu, J., Ben, J., Yang, Q., Bai, H., & Chen, Q. (2014). Class A scavenger receptor activation inhibits endoplasmic reticulum stress-induced autophagy in macrophage. Journal of biomedical research, 28(3), 213-21. https://doi.org/10.7555/JBR.28.20130105
Huang, Hanpeng, et al. "Class A scavenger receptor activation inhibits endoplasmic reticulum stress-induced autophagy in macrophage." Journal of biomedical research vol. 28,3 (2014): 213-21. doi: https://doi.org/10.7555/JBR.28.20130105
Huang H, Li X, Zhuang Y, Li N, Zhu X, Hu J, Ben J, Yang Q, Bai H, Chen Q. Class A scavenger receptor activation inhibits endoplasmic reticulum stress-induced autophagy in macrophage. J Biomed Res. 2014 May;28(3):213-21. doi: 10.7555/JBR.28.20130105. Epub 2013 Dec 12. PMID: 25013404; PMCID: PMC4085558.
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Calpain mobilizes Atg9/Bif-1 vesicles from Golgi stacks upon autophagy induction by thapsigargin.

Biology open

Marcassa E, Raimondi M, Anwar T, Eskelinen EL, Myers MP, Triolo G, Schneider C, Demarchi F.
PMID: 28302665
Biol Open. 2017 May 15;6(5):551-562. doi: 10.1242/bio.022806.

CAPNS1 is essential for stability and function of the ubiquitous calcium-dependent proteases micro- and milli-calpain. Upon inhibition of the endoplasmic reticulum Ca

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Marcassa E, Raimondi M, Anwar T, et al. Calpain mobilizes Atg9/Bif-1 vesicles from Golgi stacks upon autophagy induction by thapsigargin. Biol Open. 2017;6(5):551-562doi: 10.1242/bio.022806.
Marcassa, E., Raimondi, M., Anwar, T., Eskelinen, E. L., Myers, M. P., Triolo, G., Schneider, C., & Demarchi, F. (2017). Calpain mobilizes Atg9/Bif-1 vesicles from Golgi stacks upon autophagy induction by thapsigargin. Biology open, 6(5), 551-562. https://doi.org/10.1242/bio.022806
Marcassa, Elena, et al. "Calpain mobilizes Atg9/Bif-1 vesicles from Golgi stacks upon autophagy induction by thapsigargin." Biology open vol. 6,5 (2017): 551-562. doi: https://doi.org/10.1242/bio.022806
Marcassa E, Raimondi M, Anwar T, Eskelinen EL, Myers MP, Triolo G, Schneider C, Demarchi F. Calpain mobilizes Atg9/Bif-1 vesicles from Golgi stacks upon autophagy induction by thapsigargin. Biol Open. 2017 May 15;6(5):551-562. doi: 10.1242/bio.022806. PMID: 28302665; PMCID: PMC5450315.
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Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion.

Nutrition research and practice

Cho JA, Park E.
PMID: 25861416
Nutr Res Pract. 2015 Apr;9(2):117-22. doi: 10.4162/nrp.2015.9.2.117. Epub 2015 Mar 06.

BACKGROUND/OBJECTIVES: Curcumin, a major component of the Curcuma species, contains antioxidant and anti-inflammatory properties. Although it was found to induce apoptosis in cancer cells, the functional role of curcumin as well as its molecular mechanism in anti-inflammatory response, particularly...

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Cho JA, Park E. Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion. Nutr Res Pract. 2015;9(2):117-22doi: 10.4162/nrp.2015.9.2.117.
Cho, J. A., & Park, E. (2015). Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion. Nutrition research and practice, 9(2), 117-22. https://doi.org/10.4162/nrp.2015.9.2.117
Cho, Jin Ah, and Park, Eunmi. "Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion." Nutrition research and practice vol. 9,2 (2015): 117-22. doi: https://doi.org/10.4162/nrp.2015.9.2.117
Cho JA, Park E. Curcumin utilizes the anti-inflammatory response pathway to protect the intestine against bacterial invasion. Nutr Res Pract. 2015 Apr;9(2):117-22. doi: 10.4162/nrp.2015.9.2.117. Epub 2015 Mar 06. PMID: 25861416; PMCID: PMC4388941.
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Hg(2+) and Cu(2+) interfere with agonist-mediated Ca(2+) signaling in isolated Mytilus digestive gland cells.

Aquatic toxicology (Amsterdam, Netherlands)

Canesi L, Ciacci C, Gallo G.
PMID: 10814802
Aquat Toxicol. 2000 May 01;49(1):1-11. doi: 10.1016/s0166-445x(99)00077-6.

The effects of mercury and copper on agonist-mediated Ca-signaling were investigated in isolated cells from the marine mussel, Mytilus galloprovincialis Lam., by single cell fluorescence microscopy. In isolated digestive gland cells, short-term exposure (10 min) to both Hg(2+), a...

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Canesi L, Ciacci C, Gallo G. Hg(2+) and Cu(2+) interfere with agonist-mediated Ca(2+) signaling in isolated Mytilus digestive gland cells. Aquat Toxicol. 2000;49(1):1-11doi: 10.1016/s0166-445x(99)00077-6.
Canesi, L., Ciacci, C., & Gallo, G. (2000). Hg(2+) and Cu(2+) interfere with agonist-mediated Ca(2+) signaling in isolated Mytilus digestive gland cells. Aquatic toxicology (Amsterdam, Netherlands), 49(1), 1-11. https://doi.org/10.1016/s0166-445x(99)00077-6
Canesi, et al. "Hg(2+) and Cu(2+) interfere with agonist-mediated Ca(2+) signaling in isolated Mytilus digestive gland cells." Aquatic toxicology (Amsterdam, Netherlands) vol. 49,1 (2000): 1-11. doi: https://doi.org/10.1016/s0166-445x(99)00077-6
Canesi L, Ciacci C, Gallo G. Hg(2+) and Cu(2+) interfere with agonist-mediated Ca(2+) signaling in isolated Mytilus digestive gland cells. Aquat Toxicol. 2000 May 01;49(1):1-11. doi: 10.1016/s0166-445x(99)00077-6. PMID: 10814802.
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A Plasma Membrane-Type Ca2+-ATPase of 120 Kilodaltons on the Endoplasmic Reticulum from Carrot (Daucus carota) Cells (Properties of the Phosphorylated Intermediate).

Plant physiology

Chen FH, Ratterman DM, Sze H.
PMID: 12231855
Plant Physiol. 1993 Jun;102(2):651-661. doi: 10.1104/pp.102.2.651.

Cytosolic Ca2+ levels are regulated in part by Ca2+-pumping ATPases that export Ca2+ from the cytoplasm; however, the types and properties of Ca2+ pumps in plants are not well understood. We have characterized the kinetic properties of a 120-kD...

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Chen FH, Ratterman DM, Sze H. A Plasma Membrane-Type Ca2+-ATPase of 120 Kilodaltons on the Endoplasmic Reticulum from Carrot (Daucus carota) Cells (Properties of the Phosphorylated Intermediate). Plant Physiol. 1993;102(2):651-661doi: 10.1104/pp.102.2.651.
Chen, F. H., Ratterman, D. M., & Sze, H. (1993). A Plasma Membrane-Type Ca2+-ATPase of 120 Kilodaltons on the Endoplasmic Reticulum from Carrot (Daucus carota) Cells (Properties of the Phosphorylated Intermediate). Plant physiology, 102(2), 651-661. https://doi.org/10.1104/pp.102.2.651
Chen, F. H., et al. "A Plasma Membrane-Type Ca2+-ATPase of 120 Kilodaltons on the Endoplasmic Reticulum from Carrot (Daucus carota) Cells (Properties of the Phosphorylated Intermediate)." Plant physiology vol. 102,2 (1993): 651-661. doi: https://doi.org/10.1104/pp.102.2.651
Chen FH, Ratterman DM, Sze H. A Plasma Membrane-Type Ca2+-ATPase of 120 Kilodaltons on the Endoplasmic Reticulum from Carrot (Daucus carota) Cells (Properties of the Phosphorylated Intermediate). Plant Physiol. 1993 Jun;102(2):651-661. doi: 10.1104/pp.102.2.651. PMID: 12231855; PMCID: PMC158825.
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Control of ion and fluid transport by putative second messengers in different segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus.

Journal of insect physiology

Xu W, Marshall AT.
PMID: 12770255
J Insect Physiol. 2000 Jan;46(1):21-31. doi: 10.1016/s0022-1910(99)00097-9.

The differences in second messenger control of secretion were investigated in the distal and main segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus. Secretion by the main segment was considerably increased by corpora cardiaca extract...

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Xu W, Marshall AT. Control of ion and fluid transport by putative second messengers in different segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus. J Insect Physiol. 2000;46(1):21-31doi: 10.1016/s0022-1910(99)00097-9.
Xu, W., & Marshall, A. T. (2000). Control of ion and fluid transport by putative second messengers in different segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus. Journal of insect physiology, 46(1), 21-31. https://doi.org/10.1016/s0022-1910(99)00097-9
Xu, W, and Marshall, A T.. "Control of ion and fluid transport by putative second messengers in different segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus." Journal of insect physiology vol. 46,1 (2000): 21-31. doi: https://doi.org/10.1016/s0022-1910(99)00097-9
Xu W, Marshall AT. Control of ion and fluid transport by putative second messengers in different segments of the Malpighian tubules of the black field cricket Teleogryllus oceanicus. J Insect Physiol. 2000 Jan;46(1):21-31. doi: 10.1016/s0022-1910(99)00097-9. PMID: 12770255.
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Signalling steps in apoptosis by ether lipids.

Apoptosis : an international journal on programmed cell death

Smets LA, Van Rooij H, Salomons GS.
PMID: 14634326
Apoptosis. 1999 Dec;4(6):419-27. doi: 10.1023/a:1009644208512.

We have investigated the mechanisms of induction of apoptosis by the antineoplastic ether lipid ET-18-OCH3 (ALP) in sensitive S49wt mouse lymphoma cells and ALP-resistant S49ar variants, both with wild-type p53, and in related L1210 cells with mutated p53. Ether...

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Smets LA, Van Rooij H, Salomons GS. Signalling steps in apoptosis by ether lipids. Apoptosis. 1999;4(6):419-27doi: 10.1023/a:1009644208512.
Smets, L. A., Van Rooij, H., & Salomons, G. S. (1999). Signalling steps in apoptosis by ether lipids. Apoptosis : an international journal on programmed cell death, 4(6), 419-27. https://doi.org/10.1023/a:1009644208512
Smets, L A, et al. "Signalling steps in apoptosis by ether lipids." Apoptosis : an international journal on programmed cell death vol. 4,6 (1999): 419-27. doi: https://doi.org/10.1023/a:1009644208512
Smets LA, Van Rooij H, Salomons GS. Signalling steps in apoptosis by ether lipids. Apoptosis. 1999 Dec;4(6):419-27. doi: 10.1023/a:1009644208512. PMID: 14634326.
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Showing 1 to 12 of 282 entries