20 research outputs found
Quantum plasmonics: second-order coherence of surface plasmons launched by quantum emitters into a metallic film
We address the issue of the second-order coherence of single surface plasmons
launched by a quantum source of light into extended gold films. The quantum
source of light is made of a scanning fluorescent nanodiamond hosting five
nitrogen-vacancy (NV) color centers. By using a specially designed microscopy
that combines near-field optics with far-field leakage-radiation microscopy in
the Fourier space and adapted spatial filtering, we find that the quantum
statistics of the initial source of light is preserved after conversion to
surface plasmons and propagation along the polycrystalline gold film.Comment: Second version with minor changes made to comply with Referees'
comments. Editorially approved for publication in Phys. Rev. B on 22 June
201
Physiopathologie de la nephronophtise juvenile (identification de la nephrocystine-4 et caractérisation des partenaires protéiques des nephrocystines)
PARIS7-Bibliothèque centrale (751132105) / SudocSudocFranceF
Atteinte neurologique et syndrome néphrotique cortico-résistant
Les études génétiques portant sur le syndrome néphrotique (SN) héréditaire ont permis d’identifier plus de 60 gènes impliqués dans le développement de formes monogéniques de SN cortico-résistant, isolé ou syndromique, ce dernier étant parfois associé à des troubles neurologiques. Au cours des dernières décennies, diverses études ont établi des liens entre la physiologie des podocytes et celle des neurones, tant sur le plan morphologique (diaphragme de fente et synapse) que fonctionnel (plateformes de signalisation). Des variants dans des gènes codant des protéines s’exprimant dans différents compartiments du podocyte et des neurones sont responsables de phénotypes associant des lésions rénales avec protéinurie à des troubles neurologiques centraux et/ou périphériques. L’objectif de cette revue est de se concentrer sur les syndromes génétiques associant une protéinurie et une atteinte neurologique et de présenter les dernières avancées dans la description de ces troubles neuro-rénaux
Podocyte Purinergic P2X4 channels are mechanotransducers that mediate cytoskeletal disorganization
Podocytes are specialized, highly differentiated epithelial cells in the kidney glomerulus that are exposed to glomerular capillary pressure and possible increases in mechanical load. The proteins sensing mechanical forces in podocytes are unconfirmed, but the classic transient receptor potential channel 6 (TRPC6) interacting with the MEC-2 homolog podocin may form a mechanosensitive ion channel complex in podocytes. Here, we observed that podocytes respond to mechanical stimulation with increased intracellular calcium concentrations and increased inward cation currents. However, TRPC6-deficient podocytes responded in a manner similar to that of control podocytes, and mechanically induced currents were unaffected by genetic inactivation of TRPC1/3/6 or administration of the broad-range TRPC blocker SKF-96365. Instead, mechanically induced currents were significantly decreased by the specific P2X purinoceptor 4 (P2X(4)) blocker 5-BDBD. Moreover, mechanical P2X(4) channel activation depended on cholesterol and podocin and was inhibited by stabilization of the actin cytoskeleton. Because P2X(4) channels are not intrinsically mechanosensitive, we investigated whether podocytes release ATP upon mechanical stimulation using a fluorometric approach. Indeed, mechanically induced ATP release from podocytes was observed. Furthermore, 5-BDBD attenuated mechanically induced reorganization of the actin cytoskeleton. Altogether, our findings reveal a TRPC channel-independent role of P2X(4) channels as mechanotransducers in podocytes
C-terminal oligomerization of podocin mediates interallelic interactions
Interallelic interactions of membrane proteins are not taken into account while evaluating the pathogenicity of
sequence variants in autosomal recessive disorders. Podocin, a membrane-anchored component of the slit dia-
phragm, is encoded by NPHS2, the major gene mutated in hereditary podocytopathies. We formerly showed that
its R229Q variant is only pathogenic when trans-associated to specific 3′ mutations and suggested the causal role
of an abnormal C-terminal dimerization. Here we show by FRET analysis and size exclusion chromatography
that podocin oligomerization occurs exclusively through the C-terminal tail (residues 283–382): principally
through the first C-terminal helical region (H1, 283–313), which forms a coiled coil as shown by circular di-
chroism spectroscopy, and through the 332–348 region. We show the principal role of the oligomerization sites
in mediating interallelic interactions: while the monomer-forming R286Tfs*17 podocin remains membranous
irrespective of the coexpressed podocin variant identity, podocin variants with an intact H1 significantly in-
fluence each other's localization (r2 = 0.68, P = 9.2 × 10 −32). The dominant negative effect resulting in in-
tracellular retention of the pathogenic F344Lfs*4-R229Q heterooligomer occurs in parallel with a reduction in
the FRET efficiency, suggesting the causal role of a conformational rearrangement. On the other hand, oligo-
merization can also promote the membrane localization: it can prevent the endocytosis of F344Lfs*4 or F344*
podocin mutants induced by C-terminal truncation. In conclusion, C-terminal oligomerization of podocin can
mediate both a dominant negative effect and interallelic complementation. Interallelic interactions of NPHS2 are
not restricted to the R229Q variant and have to be considered in compound heterozygous individuals
P135: X-linked Alport syndrome: From transcriptomic diagnosis to preclinical assessment of splice-switching oligonucleotide therapy using patient-derived cells and kidney organoids*
Podocin Inactivation in Mature Kidneys Causes Focal Segmental Glomerulosclerosis and Nephrotic Syndrome
Podocin is a critical component of the glomerular slit diaphragm, and genetic mutations lead to both familial and sporadic forms of steroid-resistant nephrotic syndrome. In mice, constitutive absence of podocin leads to rapidly progressive renal disease characterized by mesangiolysis and/or mesangial sclerosis and nephrotic syndrome. Using established Cre-loxP technology, we inactivated podocin in the adult mouse kidney in a podocyte-specific manner. Progressive loss of podocin in the glomerulus recapitulated albuminuria, hypercholesterolemia, hypertension, and renal failure seen in nephrotic syndrome in humans. Lesions of FSGS appeared after 4 wk, with subsequent development of diffuse glomerulosclerosis and tubulointerstitial damage. Interestingly, conditional inactivation of podocin at birth resulted in a gradient of glomerular lesions, including mesangial proliferation, demonstrating a developmental stage dependence of renal histologic patterns of injury. The development of significant albuminuria in this model occurred only after early and focal foot process effacement had progressed to diffuse involvement, with complete absence of podocin immunolabeling at the slit diaphragm. Finally, we identified novel potential mediators and perturbed molecular pathways, including cellular proliferation, in the course of progression of renal disease leading to glomerulosclerosis, using global gene expression profiling
Podocyte Purinergic P2X 4
Podocytes are specialized, highly differentiated epithelial cells in the kidney glomerulus that are exposed to glomerular capillary pressure and possible increases in mechanical load. The proteins sensing mechanical forces in podocytes are unconfirmed, but the classic transient receptor potential channel 6 (TRPC6) interacting with the MEC-2 homolog podocin may form a mechanosensitive ion channel complex in podocytes. Here, we observed that podocytes respond to mechanical stimulation with increased intracellular calcium concentrations and increased inward cation currents. However, TRPC6-deficient podocytes responded in a manner similar to that of control podocytes, and mechanically induced currents were unaffected by genetic inactivation of TRPC1/3/6 or administration of the broad-range TRPC blocker SKF-96365. Instead, mechanically induced currents were significantly decreased by the specific P2X purinoceptor 4 (P2X(4)) blocker 5-BDBD. Moreover, mechanical P2X(4) channel activation depended on cholesterol and podocin and was inhibited by stabilization of the actin cytoskeleton. Because P2X(4) channels are not intrinsically mechanosensitive, we investigated whether podocytes release ATP upon mechanical stimulation using a fluorometric approach. Indeed, mechanically induced ATP release from podocytes was observed. Furthermore, 5-BDBD attenuated mechanically induced reorganization of the actin cytoskeleton. Altogether, our findings reveal a TRPC channel-independent role of P2X(4) channels as mechanotransducers in podocytes