Literature DB >> 8402956

Expression of four myosin heavy chain isoforms with development in mouse uterus.

T J Eddinger1, J A Wolf.   

Abstract

In smooth muscle tissue, two or three isoforms of myosin heavy chain (MHC) have been reported (SM1, SM2, and/or NM). In mouse uterus tissue, four bands in the region of the MHC's can be resolved on high resolution SDS polyacrylamide gels. Western blots using smooth muscle (SM) MHC-specific and nonmuscle (NM) MHC-specific polyclonal antibodies show the upper two bands in the MHC region are SM isoforms, whereas the lower two bands are NM isoforms. One-dimensional peptide maps of these four bands show each to have a unique pattern of polypeptide fragments following alpha-chymotrypsin digestion. Developmental expression of myosin heavy chains (MHC) in mouse uterus, aorta, bladder, and stomach (6 ages, 10-150 days) was determined using tissue homogenates. In the uterus, both SM MHC's show an increase in relative content with increasing age, whereas the NM MHC's show a decrease. The mouse aorta shows a significant increase in the SM MHC's and a significant decrease in the NM MHC from day 10 to day 30, which is similar to data reported for the rat aorta. Whereas both the bladder and stomach contain relatively small amounts of NM MHC's (approximately 10% or less), these quantities do show decreases with development. The SM1:SM2 ratio for the uterus remains high (3.4 at 150 days) through development; the aorta, bladder, and stomach also start out high, but tend toward 1.0 in the 150-day animals. The presence of four MHC isoforms in the uterus with unique developmental regulation of expression is consistent with hypotheses of unique functional roles for these isoforms.

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Year:  1993        PMID: 8402956     DOI: 10.1002/cm.970250406

Source DB:  PubMed          Journal:  Cell Motil Cytoskeleton        ISSN: 0886-1544


  10 in total

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2.  Small intestinal submucosa seeded with intestinal smooth muscle cells in a rodent jejunal interposition model.

Authors:  Harry H Qin; James C Y Dunn
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3.  Nonmuscle myosin, force maintenance, and the tonic contractile phenotype in smooth muscle.

Authors:  Albert Y Rhee; Ozgur Ogut; Frank V Brozovich
Journal:  Pflugers Arch       Date:  2006-05-10       Impact factor: 3.657

Review 4.  Myosin isoforms in smooth muscle: how may they affect function and structure?

Authors:  A P Somlyo
Journal:  J Muscle Res Cell Motil       Date:  1993-12       Impact factor: 2.698

5.  Telokin expression is restricted to smooth muscle tissues during mouse development.

Authors:  B P Herring; G E Lyons; A M Hoggatt; P J Gallagher
Journal:  Am J Physiol Cell Physiol       Date:  2001-01       Impact factor: 4.249

Review 6.  Regulation of the smooth muscle contractile phenotype by nonmuscle myosin.

Authors:  Ozgur Ogut; Samantha L Yuen; Frank V Brozovich
Journal:  J Muscle Res Cell Motil       Date:  2008-03-18       Impact factor: 2.698

7.  TLRR (lrrc67) interacts with PP1 and is associated with a cytoskeletal complex in the testis.

Authors:  Rong Wang; Aseem Kaul; Ann O Sperry
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8.  SMB myosin heavy chain knockout enhances tonic contraction and reduces the rate of force generation in ileum and stomach antrum.

Authors:  Qian Huang; Gopal J Babu; Muthu Periasamy; Thomas J Eddinger
Journal:  Am J Physiol Cell Physiol       Date:  2012-11-07       Impact factor: 4.249

9.  The carboxyl-terminal isoforms of smooth muscle myosin heavy chain determine thick filament assembly properties.

Authors:  Arthur S Rovner; Patricia M Fagnant; Susan Lowey; Kathleen M Trybus
Journal:  J Cell Biol       Date:  2002-01-07       Impact factor: 10.539

10.  Tonic and phasic smooth muscle contraction is not regulated by the PKCα - CPI-17 pathway in swine stomach antrum and fundus.

Authors:  Yu Zhang; Meghan E Hermanson; Thomas J Eddinger
Journal:  PLoS One       Date:  2013-09-18       Impact factor: 3.240

  10 in total

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