TY - JOUR
T1 - Tissue specific characterisation of Lim-kinase 1 expression during mouse embryogenesis
AU - Lindström, Nils O.
AU - Neves, Carlos
AU - McIntosh, Rebecca
AU - Miedzybrodzka, Zosia
AU - Vargesson, Neil
AU - Martin Collinson, J.
N1 - Funding Information:
This work was funded by the Medical Research Council (UK) (Grant award: G0800901 ).
PY - 2011/3
Y1 - 2011/3
N2 - The Lim-kinase (LIMK) proteins are important for the regulation of the actin cytoskeleton, in particular the control of actin nucleation and depolymerisation via regulation of cofilin, and hence may control a large number of processes during development, including cell tensegrity, migration, cell cycling, and axon guidance. LIMK1/LIMK2 knockouts disrupt spinal cord morphogenesis and synapse formation but other tissues and developmental processes that require LIMK are yet to be fully determined. To identify tissues and cell-types that may require LIMK, we characterised the pattern of LIMK1 protein during mouse embryogenesis. We showed that LIMK1 displays an expression pattern that is temporally dynamic and tissue-specific. In several tissues LIMK1 is detected in cell-types that also express Wilms' tumour protein 1 and that undergo transitions between epithelial and mesenchymal states, including the pleura, epicardium, kidney nephrons, and gonads. LIMK1 was also found in a subset of cells in the dorsal retina, and in mesenchymal cells surrounding the peripheral nerves. This detailed study of the spatial and temporal expression of LIMK1 shows that LIMK1 expression is more dynamic than previously reported, in particular at sites of tissue-tissue interactions guiding multiple developmental processes.
AB - The Lim-kinase (LIMK) proteins are important for the regulation of the actin cytoskeleton, in particular the control of actin nucleation and depolymerisation via regulation of cofilin, and hence may control a large number of processes during development, including cell tensegrity, migration, cell cycling, and axon guidance. LIMK1/LIMK2 knockouts disrupt spinal cord morphogenesis and synapse formation but other tissues and developmental processes that require LIMK are yet to be fully determined. To identify tissues and cell-types that may require LIMK, we characterised the pattern of LIMK1 protein during mouse embryogenesis. We showed that LIMK1 displays an expression pattern that is temporally dynamic and tissue-specific. In several tissues LIMK1 is detected in cell-types that also express Wilms' tumour protein 1 and that undergo transitions between epithelial and mesenchymal states, including the pleura, epicardium, kidney nephrons, and gonads. LIMK1 was also found in a subset of cells in the dorsal retina, and in mesenchymal cells surrounding the peripheral nerves. This detailed study of the spatial and temporal expression of LIMK1 shows that LIMK1 expression is more dynamic than previously reported, in particular at sites of tissue-tissue interactions guiding multiple developmental processes.
KW - Epithelia-to-mesenchyme transition
KW - Eye
KW - Heart
KW - Kidney
KW - Limk
KW - Mesenchyme-to- epithelia transition
KW - Testes
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U2 - 10.1016/j.gep.2010.12.003
DO - 10.1016/j.gep.2010.12.003
M3 - Article
C2 - 21167960
AN - SCOPUS:79953056392
VL - 11
SP - 221
EP - 232
JO - Brain research. Gene expression patterns
JF - Brain research. Gene expression patterns
SN - 1567-133X
IS - 3-4
ER -