Megan K. Rommelfanger

ORCID: 0000-0003-3071-7419
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About
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Research Areas
  • Hematopoietic Stem Cell Transplantation
  • Reproductive Biology and Fertility
  • Immune Cell Function and Interaction
  • Renal and related cancers
  • T-cell and B-cell Immunology
  • Birth, Development, and Health
  • Single-cell and spatial transcriptomics
  • Gene Regulatory Network Analysis

University of Southern California
2021-2023

Abstract Increasing evidence links metabolism, protein synthesis, and growth signaling to impairments in the function of hematopoietic stem progenitor cells (HSPCs) during aging. The Lin28b/Hmga2 pathway controls tissue development, postnatal downregulation this limits self-renewal adult vs fetal (HSCs). Igf2bp2 is an RNA binding downstream Lin28b/Hmga2, which regulates messenger stability translation. role HSC aging unknown. In study, analysis wild-type knockout mice showed that oxidative...

10.1182/blood.2021012197 article EN cc-by-nc-nd Blood 2022-03-01

Cells do not make fate decisions independently. Arguably, every cell-fate decision occurs in response to environmental signals. In many cases, cell-cell communication alters the dynamics of internal gene regulatory network a cell initiate transitions, yet models rarely take this into account. Here, we have developed multiscale perspective study granulocyte-monocyte versus megakaryocyte-erythrocyte decisions. This transition is dictated by GATA1-PU.1 network: classical example bistable...

10.1242/dev.199779 article EN cc-by Development 2021-12-15

Inference of gene regulatory networks (GRNs) can reveal cell state transitions from single-cell genomics data. However, obstacles to temporal inference snapshot data are difficult overcome. Single-nuclei multiomics offer means bridge this gap and derive information using joint measurements expression chromatin accessibility in the same single cells. We developed popInfer infer that characterize lineage-specific dynamic Benchmarking against alternative methods for GRN inference, we showed...

10.1101/2023.04.18.537360 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2023-04-20

Abstract Mammalian organs exhibit distinct physiology, disease susceptibility and injury responses between the sexes. In mouse kidney, sexually dimorphic gene activity maps predominantly to proximal tubule (PT) segments. Bulk RNA-seq data demonstrated sex differences were established from 4 8 weeks after birth under gonadal control. Hormone injection studies genetic removal of androgen estrogen receptors receptor (AR) mediated regulation in PT cells as regulatory mechanism. Interestingly,...

10.1101/2023.05.06.539585 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-05-06
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