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1 ordia within the mesonephric (embryonic) and metanephric (adult) kidneys and the Mullerian duct, the
2 e group reported the intriguing finding that metanephric allografts and congenic, major histocompatib
4 ein level is sufficient for establishing the metanephric blastema and inducing the ureteric bud forma
6 mal interaction between the ureteral bud and metanephric blastema leads to renal hypodysplasia, vesic
8 ed here demonstrate that Eya 1 specifies the metanephric blastema within the intermediate mesoderm at
9 aintenance/growth and differentiation of the metanephric blastema, and constitutively activated STATs
14 tisense-oligodeoxynucleotide or -antibody in metanephric culture induced dysmorphogenesis of the kidn
16 For further testing of the role of CFTR, metanephric cultures were prepared from mice with a targ
17 C chemokines and their receptor CXCR2 during metanephric development and suggest a novel mechanism fo
20 mpared with the primate kidney, and abnormal metanephric development in culture in the absence of bet
21 eteric bud formation at the initial stage of metanephric development in most Gdf11 mutant embryos exa
23 R2, were expressed at the earliest stages of metanephric development in the rat, and signaling throug
26 lized to somites and neural tube, and during metanephric development predominantly to the ureteric bu
28 genes corresponding to the earliest stage of metanephric development, and underexpressed genes corres
30 for cell survival and proliferation in early metanephric development, whereas others, including SIX1,
36 pport a model where Hox11 paralogs specify a metanephric developmental program in responsive intermed
37 ractions, its deficiency may have led to the metanephric dysmorphogenesis and consequential atrophy o
40 in human organogenesis; on the basis of the metanephric expression pattern, the results suggest that
41 plays a central role in the specification of metanephric fate and in the maintenance of metanephric m
42 a critical determination factor in acquiring metanephric fate within the intermediate mesoderm and as
44 he phosphotyrosine kinase domains, inhibited metanephric growth in the organ culture; the most dramat
45 on of nephric duct elongation and failure of metanephric induction in the Odd 1(-/-) mutant embryos.
46 ype demonstrates that Hox11 control of early metanephric induction is accomplished by the interaction
47 nf-Ret signal transduction pathway initiates metanephric induction, no single regulator has yet been
52 chymal precursors within the mesonephric and metanephric kidney and is subsequently downregulated upo
54 e that the majority of cell types within the metanephric kidney arise from an Osr1(+) population of m
56 SCF elicits growth-promoting effects in the metanephric kidney by expanding one or more components o
60 cid following the teratogenic insult rescued metanephric kidney development and abrogated several ext
61 intermediate mesoderm, the earliest step of metanephric kidney development and the molecular mechani
62 ial structures, especially the notochord, in metanephric kidney development has not been directly exa
66 During fetal development, nephrons of the metanephric kidney form from a mesenchymal progenitor po
67 t express several other factors required for metanephric kidney formation, including Eya1, Six2, Pax2
69 (20% O2) or low oxygen (1-3% O2) conditions, metanephric kidney growth and morphology were assessed b
70 6 d in culture in serum-free, defined media, metanephric kidney growth and morphology were assessed.
76 e Wolffian duct (WD), the initiating step in metanephric kidney morphogenesis, is dependent on GDNF;
78 de new insights into the cellular origins of metanephric kidney structures and lend support to a mode
80 nchyme regulates growth and branching in the metanephric kidney through the local regulation of urete
82 ud epithelia during early development of the metanephric kidney, and disruption of the PKD1 gene in m
83 s mutants are born with abnormalities of the metanephric kidney, including duplex kidneys and double
84 ll states that accompany the assembly of the metanephric kidney, likely reflecting diverse regulatory
86 u hybridizations with Wnt7b, a marker of the metanephric kidney, show that the branching defect was n
87 bud (UB) is critical for development of the metanephric kidney, the specific patterns of branching a
95 the developing kidney vasculature, avascular metanephric kidneys from rat embryos (E14) were cocultur
97 ureteric bud lumen of embryonic day 11 mouse metanephric kidneys resulted in disrupted branching morp
99 nder defined conditions in organ cultures of metanephric kidneys, c-kit-positive cells, including the
100 exhibit complete agenesis of adrenal glands, metanephric kidneys, gonads, and defects in pericardium
101 s, since Wnt4 knockout mice, which also lack metanephric kidneys, show normal expression of Myh7, Myl
108 ted by a coordinated reciprocal induction of metanephric mesenchymal (MM) and ureteric bud (UB) cells
109 f Wnt signaling leads to profound changes in metanephric mesenchymal cell morphology, including disru
111 unostaining is evident on a subpopulation of metanephric mesenchymal cells and on putative progenitor
112 involvement in PDGF-induced DNA synthesis in metanephric mesenchymal cells and provides the first evi
114 d explored the biological effects of PDGF in metanephric mesenchymal cells in an attempt to determine
117 GF stimulates proliferation and migration of metanephric mesenchymal cells, from which mesangial cell
120 tion utilizing an organ culture model of rat metanephric mesenchymal differentiation, which recapitul
123 ular transformation of primary rat embryonic metanephric mesenchymal precursor cells (MM cells) by KS
124 t maintain the undifferentiated state of the metanephric mesenchymal precursor cells have not yet bee
125 ne the role of Wnt signaling, we treated rat metanephric mesenchymal progenitors directly with recomb
131 canonical Wnt signaling is not activated in metanephric mesenchyme (MM) during its conversion to the
132 neage tracing studies suggest that condensed metanephric mesenchyme (MM) gives rise to nephronic epit
137 owth factor receptors (Fgfrs) 1 and 2 in the metanephric mesenchyme (MM) of mice leads to a virtual a
139 dneys, aberrant cell death occurs within the metanephric mesenchyme (MM), particularly in the cortica
140 s likely due to a defect in induction of the metanephric mesenchyme (MM), which along with the ureter
144 sis of the ureteric bud (UB) [induced by the metanephric mesenchyme (MM)] is necessary for normal kid
146 nt and in response to inductive signals, the metanephric mesenchyme aggregates, becomes polarized, an
147 5 results in improper differentiation of the metanephric mesenchyme and absence of essential developm
151 cell line thought to originate in the early metanephric mesenchyme and glial cell line-derived neuro
152 signaling molecule GDNF is expressed in the metanephric mesenchyme and has recently been implicated
153 hat PDGFR beta localizes to undifferentiated metanephric mesenchyme and is later expressed in the cle
154 e enriched in the ureteric bud compared with metanephric mesenchyme and predicted to code for secrete
155 pment have considered the interaction of the metanephric mesenchyme and the ureteric bud to be the ma
156 ined its ability both to promote survival of metanephric mesenchyme and to induce nephrogenesis in cu
158 teractions between the ureteric bud (UB) and metanephric mesenchyme are crucial for tubulogenesis dur
159 ractions between the ureteric epithelium and metanephric mesenchyme are essential for kidney morphoge
160 ions between the ureteric epithelium and the metanephric mesenchyme are needed to drive growth and di
161 dicate that Sall1-dependent signals from the metanephric mesenchyme are required to modulate ureteric
162 s between the embryonic ureteric bud and the metanephric mesenchyme are the basis for kidney developm
163 g kidney, Six1 is expressed in the uninduced metanephric mesenchyme at E10.5 and in the induced mesen
164 Eya1 expression was unaffected in Six1(-/-) metanephric mesenchyme at E10.5, indicating that Eya1 ma
165 Sall1 expression was markedly reduced in the metanephric mesenchyme at E10.5, indicating that Six1 is
166 a8 integrin-null mutants specifically in the metanephric mesenchyme at the time of ureteric bud invas
168 be traced to a delay in the invasion of the metanephric mesenchyme by the ureteric bud at an early s
169 ble factor(s) in the conditioned medium of a metanephric mesenchyme cell line is essential for multip
170 eiotrophin, from the conditioned medium of a metanephric mesenchyme cell line that induces isolated u
174 8 gene is expressed together with Hoxa 11 in metanephric mesenchyme cells, and mutation of Integrin a
175 Osr1, Eya1, Pax2 or Wt1 gene function in the metanephric mesenchyme compromises the formation of the
177 As a result of this induction, most of the metanephric mesenchyme converts into epithelium of a nep
179 In the embryonic kidney, progenitors in the metanephric mesenchyme differentiate into specialized re
181 onship between Pax, Eya and Six genes in the metanephric mesenchyme during early kidney development i
184 me and proper demarcation of mesonephric and metanephric mesenchyme from the WD depends on RetY1015 s
185 nd/or miRNAPG mutations show a pre-induction metanephric mesenchyme gene expression pattern and are s
186 vitro and in vivo, a fraction of the induced metanephric mesenchyme in Cad-6 mutant kidneys fails to
187 During kidney development, factors from the metanephric mesenchyme induce the growth and repeated br
188 the subsequent invasion of the bud into the metanephric mesenchyme initiate the process of metanephr
191 We demonstrate that Pax2 expression in the metanephric mesenchyme is independent of induction by th
192 egrin, invasion by the ureteric bud into the metanephric mesenchyme is inhibited, resulting in renal
194 ow that both Eya1 and Six1 expression in the metanephric mesenchyme is preserved in Pax2(-/-) embryos
195 between the branching ureteric buds and the metanephric mesenchyme lead to mesenchyme-to-epithelium
196 he overexpression of beta-catenin within the metanephric mesenchyme leads to ectopic and disorganized
197 Second, beta-catenin overexpression in the metanephric mesenchyme leads to elevated levels of trans
198 inactivation of p53 in the UB but not in the metanephric mesenchyme lineage recapitulated the duplex
202 lator has yet been identified to specify the metanephric mesenchyme or blastema within the intermedia
203 e or together with Bmp7) maintained isolated metanephric mesenchyme or sorted nephron progenitors tha
204 f metanephric fate and in the maintenance of metanephric mesenchyme proliferation and survival by act
205 n which the elevation of beta-catenin in the metanephric mesenchyme results in cell-autonomous and no
206 ent in a conditioned medium derived from the metanephric mesenchyme that supports non-branching growt
207 etween the ureteric bud epithelium, inducing metanephric mesenchyme to differentiate into nephrons, a
210 for the normal nephrogenesis response of the metanephric mesenchyme to inductive signals from the ure
212 renal collecting system induces surrounding metanephric mesenchyme to proliferate and differentiate
213 k by antagonizing inductive signals from the metanephric mesenchyme to the illegitimate sites on the
216 f8 expression was reduced in early-stage DKO metanephric mesenchyme, accompanied by reduced levels of
217 It is believed that Gdnf, produced in the metanephric mesenchyme, activates Ret signaling in the W
218 ity preferentially in epithelia derived from metanephric mesenchyme, and defects in kidney architectu
220 posterior intermediate mesodermal cells, the metanephric mesenchyme, and induces the formation of the
221 prouty1 and WT1 overlapped in the developing metanephric mesenchyme, and Sprouty1, like WT1, plays a
222 lling is not active in the early nephrogenic metanephric mesenchyme, but instead provide expressional
223 , the ureteric bud grows out and invades the metanephric mesenchyme, but it fails to initiate branchi
224 bryos by specifically expressing Six1 in the metanephric mesenchyme, but not the ureter, under contro
226 Despite the restricted expression of Pbx1 in metanephric mesenchyme, developing nephrons, and stroma,
227 survival factors (EGF, bFGF) and inducers of metanephric mesenchyme, including the ureteric bud, spin
228 senchyme to differentiate into nephrons, and metanephric mesenchyme, inducing the ureteric bud to gro
229 ells interact with the adjacent cells of the metanephric mesenchyme, inducing their conversion into n
230 oligonucleotides reduced condensation of the metanephric mesenchyme, leading to a decreased number of
231 phric capillaries express Tie genes, whereas metanephric mesenchyme, maturing tubules, and mature pod
232 ured UB was recombined with freshly isolated metanephric mesenchyme, nephric units were induced in th
233 both DLG1 and CASK either 1) globally, 2) in metanephric mesenchyme, or 3) in nephron progenitors.
234 human embryos, OFD1a immunolocalized to the metanephric mesenchyme, oral mucosa, nasal and cranial c
235 clusters of epithelial progenitors from the metanephric mesenchyme, thereby separating them from the
236 owth factor receptors (fgfrs) 1 and 2 in the metanephric mesenchyme, we generated conditional knockou
237 by isolating epithelial progenitors from the metanephric mesenchyme, we show that they are targeted b
238 are thought to play an important role in the metanephric mesenchyme, when cells aggregate to form the
239 ficient to trigger tubulogenesis in isolated metanephric mesenchyme, whereas Wnt-11 which is expresse
240 ney, the epithelial ureteric bud invades the metanephric mesenchyme, which directs the ureteric bud t
241 its effects on the adjacent ureteric bud and metanephric mesenchyme, which fail to grow and different
242 Hoxa11 expression is restricted to the early metanephric mesenchyme, which induces ureteric bud forma
243 een the epithelial ureteric bud and adjacent metanephric mesenchyme, which is induced by the bud to f
278 ng molecules, we developed an assay in which metanephric mesenchymes are rescued from apoptosis by fa
280 the mutual induction of the ureteric bud and metanephric mesoderm, whereas the malpighian tubules of
285 ant human VEGF (5 ng/ml) was examined on rat metanephric organ culture, a model known to recapitulate
286 we examined the effect of low oxygen on rat metanephric organ culture, a model known to recapitulate
295 exposure to excess retinoic acid well before metanephric rudiments exist leads to failure of kidney f
296 t an altered morphology and activate several metanephric specific markers normally confined to distal
297 s tubule forming progenitors and instructs a metanephric specific pattern of nephron differentiation.
300 ntial for the development of mesonephric and metanephric tubules and caudal extension of the Mulleria
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