Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1998-2-10
pubmed:abstractText
Phosphorylation of the regulatory light chain of myosin II (RMLC) at Serine 19 by a specific enzyme, MLC kinase, is believed to control the contractility of actomyosin in smooth muscle and vertebrate nonmuscle cells. To examine how such phosphorylation is regulated in space and time within cells during coordinated cell movements, including cell locomotion and cell division, we generated a phosphorylation-specific antibody. Motile fibroblasts with a polarized cell shape exhibit a bimodal distribution of phosphorylated myosin along the direction of cell movement. The level of myosin phosphorylation is high in an anterior region near membrane ruffles, as well as in a posterior region containing the nucleus, suggesting that the contractility of both ends is involved in cell locomotion. Phosphorylated myosin is also concentrated in cortical microfilament bundles, indicating that cortical filaments are under tension. The enrichment of phosphorylated myosin in the moving edge is shared with an epithelial cell sheet; peripheral microfilament bundles at the leading edge contain a higher level of phosphorylated myosin. On the other hand, the phosphorylation level of circumferential microfilament bundles in cell-cell contacts is low. These observations suggest that peripheral microfilaments at the edge are involved in force production to drive the cell margin forward while microfilaments in cell-cell contacts play a structural role. During cell division, both fibroblastic and epithelial cells exhibit an increased level of myosin phosphorylation upon cytokinesis, which is consistent with our previous biochemical study (Yamakita, Y., S. Yamashiro, and F. Matsumura. 1994. J. Cell Biol. 124:129-137). In the case of the NRK epithelial cells, phosphorylated myosin first appears in the midzones of the separating chromosomes during late anaphase, but apparently before the formation of cleavage furrows, suggesting that phosphorylation of RMLC is an initial signal for cytokinesis.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-1421576, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-1826467, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-1854490, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-1955473, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-2519609, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-2692841, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-2988424, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-3060469, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-3305021, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-3525577, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-3525578, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-5485752, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-62755, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-7622562, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-7691416, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-7806558, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-7806572, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8081830, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8167030, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8188629, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8226923, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8266074, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8294496, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8388877, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8436590, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8486737, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8522610, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8590803, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8662509, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8702756, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8707847, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-8856669, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-9013669, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-9096954, http://linkedlifedata.com/resource/pubmed/commentcorrection/9425160-9139666
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0021-9525
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
140
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
119-29
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
Specific localization of serine 19 phosphorylated myosin II during cell locomotion and mitosis of cultured cells.
pubmed:affiliation
Department of Molecular Biology and Biochemistry, Rutgers University, Nelson Labs, Busch Campus, Piscataway, New Jersey 08855, USA. Matsumura@mbcl.rutgers.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't