Neuropeptidomic Analysis of a Genetically Defined Cell Type in Mouse Brain and Pituitary.
Neuropeptidomic Analysis of a Genetically Defined Cell Type in Mouse Brain and Pituitary.
复制标题
小鼠脑和垂体中遗传定义的细胞类型的神经肽分析。
DOI:
10.1016/j.chembiol.2020.11.003
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发表时间:
2021-01-21
影响因子:
8.6
通讯作者:
Devi LA
中科院分区:
文献类型:
--
作者:
Fricker LD;Tashima AK;Fakira AK;Hochgeschwender U;Wetsel WC;Devi LA
Neuropeptides and peptide hormones are important cell-cell signaling molecules that mediate many physiological processes. Unlike classical neurotransmitters, peptides undergo cell-type-specific post-translational modifications that affect their biological activity. To enable the identification of the peptide repertoire of a genetically-defined cell-type, we generated mice with a conditional disruption of the gene for carboxypeptidase E (Cpe), an essential neuropeptide-processing enzyme. The loss of Cpe leads to accumulation of neuropeptide precursors containing C-terminal basic residues which serve as tags for affinity-purification. The purified peptides are subsequently identified using quantitative peptidomics, thereby revealing the specific forms of neuropeptides in cells with the disrupted Cpe gene. To validate the method, we used mice expressing Cre recombinase under the proopiomelanocortin (Pomc) promoter and analyzed hypothalamic and pituitary extracts, detecting peptides derived from proopiomelanocortin (as expected) and also proSAAS in POMC neurons. This technique enables the analyses of specific forms of peptides in any Cre-expressing cell-type. We report a method to identify neuropeptides in specific cell-types, using mice with a conditional deletion of carboxypeptidase E. It was validated by deleting CPE in proopiomelanocortin cells. Surprisingly, these mice have greatly reduced levels of the anorexigenic peptide α-MSH but are not obese.
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影响因子:
3.5
作者:
Anderson EJ;Çakir I;Carrington SJ;Cone RD;Ghamari-Langroudi M;Gillyard T;Gimenez LE;Litt MJ
通讯作者:
Litt MJ
影响因子:
8.8
作者:
Ding, Cherlyn;Magkos, Faidon
通讯作者:
Magkos, Faidon
影响因子:
4.1
作者:
DAVIDSON, HW;HUTTON, JC
通讯作者:
HUTTON, JC
影响因子:
4.4
作者:
Bora, Adriana;Annangudi, Suresh P.;Millet, Larry J.;Rubakhin, Stanislav S.;Forbes, Andrew J.;Kelleher, Neil L.;Gillette, Martha U.;Sweedler, Jonathan V.
通讯作者:
Sweedler, Jonathan V.
影响因子:
46.9
作者:
Krogager TP;Ernst RJ;Elliott TS;Calo L;Beránek V;Ciabatti E;Spillantini MG;Tripodi M;Hastings MH;Chin JW
通讯作者:
Chin JW