Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment

Spanel-Borowski K, Nowicki M, Borlak J, Trapphoff T, Eichenlaub-Ritter U (2013)
Cells Tissues Organs 197(1): 77-88.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Spanel-Borowski, Katharina; Nowicki, Marcin; Borlak, Juergen; Trapphoff, Tom; Eichenlaub-Ritter, UrsulaUniBi
Abstract / Bemerkung
Objective: Multilamellar bodies associated with an organized endoplasmic reticulum (ER) arise in various somatic cell types, and a subtype called multivesicular bodies is described in oocytes. Both entities, so far undetermined in significance, may occur in oocytes of follicles under oxidative stress. In preovulatory follicles, oxidative stress appears to be caused by oxidized low-density lipoprotein (ox-LDL). Method: Cultures of preantral mouse follicles were treated with 100 mu g/ml ox-LDL or normal LDL (n-LDL) for 12-48 h or for 12 days during antral follicle growth followed by in vitro ovulation and harvest of cumulus oophorus complexes (COCs) with metaphase II (MII) oocytes on day 13. Preantral follicles, COCs, or MII oocytes were immunostained with anti-tubulin antibody or stained with actin-binding phalloidin for confocal microscopy. Ultrathin sections were prepared for electron microscopy. Results: Preantral follicles exposed to nLDL or ox-LDL developed normally, and MII oocytes in COCs possessed normal spindles with well-aligned chromosomes. In contrast, treated cumulus cells underwent apoptosis. Only the ox-LDL-treated preantral follicle oocytes showed ER-derived multilamellar bodies (EMBs) of type I, consisting of rough ER membranes for the envelope. The MII oocytes of COCs showed type II EMBs consisting of smooth/vesicular ER and were more prominent after ox-LDL than after n-LDL exposure. Degenerating mitochondria were prominent in oocytes of the ox-LDL group and judged as a sign of oxidative stress. Conclusion: Oxidative stress presumably induces damage of proteins and organelles in the oocytes. The EMBs might sequester the damaged structures for oocyte survival. Thus, EMBs could represent a novel form of autophagy. Copyright (C) 2012 S. Karger AG, Basel
Stichworte
Oxidative stress; Oxidized low-density lipoprotein; cultures; Follicle; Oocyte; Multilamellar bodies; Organized endoplasmic reticulum; Autophagy
Erscheinungsjahr
2013
Zeitschriftentitel
Cells Tissues Organs
Band
197
Ausgabe
1
Seite(n)
77-88
ISSN
1422-6421
eISSN
1422-6421
Page URI
https://pub.uni-bielefeld.de/record/2553262

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Spanel-Borowski K, Nowicki M, Borlak J, Trapphoff T, Eichenlaub-Ritter U. Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment. Cells Tissues Organs. 2013;197(1):77-88.
Spanel-Borowski, K., Nowicki, M., Borlak, J., Trapphoff, T., & Eichenlaub-Ritter, U. (2013). Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment. Cells Tissues Organs, 197(1), 77-88. doi:10.1159/000340039
Spanel-Borowski, Katharina, Nowicki, Marcin, Borlak, Juergen, Trapphoff, Tom, and Eichenlaub-Ritter, Ursula. 2013. “Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment”. Cells Tissues Organs 197 (1): 77-88.
Spanel-Borowski, K., Nowicki, M., Borlak, J., Trapphoff, T., and Eichenlaub-Ritter, U. (2013). Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment. Cells Tissues Organs 197, 77-88.
Spanel-Borowski, K., et al., 2013. Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment. Cells Tissues Organs, 197(1), p 77-88.
K. Spanel-Borowski, et al., “Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment”, Cells Tissues Organs, vol. 197, 2013, pp. 77-88.
Spanel-Borowski, K., Nowicki, M., Borlak, J., Trapphoff, T., Eichenlaub-Ritter, U.: Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment. Cells Tissues Organs. 197, 77-88 (2013).
Spanel-Borowski, Katharina, Nowicki, Marcin, Borlak, Juergen, Trapphoff, Tom, and Eichenlaub-Ritter, Ursula. “Endoplasmic Reticulum-Derived Multilamellar Bodies in Oocytes of Mouse Follicle Cultures under Oxidized Low-Density Lipoprotein Treatment”. Cells Tissues Organs 197.1 (2013): 77-88.

47 References

Daten bereitgestellt von Europe PubMed Central.

MHC class II compartments in human dendritic cells undergo profound structural changes upon activation.
Barois N, de Saint-Vis B, Lebecque S, Geuze HJ, Kleijmeer MJ., Traffic 3(12), 2002
PMID: 12453152
Elevated levels of oxidized low-density lipoprotein and of catalase activity in follicular fluid of obese women.
Bausenwein J, Serke H, Eberle K, Hirrlinger J, Jogschies P, Hmeidan FA, Blumenauer V, Spanel-Borowski K., Mol. Hum. Reprod. 16(2), 2009
PMID: 19729414
Oxidized low density lipoprotein (ox-LDL) binding to ox-LDL receptor-1 in endothelial cells induces the activation of NF-kappaB through an increased production of intracellular reactive oxygen species.
Cominacini L, Pasini AF, Garbin U, Davoli A, Tosetti ML, Campagnola M, Rigoni A, Pastorino AM, Lo Cascio V, Sawamura T., J. Biol. Chem. 275(17), 2000
PMID: 10777555
Reactive oxygen species level in follicular fluid--embryo quality marker in IVF?
Das S, Chattopadhyay R, Ghosh S, Ghosh S, Goswami SK, Chakravarty BN, Chaudhury K., Hum. Reprod. 21(9), 2006
PMID: 16861701
Roles of reactive oxygen species and antioxidants in ovarian toxicity.
Devine PJ, Perreault SD, Luderer U., Biol. Reprod. 86(2), 2012
PMID: 22034525
Lectin-like oxidized low-density lipoprotein receptor-1-mediated autophagy in human granulosa cells as an alternative of programmed cell death.
Duerrschmidt N, Zabirnyk O, Nowicki M, Ricken A, Hmeidan FA, Blumenauer V, Borlak J, Spanel-Borowski K., Endocrinology 147(8), 2006
PMID: 16690797
Chloral hydrate induced spindle aberrations, metaphase I arrest and aneuploidy in mouse oocytes.
Eichenlaub-Ritter U, Betzendahl I., Mutagenesis 10(6), 1995
PMID: 8596466
Mitochondria and the autophagy-inflammation-cell death axis in organismal aging.
Green DR, Galluzzi L, Kroemer G., Science 333(6046), 2011
PMID: 21868666
Biogenesis of multilamellar bodies via autophagy.
Hariri M, Millane G, Guimond MP, Guay G, Dennis JW, Nabi IR., Mol. Biol. Cell 11(1), 2000
PMID: 10637306
Effects of low O2 and ageing on spindles and chromosomes in mouse oocytes from pre-antral follicle culture.
Hu Y, Betzendahl I, Cortvrindt R, Smitz J, Eichenlaub-Ritter U., Hum. Reprod. 16(4), 2001
PMID: 11278227
Receptor downregulation and multivesicular-body sorting.
Katzmann DJ, Odorizzi G, Emr SD., Nat. Rev. Mol. Cell Biol. 3(12), 2002
PMID: 12461556
Annulate lamellae: a last frontier in cellular organelles.
Kessel RG., Int. Rev. Cytol. 133(), 1992
PMID: 1374369
Autophagy: from phenomenology to molecular understanding in less than a decade.
Klionsky DJ., Nat. Rev. Mol. Cell Biol. 8(11), 2007
PMID: 17712358
Peptide-based interactions with calnexin target misassembled membrane proteins into endoplasmic reticulum-derived multilamellar bodies.
Korkhov VM, Milan-Lobo L, Zuber B, Farhan H, Schmid JA, Freissmuth M, Sitte HH., J. Mol. Biol. 378(2), 2008
PMID: 18367207
The lipid composition of autophagic vacuoles regulates expression of multilamellar bodies.
Lajoie P, Guay G, Dennis JW, Nabi IR., J. Cell. Sci. 118(Pt 9), 2005
PMID: 15840653
Contribution of culture media to oxidative stress and its effect on human oocytes.
Martin-Romero FJ, Miguel-Lasobras EM, Dominguez-Arroyo JA, Gonzalez-Carrera E, Alvarez IS., Reprod. Biomed. Online 17(5), 2008
PMID: 18983749
3-D Structure of multilaminar lysosomes in antigen presenting cells reveals trapping of MHC II on the internal membranes.
Murk JL, Lebbink MN, Humbel BM, Geerts WJ, Griffith JM, Langenberg DM, Verreck FA, Verkleij AJ, Koster AJ, Geuze HJ, Kleijmeer MJ., Traffic 5(12), 2004
PMID: 15522096
Autophagy is activated for cell survival after endoplasmic reticulum stress.
Ogata M, Hino S, Saito A, Morikawa K, Kondo S, Kanemoto S, Murakami T, Taniguchi M, Tanii I, Yoshinaga K, Shiosaka S, Hammarback JA, Urano F, Imaizumi K., Mol. Cell. Biol. 26(24), 2006
PMID: 17030611
From oogonia to mature oocytes: inactivation of the maternal centrosome in humans.
Sathananthan AH, Selvaraj K, Girijashankar ML, Ganesh V, Selvaraj P, Trounson AO., Microsc. Res. Tech. 69(6), 2006
PMID: 16718650
Autophagy in innate and adaptive immunity against intracellular pathogens.
Schmid D, Dengjel J, Schoor O, Stevanovic S, Munz C., J. Mol. Med. 84(3), 2006
PMID: 16501849
Granulosa cell subtypes vary in response to oxidized low-density lipoprotein as regards specific lipoprotein receptors and antioxidant enzyme activity.
Serke H, Bausenwein J, Hirrlinger J, Nowicki M, Vilser C, Jogschies P, Hmeidan FA, Blumenauer V, Spanel-Borowski K., J. Clin. Endocrinol. Metab. 95(7), 2010
PMID: 20444928
Granulosa cell subtypes respond by autophagy or cell death to oxLDL-dependent activation of the oxidized lipoprotein receptor 1 and toll-like 4 receptor.
Serke H, Vilser C, Nowicki M, Hmeidan FA, Blumenauer V, Hummitzsch K, Losche A, Spanel-Borowski K., Autophagy 5(7), 2009
PMID: 19730000
Reactive oxygen species are indispensable in ovulation.
Shkolnik K, Tadmor A, Ben-Dor S, Nevo N, Galiani D, Dekel N., Proc. Natl. Acad. Sci. U.S.A. 108(4), 2011
PMID: 21220312
Formation of stacked ER cisternae by low affinity protein interactions.
Snapp EL, Hegde RS, Francolini M, Lombardo F, Colombo S, Pedrazzini E, Borgese N, Lippincott-Schwartz J., J. Cell Biol. 163(2), 2003
PMID: 14581454
Morphological investigations on follicular atresia in canine ovaries.
Spanel-Borowski K., Cell Tissue Res. 214(1), 1981
PMID: 7193522
Ovulation as danger signaling event of innate immunity.
Spanel-Borowski K., Mol. Cell. Endocrinol. 333(1), 2010
PMID: 21163330
Preantral follicle culture as a novel in vitro assay in reproductive toxicology testing in mammalian oocytes.
Sun F, Betzendahl I, Shen Y, Cortvrindt R, Smitz J, Eichenlaub-Ritter U., Mutagenesis 19(1), 2004
PMID: 14681309
Assembly of nuclear pore complexes and annulate lamellae promotes normal pronuclear development in fertilized mammalian oocytes.
Sutovsky P, Simerly C, Hewitson L, Schatten G., J. Cell. Sci. 111 ( Pt 19)(), 1998
PMID: 9730977
Cellular and molecular aspects of ovarian follicle ageing.
Tatone C, Amicarelli F, Carbone MC, Monteleone P, Caserta D, Marci R, Artini PG, Piomboni P, Focarelli R., Hum. Reprod. Update 14(2), 2008
PMID: 18239135
Female reproductive dysfunction during ageing: role of methylglyoxal in the formation of advanced glycation endproducts in ovaries of reproductively-aged mice.
Tatone C, Carbone MC, Campanella G, Festuccia C, Artini PG, Talesa V, Focarelli R, Amicarelli F., J. Biol. Regul. Homeost. Agents 24(1), 2010
PMID: 20385072
Evidence that carbonyl stress by methylglyoxal exposure induces DNA damage and spindle aberrations, affects mitochondrial integrity in mammalian oocytes and contributes to oocyte ageing.
Tatone C, Heizenrieder T, Di Emidio G, Treffon P, Amicarelli F, Seidel T, Eichenlaub-Ritter U., Hum. Reprod. 26(7), 2011
PMID: 21558076
The role of autophagy during the oocyte-to-embryo transition.
Tsukamoto S, Kuma A, Mizushima N., Autophagy 4(8), 2008
PMID: 18849666
Autophagy is essential for preimplantation development of mouse embryos.
Tsukamoto S, Kuma A, Murakami M, Kishi C, Yamamoto A, Mizushima N., Science 321(5885), 2008
PMID: 18599786
Mitochondria removal by autophagy.
Wang K, Klionsky DJ., Autophagy 7(3), 2011
PMID: 21252623
Proteome of mouse oocytes at different developmental stages.
Wang S, Kou Z, Jing Z, Zhang Y, Guo X, Dong M, Wilmut I, Gao S., Proc. Natl. Acad. Sci. U.S.A. 107(41), 2010
PMID: 20876089
Mechanisms of oxidative stress in porcine oocytes and the role of anti-oxidants.
Whitaker BD, Knight JW., Reprod. Fertil. Dev. 20(6), 2008
PMID: 18671917
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