Membrane damage and repair 7470_Week_8_Weisled… · Membrane repair is a conserved physiologic...
Transcript of Membrane damage and repair 7470_Week_8_Weisled… · Membrane repair is a conserved physiologic...
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Membrane damage and repairNoah Weisleder, Ph.D.
Department of Physiology and Cell Biology
Davis Heart and Lung Research Institute
The Ohio State University
[email protected](614) 292‐5321
M N il d B k C ll d Ti R h 2001
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Topics for the class:What is cell membrane repair?
Why do cells need to actively repair their membranes?
How do cells repair the plasma membrane at the molecular level?
What are the pathologic consequences of defective membrane repair?
Can membrane repair be targeted as a therapeutic approach?
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Ca2+‐triggered patch model for membrane repair
Membrane disruption
Ca2+ entry through the injury site
Ca2+‐triggering vesicle exocytosis
Vesicle fusion
Patch formation; membrane resealing
Nature Reviews Molecular Cell Biology 6, 499-505 (June 2005)
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Intracellular vesicles participate in membrane patching following damage
McNeil and Baker, Cell and Tissue Research, 2001
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Evidence of membrane resealing in living mammalian cells
Li, et al. Hum. Mol. Genet. (15 May 2006)15 (10): 1610‐1622. Lovering, et al. AJP Cell April 2011 C803‐C813
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Methods to measure membrane repair• Dye exclusion/entry into the cell
– UV laser damage– Physical disruption of the membrane– Histological analysis of tissues (Evans blue, IgG entry)
• Leak of a biomarker out of the cell– Creatine kinase– Troponins– Lactate dehydrogenase
• Changes in membrane biophysical conditions
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Membrane repair is a conserved physiologic process in multiple tissues
Organ Type of mechanical force Principal cells stressed
Cell wounding (proportion of cells involved)
Reference
Skeletal muscle Aperiodic, highly variable intensity: shear, stretch
Skeletal muscle cells (myocytes) Yes (3-20%) McNeil and Khakee,
1992
Cardiac muscle Cyclic: shear, stretch Cardiac myocytes Yes (25%) Clarke et al., 1995
SkinAperiodic, highly variable intensity: shear, stretch, compression
Epidermal cells, Fibroblasts, etc. Yes (3-6%) McNeil and Ito, 1990
Gastrointestinal tract Cyclic: shear, stretch Epithelial cells, smooth
muscle cells
Yes, epithelial cells (% not measured)
McNeil and Ito, 1989
Vascular (conducting) Constant and cyclic:shear Endothelial cells,
smooth muscle cells
Yes, aortic endothelial cells
(6.5%)Yu and McNeil, 1992
Respiratory Cyclic: stretchEpithelial cells, endotherlial cells, smooth muscle cells
Alveolar cells (2-30% in
mechanically ventilated lung)
Gajic et al., 2003
Peripheral nervous Aperiodic, highly variable intensity: shear Inner ear cells Yes, hair cells (%
not measured) Mulroy et al., 1998
McNeil and Steinhardt, Annu Rev Cell Dev Biol. 2003
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Topics for the class:What is cell membrane repair?
Why do cells need to actively repair their membranes?
How do cells repair the plasma membrane at the molecular level?
What are the pathologic consequences of defective membrane repair?
Can membrane repair be targeted as a therapeutic approach?
![Page 9: Membrane damage and repair 7470_Week_8_Weisled… · Membrane repair is a conserved physiologic process in multiple tissues Organ Type of mechanical force Principal cells stressed](https://reader033.fdocuments.in/reader033/viewer/2022041603/5e324dd387dca6413522f346/html5/thumbnails/9.jpg)
Necessity of membrane repair in eukaryotic cellsCellular insult
Cell Membrane
Membrane Patch = Cell Survival
MG53 drives membrane repair?
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Resealing mechanism is dependent on size of membrane disruptionIncreasing size of membrane disruption
McNeil & Terasaki Nature Cell Biology 3, E124 - E129 (2001)
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Membrane tension is a key determinate of cell membrane resealing
Steinhardt Annals of the New York Academy of Sciences Vol 1066 pages 152–165, March 2006
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Evolution of fusion‐based resealing following development of endocytotic apparatus
McNeil & Terasaki Nature Cell Biology 3, E124 - E129 (2001)
A
B
C
D
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Skeletal muscle displays a substantial amount of membrane resealing
Organ Type of mechanical force Principal cells stressed
Cell wounding (proportion of cells involved)
Reference
Skeletal muscle Aperiodic, highly variable intensity: shear, stretch
Skeletal muscle cells (myocytes) Yes (3-20%) McNeil and Khakee,
1992
Cardiac muscle Cyclic: shear, stretch Cardiac myocytes Yes (25%) Clarke et al., 1995
SkinAperiodic, highly variable intensity: shear, stretch, compression
Epidermal cells, Fibroblasts, etc. Yes (3-6%) McNeil and Ito, 1990
Gastrointestinal tract Cyclic: shear, stretch Epithelial cells, smooth
muscle cells
Yes, epithelial cells (% not measured)
McNeil and Ito, 1989
Vascular (conducting) Constant and cyclic:shear Endothelial cells,
smooth muscle cells
Yes, aortic endothelial cells
(6.5%)Yu and McNeil, 1992
Respiratory Cyclic: stretchEpithelial cells, endotherlial cells, smooth muscle cells
Alveolar cells (2-30% in
mechanically ventilated lung)
Gajic et al., 2003
Peripheral nervous Aperiodic, highly variable intensity: shear Inner ear cells Yes, hair cells (%
not measured) Mulroy et al., 1998
McNeil and Steinhardt, Annu Rev Cell Dev Biol. 2003
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Contractile nature of skeletal muscles lead to extensive mechanical stress
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Topics for the class:What is cell membrane repair?
Why do cells need to actively repair their membranes?
How do cells repair the plasma membrane at the molecular level?
What are the pathologic consequences of defective membrane repair?
Can membrane repair be targeted as a therapeutic approach?
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Cellular mechanism are better understood than the molecular mechanisms
McNeil & KirchhausenNature Reviews Molecular Cell Biology 6, 499‐505 (June 2005)
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Dysferlin
McNeil & KirchhausenNature Reviews Molecular Cell Biology 6, 499‐505 (June 2005)
Originally determined to be a ferlin family protein that was known to be mutated inlimb girdle muscular dystrophy (type 2B) and Myoshi myopathy patients, (Nat Genet. 1998 Sep;20(1):31‐6).
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Muscular dystrophy and compromised membrane repair in dysferlin null mice
Bansal ,et al. Nature 423, 168‐172 (May 2003)
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Dysferlin function in membrane repair is not clear
Nat Clin Pract Cardiovascular Med (June 2005)
Molecular function of dysferlin in membrane repair is still not clear. Does it act asA fusogen for vesicles? Direct effects on remodeling of membrane? A platform to assemble other factors?
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Annexin‐A5 assembled into two‐dimensional arrays promotes cell membrane repair
Bouterm et al. Nature Communications 2, Article number: 270 doi:10.1038/ncomms1270
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AHNAK and other proteins interact with dysferlin and modulate membrane repair capacity
Huang, et al. March 2007 The FASEB Journal vol. 21 no. 3 732‐742
Multiple proteins have been shown to be important for the resealing of membranes, however the molecular function of these proteins is not clear.
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Other dysferlin interacting proteins linked to membrane repair
Wallace and McNally Annual Review of Physiology Vol. 71: 37‐57 (2009)
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Mitsugumin 53 (MG53) is a tripartite motif family protein linked to membrane trafficking during
membrane repair
82
40
MG53
Cai et al. Nature Cell Biology (2007)
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MG53 knockout mice display myopathy and breakdown of plasma membrane integrity
Cai et al. Nature Cell Biology (2007)
wt mg53-/-
200 µm
wt (3m) 50 µm mg53-/- (10m)mg53-/- (3m)
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MG53 is required for translocation of dysferlin to injury sites on the plasma membrane
Cai, Weisleder, et al. J Biol Chem. 2009 Jun 5;284(23):15894-902.
G
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MG53 also associated with dysferlin to facilitate membrane repair
Han (2011) Skeletal Muscle Vol. 1 Issue 1
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Proteins associated with vesicle fusion during endo/exocytosis are also involved in membrane repair
Andrews Sci. STKE, 3 May 2005 Vol. 2005, Issue 282, p. pe19
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Reorganization of the cytoskeleton and organelles is required for effective membrane repair
Mellgren. J Biol Chem. 2010 November 19; 285(47): 36597–36607.
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Topics for the class:What is cell membrane repair?
Why do cells need to actively repair their membranes?
How do cells repair the plasma membrane at the molecular level?
What are the pathologic consequences of defective membrane repair?
Can membrane repair be targeted as a therapeutic approach?
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Viral overexpression of target genes such as dysferlin
Grose, et al. PLoS One. 2012;7(6):e39233.
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Poloxamer 188 treatments
P.D.Chaudhari Pharmaceutical Information (2006) Vol. 4 Issue 3 http://www.maroonbiotech.com/
Poloxamer 188 is a long chain co‐block polymer that can increase membrane resealing following a number of different types of membrane damage.Has been shown to decrease dystrophic pathology in cardiac muscle.
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Weisleder, et al. Sci Transl Med. 2012 Jun 20;4(139):139ra85.
Recombinant MG53 (rhMG53) can locate to injury sites on the cell membrane
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Weisleder, et al. Sci Transl Med. 2012 Jun 20;4(139):139ra85.
rhMG53 can increase the resealing of muscle and non‐muscle cell membranes following various injuries
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Weisleder, et al. Sci Transl Med. 2012 Jun 20;4(139):139ra85.
Injection of rhMG53 can improve pathology in mdx model of muscular dystrophy
Saline rhMG53
mdx
mou
se 1
m
dxm
ouse
2
mdx
mou
se 3
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Potential mechanism for rhMG53 in membrane resealing
Alloush and Weisleder JAMA Neurology July 2013, Vol 70, No. 7