Difference between revisions of "Guerrero 2010 Mol Cell Biochem"
Bader Helga (talk | contribs) |
Bader Helga (talk | contribs) |
||
Line 1: | Line 1: | ||
{{Publication | {{Publication | ||
|title=Guerrero K, Monge C, Brückner A, Puurand U, Kadaja L, Käämbre T, Seppet E, Saks V ( | |title=Guerrero K, Monge C, Brückner A, Puurand U, Kadaja L, Käämbre T, Seppet E, Saks V (2010) Study of possible interactions of tubulin, microtubular network, and STOP protein with mitochondria in muscle cells. Mol Cell Biochem 337:239-49. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/19888554 PMID: 19888554] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/19888554 PMID: 19888554] | ||
|authors=Guerrero K, Monge C, Brueckner A, Puurand U, Kadaja L, Kaeaembre T, Seppet E, Saks V | |authors=Guerrero K, Monge C, Brueckner A, Puurand U, Kadaja L, Kaeaembre T, Seppet E, Saks V | ||
|year= | |year=2010 | ||
|journal=Mol Cell Biochem | |journal=Mol Cell Biochem | ||
|abstract=We studied possible connections of tubulin, microtubular system, and microtubular network stabilizing STOP protein with mitochondria in rat and mouse cardiac and skeletal muscles by confocal microscopy and oxygraphy. Intracellular localization and content of tubulin was found to be muscle type-specific, with high amounts in oxidative muscles, and much lower in glycolytic skeletal muscle. STOP protein localization and content in muscle cells was also muscle type-specific. In isolated heart mitochondria, addition of 1 μM tubulin heterodimer increased apparent K<sub>m</sub> for ADP significantly. Dissociation of microtubular system into free tubulin by colchicine treatment only slightly decreased initially high apparent K<sub>m</sub> for ADP in permeabilized cells, and diffusely distributed free tubulin stayed inside the cells, obviously connected to the intracellular structures. To identify the genes that are specific for oxidative muscle, we developed and applied a method of kindred DNA. The results of sequencing and bioinformatic analysis of isolated cDNA pool common for heart and ''m. soleus'' showed that in adult mice the β-tubulin gene is expressed predominantly in oxidative muscle cells. It is concluded that whereas dimeric tubulin may play a significant role in regulation of mitochondrial outer membrane permeability in the cells ''in vivo'', its organization into microtubular network has a minor significance on that process. | |abstract=We studied possible connections of tubulin, microtubular system, and microtubular network stabilizing STOP protein with mitochondria in rat and mouse cardiac and skeletal muscles by confocal microscopy and oxygraphy. Intracellular localization and content of tubulin was found to be muscle type-specific, with high amounts in oxidative muscles, and much lower in glycolytic skeletal muscle. STOP protein localization and content in muscle cells was also muscle type-specific. In isolated heart mitochondria, addition of 1 μM tubulin heterodimer increased apparent K<sub>m</sub> for ADP significantly. Dissociation of microtubular system into free tubulin by colchicine treatment only slightly decreased initially high apparent K<sub>m</sub> for ADP in permeabilized cells, and diffusely distributed free tubulin stayed inside the cells, obviously connected to the intracellular structures. To identify the genes that are specific for oxidative muscle, we developed and applied a method of kindred DNA. The results of sequencing and bioinformatic analysis of isolated cDNA pool common for heart and ''m. soleus'' showed that in adult mice the β-tubulin gene is expressed predominantly in oxidative muscle cells. It is concluded that whereas dimeric tubulin may play a significant role in regulation of mitochondrial outer membrane permeability in the cells ''in vivo'', its organization into microtubular network has a minor significance on that process. | ||
|keywords=Cytoskeleton, | |keywords=Cytoskeleton, Mitochondria, Oxidative phosphorylation, Tubulin, Microtubular Network, STOP protein, Heart, Skeletal muscles | ||
|mipnetlab=EE Tallinn Saks VA, FR Grenoble Saks VA, EE Tartu Seppet EK | |mipnetlab=EE Tallinn Saks VA, FR Grenoble Saks VA, EE Tartu Seppet EK | ||
|discipline=Mitochondrial Physiology | |discipline=Mitochondrial Physiology |
Revision as of 13:47, 20 May 2015
Guerrero K, Monge C, Brückner A, Puurand U, Kadaja L, Käämbre T, Seppet E, Saks V (2010) Study of possible interactions of tubulin, microtubular network, and STOP protein with mitochondria in muscle cells. Mol Cell Biochem 337:239-49. |
Guerrero K, Monge C, Brueckner A, Puurand U, Kadaja L, Kaeaembre T, Seppet E, Saks V (2010) Mol Cell Biochem
Abstract: We studied possible connections of tubulin, microtubular system, and microtubular network stabilizing STOP protein with mitochondria in rat and mouse cardiac and skeletal muscles by confocal microscopy and oxygraphy. Intracellular localization and content of tubulin was found to be muscle type-specific, with high amounts in oxidative muscles, and much lower in glycolytic skeletal muscle. STOP protein localization and content in muscle cells was also muscle type-specific. In isolated heart mitochondria, addition of 1 μM tubulin heterodimer increased apparent Km for ADP significantly. Dissociation of microtubular system into free tubulin by colchicine treatment only slightly decreased initially high apparent Km for ADP in permeabilized cells, and diffusely distributed free tubulin stayed inside the cells, obviously connected to the intracellular structures. To identify the genes that are specific for oxidative muscle, we developed and applied a method of kindred DNA. The results of sequencing and bioinformatic analysis of isolated cDNA pool common for heart and m. soleus showed that in adult mice the β-tubulin gene is expressed predominantly in oxidative muscle cells. It is concluded that whereas dimeric tubulin may play a significant role in regulation of mitochondrial outer membrane permeability in the cells in vivo, its organization into microtubular network has a minor significance on that process. • Keywords: Cytoskeleton, Mitochondria, Oxidative phosphorylation, Tubulin, Microtubular Network, STOP protein, Heart, Skeletal muscles
• O2k-Network Lab: EE Tallinn Saks VA, FR Grenoble Saks VA, EE Tartu Seppet EK
Labels: MiParea: Respiration, Genetic knockout;overexpression
Organism: Mouse, Rat
Tissue;cell: Heart, Skeletal muscle
Preparation: Permeabilized cells, Isolated mitochondria
Regulation: ADP, PCr;Cr Coupling state: OXPHOS
HRR: Oxygraph-2k