Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability.
The 6 matches
- [1] § Glucocorticoid Modulation in Human Neural in vitro Models › Integrative Analysis of Global Effects of DEX ↔ volcano.py, lines 90–105 · score 0.80 · PIK3R1, HIF3A, TSC22D3, CHST15, LIFR, RASSF4
- [2] § Glucocorticoid Modulation in Human Neural in vitro Models › Neural Progenitors › Exposure Duration on Glucocorticoid Responses ↔ correlation_matrix.py, lines 36–68 · score 0.76 · Dony_FOK4, Dony_409b, Babaniyi_H9, Babaniyi_H1, correlation, Cruceanu
- [3] § Glucocorticoid Modulation in Human Neural in vitro Models › Neural Progenitors › Exposure Duration on Glucocorticoid Responses ↔ scatter.py, lines 14–32 · score 0.62 · Babaniyi_H9, Babaniyi_H1, log2FC, Scatter, fok4, Cruceanu
- [4] § Glucocorticoid Modulation in Human Neural in vitro Models › Neural Progenitors › Exposure Duration on Glucocorticoid Responses ↔ correlation_matrix.py, lines 36–68 · score 0.56 · Babaniyi_H9, Babaniyi_H1, Correlation, Krontira, Dony, models
- [5] § Glucocorticoid Modulation in Human Neural in vitro Models › Integrative Analysis of Global Effects of DEX ↔ correlation_matrix.py, lines 25–34 · score 0.52 · log2 fold change, b2, H1, H9, matrices, neurons
- [6] § Glucocorticoid Modulation in Human Neural in vitro Models › Integrative Analysis of Global Effects of DEX ↔ heatmap.py, lines 90–99 · score 0.51 · functional pathways, regulated genes, heatmap, enriched
Paper
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The authors' code
Python · 119 lines · 4.5 KB · no license · 3 matches
- import os
- import pandas as pd
- import seaborn as sns
- import matplotlib.pyplot as plt
- # =========================================================
- # CONFIGURATION & PATHS
- # =========================================================
- base_path = "data"
- results_path = "results"
- # Ensure the results directory exists
- if not os.path.exists(results_path):
- os.makedirs(results_path)
- # Input files mapping
- files = {
- "babaniyi_H1": "babaniyih1.xlsx",
- "babaniyi_H9": "babaniyih9.xlsx",
- "cruceanu_dn": "cruceanu_dn.xlsx",
- "dony": "donysemfc.xlsx",
- "krontira_dn": "krontira_dn.xlsx"
- }
- # Metadata for gene columns and Fold Change columns
- meta = {
- "babaniyi_H1": ("hgnc_symbol", ["log2FoldChange"]),
- "babaniyi_H9": ("hgnc_symbol", ["log2FoldChange"]),
- "cruceanu_dn": ("gene", ["log2FC"]),
- "dony": ("gene", ["log2FC_Line409b2", "log2FC_LineFOK4"]),
- "krontira_dn": ("gene", ["log2FoldChange"]),
- }
- dony_models = ["ChP", "Ex.Neurons", "Imm.ChP", "Inh.Neurons", "RGS5Neurons"]
- # =========================================================
- # PROCESSING FUNCTIONS
- # =========================================================
- def expand_long_format_and_count(df, gene_col, fc_cols, tag):
- """Filters, cleans, and prepares the data for correlation."""
- if tag == "cruceanu_dn" and "model" in df.columns:
- df = df[df["model"].str.strip().str.upper() == "NEURONS"]
- print(f"📌 Cruceanu filtered for 'Neurons', {df.shape[0]} genes.")
- elif tag == "dony" and "model" in df.columns:
- df = df[df["model"].isin(dony_models)]
- print(f"📌 Dony filtered for models {dony_models}, {df.shape[0]} genes.")
- df = df[[gene_col] + fc_cols].copy()
- df.columns = ["gene"] + fc_cols
- df[fc_cols] = df[fc_cols].apply(pd.to_numeric, errors='coerce')
- df = df[df[fc_cols].notna().any(axis=1)].copy()
- df["gene"] = df["gene"].astype(str).str.upper().str.strip()
- long_frames = []
- counts = {}
- for col in fc_cols:
- col_name = (
- "Dony_409b" if col == "log2FC_Line409b2" else
- "Dony_FOK4" if col == "log2FC_LineFOK4" else
- "Babaniyi_H9" if tag == "babaniyi_H9" else
- "Babaniyi_H1" if tag == "babaniyi_H1" else
- "Krontira" if tag == "krontira_dn" else
- "Cruceanu" if tag == "cruceanu_dn" else tag
- )
- subset = df[["gene", col]].dropna()
- long_frames.append(subset.rename(columns={col: "logFC"}).assign(dataset=col_name))
- counts[col_name] = subset.shape[0]
- return pd.concat(long_frames, ignore_index=True), counts
- # =========================================================
- # DATA LOADING & MERGING
- # =========================================================
- frames = []
- counts_dict = {}
- for tag, fname in files.items():
- gene_col, fc_cols = meta[tag]
- path = os.path.join(base_path, fname)
- # Reading Excel files from the /data folder
- df = pd.read_excel(path, engine="openpyxl")
- expanded_df, counts = expand_long_format_and_count(df, gene_col, fc_cols, tag)
- frames.append(expanded_df)
- counts_dict.update(counts)
- # Gene counts summary
- counts_df = pd.DataFrame(list(counts_dict.items()), columns=["Dataset", "Num_genes"])
- print("\n📌 Number of genes considered per dataset/lineage:")
- print(counts_df)
- # Concatenate all data into a wide matrix
- full_df = pd.concat(frames, ignore_index=True)
- wide_df = full_df.pivot_table(index='gene', columns='dataset', values='logFC', aggfunc='first')
- # =========================================================
- # STATISTICAL ANALYSIS: PEARSON CORRELATION
- # =========================================================
- corr_matrix = wide_df.corr(method='pearson')
- print("\n📌 Pearson Correlation Matrix:")
- print(corr_matrix)
- # =========================================================
- # EXPORTING RESULTS
- # =========================================================
- # Save Correlation Matrix to Excel
- corr_out_path = os.path.join(results_path, "acute_vs_chronic_correlation.xlsx")
- corr_matrix.to_excel(corr_out_path)
- print(f"\n✓ Correlation matrix saved to: {corr_out_path}")
- # Save Correlation Heatmap to PNG
- heatmap_out_path = os.path.join(results_path, "acute_vs_chronic_heatmap.png")
- plt.figure(figsize=(8,6))
- sns.heatmap(corr_matrix, annot=True, fmt=".2f", cmap="coolwarm", square=True)
- plt.tight_layout()
- plt.savefig(heatmap_out_path, dpi=600)
- plt.show()
- print(f"✓ Heatmap saved to: {heatmap_out_path}")
correlation_matrix.py at commit 018ac94, no license · at the source
Overview
Abstract
Glucocorticoids are major regulators of human neural development and stress adaptation, yet their transcriptional effects across experimental paradigms remain poorly integrated. This review synthesizes evidence from 13 studies employing human induced pluripotent stem cell (hiPSC)-derived neural models exposed to cortisol or dexamethasone, including neural progenitors, neurons, astrocytes, and brain organoids. When available, transcriptomic datasets from these studies were reanalyzed under standardized criteria to directly compare acute and chronic GC exposure. This comparative approach revealed that GCs modulate shared pathways related to neurogenesis, cytoskeletal organization, immune signaling, and stress response, while the duration of exposure critically shapes the underlying transcriptional architecture. Acute stimulation predominantly upregulated canonical GR targets such as FKBP5, ZBTB16, and TSC22D3 involved in early stress response and feedback control, whereas chronic exposure induced sustained remodeling of genes including MT2A, RASFAF4, and DPYSL5 linked to oxidative stress regulation and neuronal structure. A conserved downregulated core comprising NFIA, NFIB, and CCL2 was shared across paradigms, reflecting persistent suppression of glial differentiation and inflammatory signaling. Together, these findings delineate distinct yet convergent transcriptional programs governed by GC exposure, providing mechanistic insight into how temporal dynamics of glucocorticoid signaling may contribute to altered neurodevelopmental trajectories and increased vulnerability to stress-related psychiatric disorders.
Supplementary Information: The online version contains supplementary material available at 10.1007/
Reproduced under the paper's license (CC BY), from the paper cited above.
Repository
Its files are read in the Code ↔ Paper reader above, with 6 matches between paragraphs and lines of code.
eloizadalmolin/DEX_neural_models
018ac94d28883b84f1615628d3ffefde1b2fb008, 15 January 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
5 files
- correlation_matrix.py, Python, 119 lines, 3 matches
- heatmap.py, Python, 105 lines, 1 match
- scatter.py, Python, 153 lines, 1 match
- volcano.py, Python, 181 lines, 1 match
- README.md, Text, 38 lines
The paper's code and data availability statement is in the Data section.
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Data
No dataset and no data link were found in the paper.
Data Availability
The datasets reanalyzed in this study were obtained from publicly available repositories cited in the reviewed articles. All processed data and original Python scripts used for comparative transcriptomic integration, including functional enrichment and correlation analyses, are openly available in the GitHub repository: (https://
Reproduced under the paper's license (CC BY), from the paper cited above.
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Version 2, 28 September 2026
- Publisher: n/a → Springer Science+Business Media
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 6 keywords, 9 MeSH terms, 1 funder, 92 references.
Cite
This paper
Dal Molin, E. A., Kaster, M. P., & Nascimento, J. M. (2026). Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability. Molecular neurobiology, 63(1), 748. https://
BibTeX
@article{dalmolin2026glu
author = {Dal Molin, Eloiza Adriane and Kaster, Manuella Pinto and Nascimento, Juliana Minardi},
title = {{Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability}},
journal = {Molecular neurobiology},
year = {2026},
month = jul,
volume = {63},
number = {1},
pages = {748},
publisher = {Springer Science+Business Media},
issn = {0893-7648},
doi = {10.1007/
url = {https://
pmid = {42412256},
pmcid = {PMC13341972}
}
RIS
TY - JOUR
AU - Dal Molin, Eloiza Adriane
AU - Kaster, Manuella Pinto
AU - Nascimento, Juliana Minardi
TI - Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability
T2 - Molecular neurobiology
J2 - Mol Neurobiol
PY - 2026
DA - 2026/
VL - 63
IS - 1
SP - 748
SN - 0893-7648
PB - Springer Science+Business Media
DO - 10.1007/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1007/
"type": "article-journal",
"title": "Glucocorticoid Signaling in PSC-Derived Neural Systems to Elucidate Mechanisms of Stress-Induced Psychiatric Vulnerability",
"container-title": "Molecular neurobiology",
"author": [
{
"family": "Dal Molin",
"given": "Eloiza Adriane"
},
{
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"given": "Manuella Pinto"
},
{
"family": "Nascimento",
"given": "Juliana Minardi"
}
],
"container-title-short":
"volume": "63",
"issue": "1",
"page": "748",
"DOI": "10.1007/
"PMID": "42412256",
"PMCID": "PMC13341972",
"ISSN": "0893-7648",
"publisher": "Springer Science+Business Media",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
7,
7
]
]
}
}
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