TY - JOUR
T1 - Plectin contributes to mechanical properties of living cells
AU - Na, Sungsoo
AU - Chowdhury, Farhan
AU - Tay, Bernard
AU - Ouyang, Mingxing
AU - Gregor, Martin
AU - Wang, Yingxiao
AU - Wiche, Gerhard
AU - Wang, Ning
PY - 2009/4
Y1 - 2009/4
N2 - Plectin is a 500-kDa cross-linking protein that plays important roles in a number of cell functions including migration and wound healing. We set out to characterize the role of plectin in mechanical properties of living cells. Plectin-/- cells were less stiff than plectin+/+ cells, but the slopes of the two power laws in response to loading frequencies (0.002-1,000 Hz) were similar. Plectin-/- cells lost the capacity to propagate mechanical stresses to long distances in the cytoplasm; traction forces in plectin-/- cells were only half of those in plectin +/+ cells, suggesting that plectin deficiency compromised prestress generation, which, in turn, resulted in the inhibition of long distance stress propagation. Both plectin+/+ and plectin-/- cells exhibited nonlinear stress-strain relationships. However, plectin+/+ cells, but not plectin -/- cells, further stiffened in response to lysophosphatidic acid (LPA). Dynamic fluorescence resonance energy transfer analysis revealed that RhoA GTPase proteins were activated in plectin +/+ cells but not in plectin-/- cells after treatment with LPA. Expression in plectin-/- cells of constitutively active RhoA (RhoA-V14) but not a dominant negative mutant of RhoA (RhoA-N19) or an empty vector restored the long distance force propagation behavior, suggesting that plectin is important in normal functions of RhoA. Our findings underscore the importance of plectin for mechanical properties, stress propagation, and prestress of living cells, thereby influencing their biological functions.
AB - Plectin is a 500-kDa cross-linking protein that plays important roles in a number of cell functions including migration and wound healing. We set out to characterize the role of plectin in mechanical properties of living cells. Plectin-/- cells were less stiff than plectin+/+ cells, but the slopes of the two power laws in response to loading frequencies (0.002-1,000 Hz) were similar. Plectin-/- cells lost the capacity to propagate mechanical stresses to long distances in the cytoplasm; traction forces in plectin-/- cells were only half of those in plectin +/+ cells, suggesting that plectin deficiency compromised prestress generation, which, in turn, resulted in the inhibition of long distance stress propagation. Both plectin+/+ and plectin-/- cells exhibited nonlinear stress-strain relationships. However, plectin+/+ cells, but not plectin -/- cells, further stiffened in response to lysophosphatidic acid (LPA). Dynamic fluorescence resonance energy transfer analysis revealed that RhoA GTPase proteins were activated in plectin +/+ cells but not in plectin-/- cells after treatment with LPA. Expression in plectin-/- cells of constitutively active RhoA (RhoA-V14) but not a dominant negative mutant of RhoA (RhoA-N19) or an empty vector restored the long distance force propagation behavior, suggesting that plectin is important in normal functions of RhoA. Our findings underscore the importance of plectin for mechanical properties, stress propagation, and prestress of living cells, thereby influencing their biological functions.
KW - Actin
KW - Mechanotransduction
KW - Prestress
KW - Stiffening
KW - Traction
UR - http://www.scopus.com/inward/record.url?scp=65649130513&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=65649130513&partnerID=8YFLogxK
U2 - 10.1152/ajpcell.00604.2008
DO - 10.1152/ajpcell.00604.2008
M3 - Article
C2 - 19244477
AN - SCOPUS:65649130513
SN - 0363-6143
VL - 296
SP - C868-C877
JO - American Journal of Physiology - Cell Physiology
JF - American Journal of Physiology - Cell Physiology
IS - 4
ER -