Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2009-6-2
pubmed:abstractText
The tectorial membrane (TM) has a significantly larger stiffness in the radial direction than other directions, a prominent mechanical anisotropy that is believed to be critical for the proper functioning of the cochlea. To determine the molecular basis of this anisotropy, we measured material properties of TMs from mice with a targeted deletion of Col11a2, which encodes for collagen XI. In light micrographs, the density of TM radial collagen fibers was lower in Col11a2 -/- mice than wild-types. Tone-evoked distortion product otoacoustic emission and auditory brainstem response measurements in Col11a2 -/- mice were reduced by 30-50 dB independent of frequency as compared with wild-types, showing that the sensitivity loss is cochlear in origin. Stress-strain measurements made using osmotic pressure revealed no significant dependence of TM bulk compressibility on the presence of collagen XI. Charge measurements made by placing the TM as an electrical conduit between two baths revealed no change in the density of charge affixed to the TM matrix in Col11a2 -/- mice. Measurements of mechanical shear impedance revealed a 5.5 +/- 0.8 dB decrease in radial shear impedance and a 3.3 +/- 0.3 dB decrease in longitudinal shear impedance resulting from the Col11a2 deletion. The ratio of radial to longitudinal shear impedance fell from 1.8 +/- 0.7 for TMs from wild-type mice to 1.0 +/- 0.1 for those from Col11a2 -/- mice. These results show that the organization of collagen into radial fibrils is responsible for the mechanical anisotropy of the TM. This anisotropy can be attributed to increased mechanical coupling provided by the collagen fibrils. Mechanisms by which changes in TM material properties may contribute to the threshold elevation in Col11a2 -/- mice are discussed.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-10581026, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-10777727, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-10831863, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-12023228, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-12486177, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-12558277, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-12782348, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-12782349, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-15067120, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-15454468, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-1571955, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-15995703, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-16815909, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-16992076, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-17220887, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-17467292, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-17496047, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-17925447, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-18310237, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-18515382, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-213441, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-2460426, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-3542919, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-3821358, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-443008, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-7462465, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-7528739, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-8222646, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-8710939, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-9106521, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486694-9382104
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1542-0086
pubmed:author
pubmed:issnType
Electronic
pubmed:day
3
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4717-24
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Col11a2 deletion reveals the molecular basis for tectorial membrane mechanical anisotropy.
pubmed:affiliation
Harvard-MIT Division of Health Sciences and Technology and Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural