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Int J Biol Sci 2026; 22(4):2121-2123. doi:10.7150/ijbs.129515 This issue Cite

Commentary

Spatial Pharmacology: Redefining Organelle Contact Sites as Therapeutic Targets

Minjeong Ko^#, Jiho You^#, Eunwoo Cho, Ho Jeong Kwon

Chemical Genomics Leader Research Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
^# These authors contributed equally to this work.

✉ Corresponding author: Ho Jeong Kwon, kwonhjac.kr

Received 2025-12-5; Accepted 2026-1-12; Published 2026-1-27

Commentary-article in Int J Biol Sci, Volume 22, 731

Inter-organelle communication has emerged as a key regulator of cellular homeostasis and disease pathology [1]. Although organelles were once viewed as self-contained compartments, emerging evidence has reframed organelle membrane contact sites (MCSs) as molecularly diverse signaling hubs that coordinate ion exchange, lipid metabolism, and stress responses. Notably, recent studies published in the International Journal of Biological Sciences have contributed to shifting this perspective by highlighting mitochondria-associated membranes (MAMs) as pharmacologically responsive interfaces implicated in neurodegenerative and metabolic disorders [2-4]. Chen et al. showed that dietary vanadium exposure remodels the hepatic MAM proteome, disrupting glucose homeostasis and promoting ferroptosis [3], while He et al. demonstrated that omega-3 polyunsaturated fatty acids restore MAM abundance and support spermatogenesis [4]. Together, these findings point to a broader conceptual shift in which MCSs are viewed not as passive structural contacts but as dynamic, druggable interfaces, bringing their small-molecule therapeutic potential into clearer focus.

Here, we use the term “spatial pharmacology” to describe therapeutic strategies that modulate organelle connectivity rather than individual molecular activities. The implications of this concept extend well beyond the MAM. Recent studies show that diverse organelle contact sites function as key regulatory hubs and can be modulated pharmacologically. In early Alzheimer's disease, Blarcamesine (ANAVEX2-73), an agonist of the Sigma-1 receptor localized at the MAM, demonstrated notable outcomes in clinical trials for Alzheimer's disease (NCT03790709) [5]. The flavonoid derivative LW-213 enhanced ER-lysosome interactions through direct binding to lysosomal protein LIMP2, thereby triggering lethal ER stress and suppressing acute myeloid leukemia progression [6]. Another natural product, tangeretin, exhibited protective mechanisms against Amyloid beta (Aβ) toxicity by modulating mitochondria-lysosome contacts [7]. At the ER-plasma membrane contact sites, the TAT-DP-2 peptide provided neuroprotection in an ischemic stroke model by disrupting the Kv2.1-VAPA interaction [8]. Together, these examples illustrate a growing paradigm of “spatial pharmacology,” wherein targeted modulation of organelle connectivity acts as a distinct therapeutic mechanism (Figure 1).

MCS-centered pharmacology is emerging as a new direction in drug discovery, connecting systems-level organelle biology with therapeutics ranging from small molecules to peptides. The main challenge now is achieving precise spatial and temporal control so that these strategies can be applied effectively in clinical settings. Because MCSs are structurally complex and highly dynamic, systemic drugs alone may not provide sufficient specificity, and additional approaches will be synergetic for more accurate manipulation of cellular architecture. To this end, emerging technologies such as organelle-targeting nanoparticles and optogenetic tools represent a promising future direction. Nanoparticles can be engineered with specific physicochemical properties to exploit membrane potential or pH gradients, allowing them to enrich payloads at distinct organelle sites [9]. This targeted subcellular delivery allows organelle crosstalk to be modulated precisely, in ways that conventional whole-cell drug exposure cannot achieve. Optogenetic/chemogenetic tools that enable graded control of protein associations, such as small-molecule-activated binary association (SAMBA) systems, can also offer the ability to program the timing and duration of contact formation [10]. Furthermore, bridging structural understanding with pharmacological intervention will be essential to translate MCS-targeting strategies into clinically actionable therapies.

 Figure 1 

Translating organelle contact site biology into spatial pharmacology and therapeutic intervention. Understanding of organelle membrane contact sites (MCSs) has progressed from structural characterization to therapeutic exploration. Small molecules and peptides that modulate ER-mitochondria or ER-lysosome contact dynamics can reprogram inter-organelle signaling and metabolic coordination, offering new opportunities for therapeutic intervention in neurodegenerative, cancer, and metabolic disorders.

Overall, these advances make it increasingly possible to control organelle contacts in a precise and predictable way. By adjusting how organelles connect and communicate, we can begin to treat these contact sites not just as structural features of the cell, but as real therapeutic targets. This idea, that cell function can be modulated by adjusting how organelles connect, captures the core of spatial pharmacology and suggests a new direction for future drug development.

Acknowledgements

This work was supported in part by grants from the National Research Foundation of Korea, funded by the government of the Republic of Korea (2021R1A3B1077371) and by the Brain Korea 21 Plus Project. Additional support was provided by the Institute of Convergence Science (ICONS), Yonsei University. This research also received support from the Regional Innovation System & Education (RISE) through the Seoul RISE Center, funded by the Ministry of Education (MOE) and the Seoul Metropolitan Government (2025-RISE-01-022-05).

Competing Interests

The authors have declared that no competing interest exists.

References

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Corresponding author: Ho Jeong Kwon, kwonhjac.kr

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