LEONARDO YUJI TANAKA

(Fonte: Lattes)
Índice h a partir de 2011
12
Projetos de Pesquisa
Unidades Organizacionais
Instituto do Coração, Hospital das Clínicas, Faculdade de Medicina
LIM/64, Hospital das Clínicas, Faculdade de Medicina - Líder

Resultados de Busca

Agora exibindo 1 - 4 de 4
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    Early exposure to high-sucrose diet triggers hippocampal endoplasmic reticulum-stress in young rats
    (2016) PAES, Antonio Marcus de Andrade; PINTO, Bruno Araujo Serra; MELO, Thamys Marinho; FLISTER, Karla Frida Torres; FRANCA, Lucas Martins; TANAKA, Leonardo Yudi; LAURINDO, Francisco Rafael Martins
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    Peri/epicellular protein disulfide isomerase PDI acts as an organizer of cytoskeletal mechanoadaptation in vascular smooth muscle cells
    (2018) TANAKA, Leonardo Yuji; ARAUJO, Thais Larissa; RODRIGUEZ, Andres Ignacio; FERRAZ, Mariana Sacrini Ayres; PELEGATI, Vitor Bianchin; SANTOS, Aline Mara; CESAR, Carlos Lens; ALENCAR, Adriano Mesquita; LAURINDO, Francisco Rafael Martins
  • conferenceObject
    Early exposure to high-sucrose diet triggers hippocampal endoplasmic reticulum-stress in young rats
    (2016) PAES, Antonio Marcus de Andrade; PINTO, Bruno Araujo Serra; MELO, Thamys Marinho; FLISTER, Karla Frida Torres; FRANCA, Lucas Martins; TANAKA, Leonardo Yudi; LAURINDO, Francisco Rafael Martins
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    Role of Protein Disulfide Isomerase during vascular repair after injury
    (2012) TANAKA, Leonardo Yuji; ARAUJO, Haniel Alves; CSORDAS, Andre Alcantara; HIRONAKA, Gustavo Ken; TAKIMURA, Celso Kiyochi; LAURINDO, Francisco Rafael Martins
    Endoplasmic reticulum(ER) redox chaperone protein disulfide isomerase(PDI) regulates vascular/phagocytic NADPH oxidase and supports cell migration. We investigated the role of PDI during vascular repair after injury(AI) induced by balloon in rabbit iliac artery. There was marked increase of PDI mRNA and protein(5–10-fold) at 4, 7 and 14 days AI vs. intact control(CT). PDI immunostaining was greater in intima = neo-endothelium > media. Increased cell-surface PDI was also evident. ER stress-related KDEL chaperones also increased with similar time-course AI. PDI siRNA(siPDI) transfection in cultured vessel rings collected 14 days AI enhanced KDEL expression vs. scrambled siRNA(siScr) (siScr 2.1±0.9 vs. siPDI 5.0±2.3-fold vs. CT, p<0.05), apoptosis (siScr 4.6±0.2 vs. siPDI 6.2±0.9 %TUNEL + nuclei, p<0.05) and proliferation marker PCNA (siScr 1.2±0.3 vs. siPDI 4.0 ±0.2 AU, p<0.05), and decreased differentiation marker calponin-C (siScr 0.52±0.04 vs. siPDI 0.36 ±0.04 AU, p<0.05). siPDI in CT rings did not alter such variables. PCR array analysis showed analogous pattern of mRNA changes. Also, siPDI 14 days AI upregulated Nox1 and downregulated Nox4 NADPH oxidase, while siPDI attenuated oxidant production (in situ hydroethidine) only in CT vessels. Thus, strongly-overexpressed PDI 14 days AI protects against apoptosis and ER stress and sustains VSMC differentiation.