Sung Min Han

Sung Min Han, Ph.D.

BMS Graduate Co-Coordinator

Department: Department of Physiology and Aging
Business Phone: (352) 273-5682
Business Email: han.s@ufl.edu

About Sung Min Han

Dr. Han completed his undergraduate education in Biotechnology in the Republic of Korea in the year 2000. Following that, he served in the Republic of Korea Air Force for three years. From 2001 to 2003, he pursued his master’s degree under the mentorship of Dr. Hyeon-Sook Koo at Yonsei University in South Korea. During this time, Dr. Han conducted research on the role of mitochondria in aging, using the nematode C. elegans as a genetic and in vivo model organism. In 2012, Dr. Han completed his Ph.D. training under the guidance of Dr. Michael Miller at the University of Alabama at Birmingham Medical School. During his Ph.D. program, he continued his investigation into novel signaling mechanisms that connect abnormal mitochondrial function to the mechanisms of amyotrophic lateral sclerosis, a neurodegenerative disorder characterized by the progressive loss of motor neurons. Following his training in neurodegenerative disorders, Dr. Han developed a keen interest in understanding how the nervous system can restore its function after injury. To pursue this interest, he joined Dr. Marc Hammarlund’s lab at Yale University to delve into the molecular and cellular mechanisms that underlie axon regeneration after neuronal injury. In 2018, Dr. Han became an Assistant Professor at the University of Florida. He currently serves as the Course Director for GMS6893 – Clinical and Translational Science Seminar Series, GMS6622 – Mitochondrial Biology in Aging and Disease, and GMS6771 – Clinical Neuroscience of Aging.

Additional Positions:
BMS Graduate Co-Coordinator
2023 – Current ·

Teaching Profile

Courses Taught
2020-2024
GMS6893 Clinical and Translational Science Seminar Series
2020-2024
GMS6622 Mitochondrial Biology in Aging and Disease
2021-2024
GMS6771 Clinical Neuroscience of Aging
2022
GMS6485 Population Based Research on Aging
2023-2024
GMS6491 Journal Club in Physiology
2023-2024
GMS7979 Advanced Research
2024
GMS6472 Fundamentals of Physiology and Functional Genomics II
2024
GMS6473 Fundamentals of Physiology and Functional Genomics III
2024
GMS6471 Fundamentals of Physiology and Functional Genomics I

Research Profile

My long-term research goal is to gain a comprehensive understanding of two key aspects: (i) how the nervous system maintains its function and structural integrity throughout an organism’s lifespan, and (ii) how these processes impact the overall aging and health of the organism.

At present, my research objectives are centered around investigating the following key areas: i) Exploring how aging neurons regulate mitochondrial dynamics and localization in response to localized demands and injury. ii) Investigating the role of mitochondria in controlling nuclear gene expression under specific conditions, with a focus on aging and injury. iii) Examining how mitochondria respond to environmental stressors and their influence on the aging process and overall organismal health. iv) Understanding how stress on mitochondria within the nervous system can impact an organism’s lifespan and healthspan.

To address these research questions, we employ the nematode C. elegans as a powerful genetic and in vivo model system, allowing us to delve into these complex issues.

Open Researcher and Contributor ID (ORCID)

0000-0001-7442-754X

Areas of Interest
  • Aging
  • C. elegans
  • Genetics
  • Mitochondria
  • Motor Neuron Disease
  • Nerve regeneration

Publications

2023
frpr-18, a neuropeptide receptor, regulates organismal lifespan and stress tolerance in C. elegans.
microPublication biology. 2023 [DOI] 10.17912/micropub.biology.000840. [PMID] 37383174.
2023
Melatonin protects against cadmium-induced oxidative stress via mitochondrial STAT3 signaling in human prostate stromal cells.
Communications biology. 6(1) [DOI] 10.1038/s42003-023-04533-7. [PMID] 36750754.
2023
The role of mitochondria in the recovery of neurons after injury
Neural Regeneration Research. 18(2):317-318 [DOI] 10.4103/1673-5374.343907. [PMID] 35900413.
2021
A novel role of the mitochondrial iron-sulfur cluster assembly protein ISCU-1/ISCU in longevity and stress response.
GeroScience. 43(2):691-707 [DOI] 10.1007/s11357-021-00327-z. [PMID] 33527323.
2021
Comparative toxicities of BPA, BPS, BPF, and TMBPF in the nematode Caenorhabditis elegans and mammalian fibroblast cells
Toxicology. 461 [DOI] 10.1016/j.tox.2021.152924.
2021
Distinct temporal actions of different types of unfolded protein responses during aging.
Journal of cellular physiology. 236(7):5069-5079 [DOI] 10.1002/jcp.30215. [PMID] 33345326.
2021
Function of Mitogen-Activated Protein Kinases in Hepatic Inflammation.
Journal of cellular signaling. 2(3):172-180 [PMID] 34557866.
2021
Iron homeostasis and organismal aging.
Ageing research reviews. 72 [DOI] 10.1016/j.arr.2021.101510. [PMID] 34767974.
2020
Editorial: Germline Development: From Germline Stem Cells to Gametes
Frontiers in Cell and Developmental Biology. 8 [DOI] 10.3389/fcell.2020.00650. [PMID] 32850795.
2020
Innovations in Geroscience to enhance mobility in older adults.
Experimental gerontology. 142 [DOI] 10.1016/j.exger.2020.111123. [PMID] 33191210.
2020
The stress-responsive gene GDPGP1/mcp-1 regulates neuronal glycogen metabolism and survival.
The Journal of cell biology. 219(2) [DOI] 10.1083/jcb.201807127. [PMID] 31968056.
2017
The C. elegans VAPB homolog VPR-1 is a permissive signal for gonad development.
Development (Cambridge, England). 144(12):2187-2199 [DOI] 10.1242/dev.152207. [PMID] 28634273.
2017
The secreted MSP domain of C. elegans VAPB homolog VPR-1 patterns the adult striated muscle mitochondrial reticulum via SMN-1.
Development (Cambridge, England). 144(12):2175-2186 [DOI] 10.1242/dev.152025. [PMID] 28634272.
2016
Mitochondria Localize to Injured Axons to Support Regeneration.
Neuron. 92(6):1308-1323 [DOI] 10.1016/j.neuron.2016.11.025. [PMID] 28009276.
2015
RNA ligation in neurons by RtcB inhibits axon regeneration.
Proceedings of the National Academy of Sciences of the United States of America. 112(27):8451-6 [DOI] 10.1073/pnas.1502948112. [PMID] 26100902.
2014
The RtcB RNA ligase is an essential component of the metazoan unfolded protein response.
EMBO reports. 15(12):1278-85 [DOI] 10.15252/embr.201439531. [PMID] 25366321.
2013
VAPB/ALS8 MSP ligands regulate striated muscle energy metabolism critical for adult survival in caenorhabditis elegans.
PLoS genetics. 9(9) [DOI] 10.1371/journal.pgen.1003738. [PMID] 24039594.
2012
Secreted VAPB/ALS8 major sperm protein domains modulate mitochondrial localization and morphology via growth cone guidance receptors.
Developmental cell. 22(2):348-62 [DOI] 10.1016/j.devcel.2011.12.009. [PMID] 22264801.
2010
MSP hormonal control of the oocyte MAP kinase cascade and reactive oxygen species signaling.
Developmental biology. 342(1):96-107 [DOI] 10.1016/j.ydbio.2010.03.026. [PMID] 20380830.
2010
Sperm and oocyte communication mechanisms controlling C. elegans fertility.
Developmental dynamics : an official publication of the American Association of Anatomists. 239(5):1265-81 [DOI] 10.1002/dvdy.22202. [PMID] 20034089.
2009
DIC-1 over-expression enhances respiratory activity in Caenorhabditis elegans by promoting mitochondrial cristae formation.
Genes to cells : devoted to molecular & cellular mechanisms. 14(3):319-27 [DOI] 10.1111/j.1365-2443.2008.01276.x. [PMID] 19210547.
2008
The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors.
Cell. 133(6):963-77 [DOI] 10.1016/j.cell.2008.04.039. [PMID] 18555774.
2006
Deleted in cancer 1 (DICE1) is an essential protein controlling the topology of the inner mitochondrial membrane in C. elegans.
Development (Cambridge, England). 133(18):3597-606 [PMID] 16914495.
2003
Caenorhabditis elegans dna-2 is involved in DNA repair and is essential for germ-line development.
FEBS letters. 555(2):250-6 [PMID] 14644423.
10.3726/978-3-653-04533-8/10
Inactive DOIs. [DOI] 10.3726/978-3-653-04533-8/10.

Grants

Dec 2023 ACTIVE
Exploring the Systemic Regulation of Organismal Longevity and Health through Individual Neuron Mitochondrial Stress
Role: Principal Investigator
Funding: AMER FEDN FOR AGING RES
Apr 2023 ACTIVE
The role and regulation of mitochondrial localization in mature neurons.
Role: Principal Investigator
Funding: NATL INST OF HLTH NIA
Sep 2021 – Feb 2023
Identifying genes that regulate mitochondrial positioning at the synapse during aging
Role: Principal Investigator
Funding: AMER FEDN FOR AGING RES
Sep 2020 – Aug 2022
Understanding the role of mitochondria in the age-related decline in axon regeneration
Role: Principal Investigator
Funding: NATL INST OF HLTH NIA
Jul 2019 – Jun 2023
Identifying genes that regulate mitochondrial positioning at the synapse during aging
Role: Principal Investigator
Funding: AMER FEDN FOR AGING RES
Apr 2017 – Mar 2022
University of Florida Claude D. Pepper Older Americans Independence Center (OAIC)
Role: Project Manager
Funding: NATL INST OF HLTH NIA

Education

Postdoctoral Fellow
2018 · Yale University
PhD in Cell Biology
2012 · University of Alabama at Birmingham
Masters in Biochemistry
2003 · Yonsei University
Bachelors of Science
2000 · Chung-Ang University

Contact Details

Phones:
Business:
(352) 273-5682
Emails:
Business:
han.s@ufl.edu
Addresses:
Business Mailing:
PO Box 100274
1345 CENTER DR
GAINESVILLE FL 32610
Business Street:
1345 Center Drive
Med Sci Bldg, Rm MG-43A
Gainesville FL 32610