Verônica M. Saia‐Cereda

ORCID: 0000-0002-6285-1201
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Research Areas
  • Advanced Proteomics Techniques and Applications
  • Cellular transport and secretion
  • Epigenetics and DNA Methylation
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Long-Term Effects of COVID-19
  • Neurogenesis and neuroplasticity mechanisms
  • 14-3-3 protein interactions
  • Metabolomics and Mass Spectrometry Studies
  • Tryptophan and brain disorders
  • Neuroscience and Neuropharmacology Research
  • Receptor Mechanisms and Signaling
  • Mass Spectrometry Techniques and Applications
  • RNA Research and Splicing
  • COVID-19 Clinical Research Studies
  • Diet and metabolism studies
  • Glycosylation and Glycoproteins Research
  • Pluripotent Stem Cells Research
  • COVID-19 and Mental Health
  • Wnt/β-catenin signaling in development and cancer
  • Neuropeptides and Animal Physiology
  • Sirtuins and Resveratrol in Medicine
  • Neuroscience and Neural Engineering
  • Neurological disorders and treatments
  • Bipolar Disorder and Treatment
  • Bioinformatics and Genomic Networks

Universidade Estadual de Campinas (UNICAMP)
2015-2024

University of California, San Diego
2023

National Council for Scientific and Technological Development
2017

Fernanda Crunfli Victor Corasolla Carregari Flávio P. Veras Lucas Scárdua Silva Mateus Henrique Nogueira and 83 more André Saraiva Leão Marcelo Antunes Pedro Henrique Vendramini Aline Gazzola Fragnani Valença Caroline Brandão‐Teles Giuliana S. Zuccoli Guilherme Reis‐de‐Oliveira Lícia C. Silva-Costa Verônica M. Saia‐Cereda Bradley J. Smith Ana Campos Codo Gabriela Fabiano de Souza Stéfanie Primon Muraro Pierina Lorencini Parise Daniel A. Toledo-Teixeira Ícaro Maia Santos de Castro Bruno Marcel Silva de Melo Glaucia M. Almeida Egidi Mayara Silva Firmino Isadora Marques Paiva Bruna Manuella Souza Silva Rafaela Mano Guimarães Niele Dias Mendes Raíssa L. Ludwig Gabriel Palermo Ruiz Thiago L. Knittel Gustavo Gastão Davanzo Jaqueline Aline Gerhardt Patrícia Brito Rodrigues Julia Forato Mariene R. Amorim Natália S. Brunetti Matheus Cavalheiro Martini Maíra Nilson Benatti Sabrina Setembre Batah Li Siyuan Rafael Batista João Ítalo Karmann Aventurato Mariana Rabelo de Brito Maria Julia Mendes Beatriz Amorim Da Costa Marina K. M. Alvim José Roberto da Silva Lívia Liviane Damião Iêda Maria Pereira de Sousa Elessandra Dias da Rocha Solange Maria Gonçalves Luiz H. Lopes da Silva Vanessa Bettini Brunno Machado de Campos Guilherme Ludwig Lucas Tavares Marjorie Cornejo Pontelli Rosa Maria Mendes Viana Ronaldo B. Martins André Schwambach Vieira José C. Alves‐Filho Eurico Arruda Guilherme Gozzoli Podolsky Gondim Marcelo Volpon Santos Luciano Neder André Damásio Stevens K. Rehen Marco Aurélio Ramirez Vinolo Carolina Demarchi Munhoz Paulo Louzada‐Júnior Renê Donizeti Ribeiro de Oliveira Fernando Q. Cunha Helder I. Nakaya Thaís Mauad Amaro Nunes Duarte‐Neto Luiz Fernando Ferraz da Silva Marisa Dolhnikoff Paulo Hilário Nascimento Saldiva Alessandro S. Farias Fernando Cendes Pedro M. Moraes‐Vieira Alexandre Todorovic Fabro Adriano Sebollela José Luiz Proença-Módena Clarissa Lin Yasuda Marcelo A. Mori Thiago M. Cunha Daniel Martins‐de‐Souza

Although increasing evidence confirms neuropsychiatric manifestations associated mainly with severe COVID-19 infection, long-term dysfunction (recently characterized as part of "long COVID-19" syndrome) has been frequently observed after mild infection. We show the spectrum cerebral impact acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ranging from alterations in mildly infected individuals (orbitofrontal cortical atrophy, neurocognitive impairment, excessive fatigue and anxiety...

10.1073/pnas.2200960119 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2022-08-11

Phosphorylation of α-synuclein at the serine-129 site (α-syn Ser129P) is an established pathologic hallmark synucleinopathies and a therapeutic target. In physiologic states, only fraction α-syn phosphorylated this site, most studies have focused on roles post-translational modification. We found that unlike wild-type (WT) α-syn, which widely expressed throughout brain, overall pattern Ser129P restricted, suggesting intrinsic regulation. Surprisingly, preventing blocked activity-dependent...

10.1016/j.neuron.2023.11.020 article EN cc-by Neuron 2023-12-01

The limited access to functional human brain tissue has led the development of stem cell-based alternative models. differentiation pluripotent cells into cerebral organoids with self-organized architecture created novel opportunities study early stages formation. Here we applied state-of-the-art label-free shotgun proteomics compare proteome cell-derived fetal brain. We identified 3,073 proteins associated different developmental stages, from neural progenitors neurons, astrocytes, or...

10.3389/fcell.2019.00303 article EN cc-by Frontiers in Cell and Developmental Biology 2019-11-28

Abstract Astrocytes play a critical role in the development and homeostasis of central nervous system (CNS). Astrocyte dysfunction results several neurological degenerative diseases. However, major challenge to our understanding astrocyte physiology pathology is restriction studies animal models, human post-mortem brain tissues, or samples obtained from invasive surgical procedures. Here, we report protocol generate functional astrocytes cerebral organoids derived pluripotent stem cells. The...

10.1038/srep45091 article EN cc-by Scientific Reports 2017-03-27
Fernanda Crunfli Victor Corasolla Carregari Flávio P. Veras Pedro Henrique Vendramini Aline Gazzola Fragnani Valença and 81 more André Saraiva Leão Marcelo Antunes Caroline Brandão‐Teles Giuliana S. Zuccoli Guilherme Reis‐de‐Oliveira Lícia C. Silva-Costa Verônica M. Saia‐Cereda Bradley J. Smith Ana Campos Codo Gabriela Fabiano de Souza Stéfanie Primon Muraro Pierina Lorencini Parise Daniel A. Toledo-Teixeira Ícaro Maia Santos de Castro Bruno Marcel Silva de Melo Glaucia M. Almeida Egidi Mayara Silva Firmino Isadora Marques Paiva Bruna Manuella Souza Silva Rafaela Mano Guimarães Niele Dias Mendes Raissa G. Ludwig Gabriel Palermo Ruiz Thiago L. Knittel Gustavo Gastão Davanzo Jaqueline Aline Gerhardt Patrícia Brito Rodrigues Julia Forato Mariene R. Amorim Natália S. Brunetti Matheus Cavalheiro Martini Maíra Nilson Benatti Sabrina Setembre Batah Li Siyuan Rafael Batista João Lucas Scárdua Silva Mateus Henrique Nogueira Ítalo Karmann Aventurato Mariana Rabelo de Brito Marina K. M. Alvim José Roberto da Silva Lívia Liviane Damião Iêda Maria Pereira de Sousa Elessandra Dias da Rocha Solange Maria Gonçalves Luiz Henrique Lopes da Silva Vanessa Bettini Brunno Machado de Campos Guilherme Ludwig Lucas Tavares Marjorie Cornejo Pontelli Rosa Maria Mendes Viana Ronaldo B. Martins André Schwambach Vieira José C. Alves‐Filho Eurico Arruda Guilherme G. Podolski-Gondim Marcelo Volpon Santos Luciano Neder Fernando Cendes Paulo Louzada‐Júnior Renê Donizeti Ribeiro de Oliveira Fernando Q. Cunha André Damásio Marco Aurélio Ramirez Vinolo Carolina Demarchi Munhoz Stevens K. Rehen Helder I. Nakaya Thaís Mauad Amaro Nunes Duarte‐Neto Luiz Fernando Ferraz da Silva Marisa Dolhnikoff Paulo Hilário Nascimento Saldiva Alessandro S. Farias Pedro M. Moraes‐Vieira Alexandre Todorovic Fabro Adriano Sebollela José Luiz Proença-Módena Clarissa Lin Yasuda Marcelo A. Mori Thiago M. Cunha Daniel Martins‐de‐Souza

Abstract Although increasing evidence confirms neuropsychiatric manifestations associated mainly with severe COVID-19 infection, the long-term dysfunction has been frequently observed after mild infection. Here we show spectrum of cerebral impact SARS-CoV-2 infection ranging from alterations in mildly infected individuals (orbitofrontal cortical atrophy, neurocognitive impairment, excessive fatigue and anxiety symptoms) to acute damage confirmed brain tissue samples extracted orbitofrontal...

10.1101/2020.10.09.20207464 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2020-10-13
Fernanda Crunfli Victor Corasolla Carregari Flávio P. Veras Pedro Henrique Vendramini Aline Gazzola Fragnani Valença and 70 more André Saraiva Leão Marcelo Antunes Caroline Brandão‐Teles Giuliana S. Zuccoli Guilherme Reis‐de‐Oliveira Lícia C. Silva-Costa Verônica M. Saia‐Cereda Ana Campos Codo Pierina Lorencini Parise Daniel A. Toledo-Teixeira Gabriela Fabiano de Souza Stéfanie Primon Muraro Bruno Marcel Silva de Melo Glaucia M. Almeida Egidi Mayara Silva Firmino Isadora Marques Paiva Bruna Manuella Souza Silva Raissa G. Ludwig Gabriel Palermo Ruiz Thiago L. Knittel Gustavo Gastão Davanzo Jaqueline Aline Gerhardt Patrícia Brito Rodrigues Julia Forato Mariene R. Amorim Natália S. Brunetti Matheus Cavalheiro Martini Maíra Nilson Benatti Sabrina Setembre Batah Li Siyuan Rafael Batista João Lucas Scárdua Silva Mateus Henrique Nogueira Ítalo Karmann Aventurato Mariana Rabelo de Brito Marina K. M. Alvim José Roberto da Silva Lívia Liviane Damião Maria Ercilia de Paula Castilho Stefano Iêda Maria Pereira de Sousa Elessandra Dias da Rocha Solange Maria Gonçalves Luiz Henrique Lopes da Silva Vanessa Bettini Brunno Machado de Campos Guilherme Ludwing Rosa Maria Mendes Viana Ronaldo B. Martins André Schwambach Vieira José C. Alves‐Filho Eurico Arruda Adriano Sebollela Fernando Cendes Fernando Q. Cunha André Damásio Marco Aurélio Ramirez Vinolo Carolina Demarchi Munhoz Stevens K. Rehen Thaís Mauad Amaro Nunes Duarte‐Neto Luiz Fernando Ferraz da Silva Marisa Dolhnikoff Paulo Hilário Nascimento Saldiva Alexandre Todorovic Fabro Alessandro S. Farias Pedro M. Moraes‐Vieira José Luiz Proença-Módena Clarissa Lin Yasuda Marcelo A. Mori Thiago M. Cunha Daniel Martins‐de‐Souza

Abstract COVID-19 patients may exhibit neuropsychiatric and neurological symptoms. We found that anxiety cognitive impairment are manifested by 28-56% of SARS-CoV-2-infected individuals with mild respiratory symptoms associated altered cerebral cortical thickness. Using an independent cohort, we histopathological signs brain damage in 25% who died COVID-19. All the affected tissues exhibited foci SARS-CoV-2 infection replication, particularly astrocytes. Infection neural stem cell-derived...

10.21203/rs.3.rs-104944/v1 preprint EN cc-by Research Square (Research Square) 2020-11-13

Abstract Background Schizophrenia is a complex and severe neuropsychiatric disorder, with wide range of debilitating symptoms. Several aspects its multifactorial complexity are still unknown, some accepted to be an early developmental deficiency more specifically neurodevelopmental origin. Understanding the timepoints disturbances during neural cell differentiation processes could lead insight into development disorder. In this context, human brain organoids cells differentiated from...

10.1186/s13578-022-00928-x article EN cc-by Cell & Bioscience 2022-12-01

Schizophrenia (SCZ) is a serious neuropsychiatric disorder that manifests through several symptoms from early adulthood. Numerous studies over the last decades have led to significant advances in increasing our understanding of factors involved SCZ. For example, mass spectrometry-based proteomic analysis has provided important insights by uncovering protein dysfunctions inherent Here, we present comprehensive nuclear proteome postmortem brain tissues corpus callosum (CC) and anterior...

10.1159/000477299 article EN Complex Psychiatry 2017-01-01

Abstract The COVID-19 pandemic was initiated by the rapid spread of a SARS-CoV-2 strain. Though mainly classified as respiratory disease, infects multiple tissues throughout human body, leading to wide range symptoms in patients. To better understand how affects proteome from cells with different ontologies, this work generated an infectome atlas 9 cell models, including brain, blood, digestive system, and adipocyte tissue. Our data shows that infection trigger dysregulations on proteins...

10.1038/s41598-024-56328-3 article EN cc-by Scientific Reports 2024-03-28

Two protein post-translational modifications, lysine succinylation and malonylation, are implicated in regulation, glycolysis, energy metabolism. The precursors of these succinyl-CoA malonyl-CoA, key players central metabolic processes. Both modification profiles have been proven to be responsive stimuli, such as hypoxia. As mitochondrial dysfunction dysregulation schizophrenia other psychiatric illnesses, the potential reveal yet another layer regulation can furthermore represent targets...

10.3390/jpm12091408 article EN Journal of Personalized Medicine 2022-08-30

Exosomes are cell-derived nano vesicles that play multiple roles as mediate cellular communication, elimination of undesirable components and transport molecules such RNAs proteins.Misfolded proteins associated to the development pathologies may be also transported by exosomes.This study aims perform a quantitative proteome analysis exosomes collected from cell cultures derived patients with schizophrenia mentally healthy controls, in order find differentially expressed possibly disease.

10.19146/pibic-2016-50741 article EN Anais do Congresso de Iniciação Científica da Unicamp 2016-10-14

Schizophrenia (SCZ) is a chronic and mental disorder characterized by the presence of positive, negative cognitive symptons.Although molecular mechanisms involved in SCZ still unknow, there dysfunction on energy metabolism cellular signaling.To clarify potential linking between these pathways, we enriched three compartments carried out bottom up proteomics annalysis to find proteins related pathophysiology disease.

10.19146/pibic-2017-78035 article EN Anais do Congresso de Iniciação Científica da Unicamp 2017-10-21

A number of basic and translational studies have clearly indicated the vital role glia in brain function pathophysiological mechanisms neuropsychiatric disorders, including schizophrenia. The difficulty on studying molecular basis glial cells vivo, led to development animal models, which are considered gold standard this type understanding. However, inherent difficulties establishing these models for psychiatric disorders simplicity vitro especially given recent advances stem cell-based...

10.1093/schbul/sby014.034 article EN cc-by Schizophrenia Bulletin 2018-04-01
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